ليست عنوان مقالات لاتين Synthesis of 2,4-dihydroxyquinazolines using carbon dioxide in the presence of DBU under mild conditions Synthesis of a complementary dimer from mono(imidazolyl)-substituted cobalt(II) porphyrin as a new artificial T-form hemoglobin

<< مقالات لاتين >>

<< بر اساس عنوان >>

1

Synthesis of 2,4-dihydroxyquinazolines using carbon dioxide in the presence of DBU under mild conditions

2

Synthesis of 2,4-dimethyl-6-oxo-2,4-heptadienoic acid derivatives from 2,4,6-trimethylpyrylium salts

3

Synthesis of 2,4-dinitrophenylhydrazine loaded sodium dodecyl sulfate-coated magnetite nanoparticles for adsorption of Hg(II) ions from an aqueous solution

4

Synthesis of 2,4-disubstituted 3-chlorofurans and the effect of the chlorine substituent in furan Diels–Alder reactions

5

Synthesis of 2,5-anhydro-(β-d-glucopyranosyluronate)- and (α-l-idopyranosyluronate)-d-mannitol hexa-O-sulfonate hepta sodium salt

6

Synthesis of 2,5-bis{(diethyl-3′-indolyl)methyl}furan and its N,N′-dimetallated complexes (lithium, sodium and potassium): X-ray crystal structures of 2,5-bis{(diethyl-3′-indolyl)methyl}furan and the polymeric tetrahydrofuran adduct of the dilithiated com

7

Synthesis of 2,5-di(2-thienyl)-1H-pyrrole N-linked with conjugated bridges

8

Synthesis of 2,5-diaryloxazoles through van Leusen reaction and copper-mediated direct arylation

9

Synthesis of 2,5-Dideoxy-5-Substituted Pyrimidine Nucleosides via Intramolecular Glycosylation

10

Synthesis of 2,5-diethynyl substituted oxepins from trans-1,4-diethynylcyclohexa-2,5-diene-1,4-diols

11

Synthesis of 2,5-difunctionalised-3,3-dimethylpiperidines via ω-halogenated imines

12

Synthesis of 2,5-dihalothiazole-4-carboxylates

13

Synthesis of 2,5-dihydrobenzo[b]oxepines and 5,6-dihydro-2H-benzo[b]oxocines based on a ‘[3+3] cyclization-olefin-metathesis’ strategy

14

Synthesis of 2,5-dihydrobenzo[b]oxepins and 5,6-dihydro-2H-benzo[b]oxocines based on [3+3] cyclizations of 1,3-bis(silyl enol ethers)

15

Synthesis of 2,5-disubstituted-3-cyanoindoles

16

Synthesis of 2,5-thiazole butanoic acids as potent and selective αvβ3 integrin receptor antagonists with improved oral pharmacokinetic properties

17

Synthesis of 2,6,10,14,18,22-hexaazaspiro[11.11]tricosane, the first example of a spiro aza crown derived from 2,2-bis(aminomethyl)propane-1,3-diamine

18

Synthesis of 2,6-bis(4R-trialkylsiloxymethyloxazolinyl)pyridines and their use in catalytic asymmetric 1,3-dipolar cycloaddition reactions of nitrones and activated alkenes

19

Synthesis of 2,6-cis-disubstituted 4-methylenetetrahydropyrans by oxy-Michael addition

20

Synthesis of 2,6-di(pyrazol-1-yl)-4-bromomethylpyridine, and its conversion to other 2,6-di(pyrazol-1-yl)pyridines substituted at the pyridine ring

21

Synthesis of 2,6-diaryl-1,2-dihydropyridines through a 6π-electrocyclization of N-sulfonylazatrienes

22

Synthesis of 2,6-diaryl-3-(trifluoromethyl)pyridines by regioselective Suzuki–Miyaura reactions of 2,6-dichloro-3-(trifluoromethyl)pyridine

23

Synthesis of 2,6-diaryl-4,4-diphenyldithienosiloles and their luminescent properties

24

Synthesis of 2,6-dichlorobenzonitrile from 2,6-dichlorotoluene by gas phase ammoxidation over VPO catalysts

25

Synthesis of 2,6-dimethyl-9-aryl-9-phosphabicyclo[3.3.1]nonanes: their application to asymmetric synthesis of chiral tetrahydroquinolines and relatives

26

Synthesis of 2,6-dimethylnaphthalene by methylation of methylnaphthalene on various medium and large-pore zeolite catalysts Original Research Article

27

Synthesis of 2,6-dioxabicyclo[3.3.0]octenes by tandem ring-rearrangement/cross metathesis

28

Synthesis of 2,6-dioxatricyclo[3.3.1.03,7]nonanes by intramolecular haloetherification and/or transannular hydroxycyclization of alkenes in [4+3]-cycloadducts

29

Synthesis of 2,6-Dioxo-(1H,3H)-9-N-ribitylpurine and 2,6-Dioxo-(1H,3H)-8-aza-9-N-ribitylpurine as inhibitors of lumazine synthase and riboflavin synthase Original Research Article

30

Synthesis of 2,6-disubstituted dihydropyrans via an efficient BiBr3-initiated three component, one-pot cascade

31

Synthesis of 2,6-disubstituted morpholines through regioselective oxiranes ring opening by tosylamide under PTC conditions

32

Synthesis of 2,6-disubstituted piperidine alkaloids from ladybird beetles Calvia 10-guttata and Calvia 14-guttata

33

Synthesis of 2,6-disubstituted pyrido[2,3-b][1,4]oxazines

34

Synthesis of 2,6-disubstituted-7,8-dihydro-6H-pyrano[2,3-6]pyrazines

35

Synthesis of 2,9-dialkylated phenanthro[1,2-b:8,7-b′]dithiophenes via cross-coupling reactions and sequential Lewis acid-catalyzed regioselective cycloaromatization of epoxide

36

Synthesis of 2-[(2-pyridyl)amino]ethyl β-d-lactosaminide and evaluation of its acceptor ability for sialyltransferase: a comparison with 4-methylumbelliferyl and dansyl β-d-lactosaminide Original Research Article

37

Synthesis of 2-[(Z)-1-hydropolyfluoro-1-alkenyl]-4H-3,1-benzoxazin-4-ones

38

Synthesis of 2-[18F]fluoro-image-tyrosine via regiospecific fluoro-de-stannylation

39

Synthesis of 2-[3-(7-Chloro-quinolin-4-ylamino)-alkyl]-1-(substituted phenyl)-2,3,4,9-tetrahydro-1H-β-carbolines as a new class of antimalarial agents

40

Synthesis of 2-[3,5-substituted pyrazol-1-yl]-4,6-trisubstituted triazine derivatives as antimalarial agents

41

Synthesis of 2-[4-(substituted benzylidene)-5-Oxo- 4,5-dihydro-oxazol-2-ylmethyl]-isoindole-1,3-dione Derivatives as Novel Potential Antimicrobial Agents

42

Synthesis of 2-[5-amino-2,3-dihydro-4H-imidazol-4-ylidene]malononitriles

43

Synthesis of 2-[6-(2,4-Dinitrophenoxy)hexyl]oxiranecarboxylic acid: A selective carnitine palmitoyltransferase-1 inhibitor Original Research Article

44

Synthesis of 2’-(5-Chloro-2-Hydroxybenzylidene) Benzenesulfanohydrazide Schiff Base and its Anti-Ulcer Activity in Ethanol-Induced Gastric Mucosal Lesions in Rats

45

Synthesis of 2′,3′-dideoxy-2′-monofluoromethyl azanucleosides Original Research Article

46

Synthesis of 2′,3′-dideoxy-3′,4′-dihydroxymethyl substituted pyrimidine nucleoside analogues

47

Synthesis of 2′,3′-dideoxy-3′-C-(hydroxymethyl)-4′-thiopentofuranosyl nucleosides as potential antiviral agent

48

Synthesis of 2′,3′-dideoxy-3′-fluoro-l-ribonucleosides as potential antiviral agents from d-sorbitol Original Research Article

49

Synthesis of 2′,3′-dideoxy-6′,6′-difluoro-3′-azanucleosides

50

Synthesis of 2′,3′-dideoxy-6′-fluorocarbocyclic nucleosides via Reformatskii–Claisen rearrangement

51

Synthesis of 2′,3′-dideoxynucleosides via C–S bond cleavage: N-glycosylation of 2,3-dideoxy-1-[(2-pyridylmethyl)thio]glycoside

52

Synthesis of 2′,3′-dihydrosolanesyl analogues of β-d-arabinofuranosyl-1-monophosphoryldecaprenol with promising antimycobacterial activity

53

Synthesis of 2′,5′-oligoadenylate analogs containing an adenine acyclonucleoside and their ability to activate human RNase L

54

Synthesis of 2′-aminoalkyl-1-benzylisoquinoline derivatives and medium sized ring analogues with mu opiod receptor binding activities

55

Synthesis of 2′-C-methyl-branched isonucleosides

56

Synthesis of 2′-C-α-difluoromethylarauridine and its 3′-O-phosphoramidite incorporation into a hammerhead ribozyme

57

Synthesis of 2′-dealkylmumbaistatin

58

Synthesis of 2′-deoxy-2′-fluororibo- and 2′-deoxy-2′,2′-difluororibonucleosides derived from 6-(het)aryl-7-deazapurines

59

Synthesis of 2′-deoxyibosylnucleosides using new 2′-deoxyribosyltransferase microorganism producers

60

Synthesis of 2′-deoxyuridine 5′-(α,β-imido)triphosphate: a substrate analogue and potent inhibitor of dUTPase Original Research Article

61

Synthesis of 2′-hydrazine oligonucleotides and their efficient conjugation with aldehydes and 1,3-diketones

62

Synthesis of 2′-O,3′-O bicyclic adenosine analogues using ring closing metathesis

63

Synthesis of 2′-O-[2-[(N,N-dialkylamino)oxy]ethyl]-modified oligonucleotides: hybridization affinity, resistance to nuclease, and protein binding characteristics

64

Synthesis of 2′-O-modified adenosine building blocks and application for RNA interference Original Research Article

65

Synthesis of 2′-O-α-d-ribofuranosyladenosine, monomeric unit of poly(ADP–ribose)

66

Synthesis of 2′-paclitaxel methyl 2-glucopyranosyl succinate for specific targeted delivery to cancer cells

67

Synthesis of 2′-β-C-methyl toyocamycin and sangivamycin analogues as potential HCV inhibitors

68

Synthesis of 2′-β-C-methyl-neplanocin derivatives as anti-HCV agents

69

Synthesis of 2″-acylamido derivatives of 2″-amino-5,2″-dideoxy-5-epi-5-fluorodibekacin and a study on the structures of 5-fluorinated dibekacin analogs by 13C NMR

70

Synthesis of 2″-oxidized derivatives of 5-deoxy-5-epi-5-fluoro-dibekacin and -arbekacin, and study on structure-chemical shift relationships of urethane(or amide)-type NH protons in synthetic intermediates

71

Synthesis of 21,21-Difluoro-3β-hydroxy-20-methylpregna-5,20-diene and 5,16,20-Triene as potential inhibitors of steroid C17(20) lyase Original Research Article

72

Synthesis of 21,31-O-(propane-1,2-diyl)- and 21,31-O-(3-hydroxypropane-1,2-diyl)-cyclomaltoheptaose

73

Synthesis of 21-nor-22-oxa-1α,25-dihydroxyvitamin D3 derivatives in quest of a drug with low calcemic activity

74

Synthesis of 21-oxoporphyrin building blocks and energy donor appended systems

75

Synthesis of 21-thia and 21-oxaporphyrin building blocks and boron–dipyrrin appended systems

76

Synthesis of 22-oxaspiro[4.5]decane CD-ring modified analogs of 1α,25-dihydroxyvitamin D3

77

Synthesis of 25-aminosterols, new antifungal agents

78

Synthesis of 26,27-bisnorcastasterone analogs and analysis of conformation–activity relationship for brassinolide-like activity Original Research Article

79

Synthesis of 26-hydroxy-22-oxocholestanic frameworks from diosgenin and hecogenin and their in vitro antiproliferative and apoptotic activity on human cervical cancer CaSki cells Original Research Article

80

Synthesis of 28-19F-amphotericin B methyl ester

81

Synthesis of 2-acetamido-1,2-dideoxy-d-galacto-nojirimycin [DGJNAc] from d-glucuronolactone: the first sub-micromolar inhibitor of α-N-acetylgalactosaminidases

82

Synthesis of 2-acetamido-2-deoxy-5-thio-β-d-altropyranose

83

Synthesis of 2-acetamido-2-deoxy-β-d-glucopyranosyl-(1 → 2)-α-d-mannopyranosyl (1 → 6)-β-d-mannopyranosyl-(1 → 4)-2-acetamido-2-deoxy-d-glucopyranose. Acceptor-substrate recognition by N-acetylglucosaminyltransferase-V (GnT-V)

84

Synthesis of 2-acetamido-3-O-acetyl-2-deoxy-d-mannose phosphoramidites

85

Synthesis of 2-acetoxy[5]helicene by sequential double aromatic oxy-Cope rearrangement

86

Synthesis of 2-acylamino-2-deoxy-d-glucofuranoses and their transformation into hex-2-enofuranoses

87

Synthesis of 2-acylindole-3-acetic acids: a novel base-mediated indole synthesis

88

Synthesis of 2-alkoxy-8-hydroxyadenylpeptides: Towards synthetic epitope-based vaccines

89

Synthesis of 2-alkoxymethyl-3-trifluoromethyl-1,4-naphthoquinones

90

Synthesis of 2-alkyl (and aryl)-1-aryl-2-propen-1-ones via m-CPBA mediated oxidation of γ-(benzotriazol-1-yl)allylic selenides

91

Synthesis of 2-alkyl-2-arylcyanoacetates via CuI/sodium picolinate-catalyzed direct arylation of α-substituted cyanoacetates

92

Synthesis of 2-alkyl-3-aryl-substituted quinuclidines as novel dopamine transporter inhibitors

93

Synthesis of 2-alkylidene-cycloalkane-1,3-diols via enantioselective intramolecular carbolithiation

94

Synthesis of 2-alkylidenetetrahydrofurans by Ru-catalyzed regio- and stereoselective codimerization of dihydrofurans with ,(alpha),(beta)-unsaturated esters

95

Synthesis of 2-alkynylquinolines from 2-chloro and 2,4-dichloroquinoline via Pd/C-catalyzed coupling reaction in water

96

Synthesis of 2-amido, 2-amino, and 2-azido derivatives of the nitrogen analogue of the naturally occurring glycosidase inhibitor salacinol and their inhibitory activities against O-GlcNAcase and NagZ enzymes Original Research Article

97

Synthesis of 2-amido-3-hydroxypyridin-4(1H)-ones: novel iron chelators with enhanced pFe3+ values Original Research Article

98

Synthesis of 2-amino-1,3,4-oxadiazoles from isoselenocyanates via cyclodeselenization

99

Synthesis of 2-amino-1,3-dienes by chromium-catalyzed addition of silylated propargyl bromides to imines

100

Synthesis of 2-amino-1,3-diols incorporating the cyclobutane ring

101

Synthesis of 2-amino-2,4-anhydro-3-O-(2-tetrahydropyranyl)-psicofuranose: a versatile intermediate for S-type locked nucleosides

102

Synthesis of 2-Amino-3,5-dicarbonitrile-6-thiopyridines Using Silica-bonded N-Propyldiethylenetriamine as a Heterogeneous Solid Base Catalyst

103

Synthesis of 2-amino-3-cyano-4H-chromen-4-ylphosphonates and 2-amino-4H-chromenes catalyzed by tetramethylguanidine

104

Synthesis of 2-amino-3-hydroxy-4-substituted pyridines via regioselective metalation of 3-(1-ethylpropyl)-[1,3]oxazolo[4,5-b]pyridin-2(3H)-one and application to corticotropin releasing factor1 receptor ligands

105

Synthesis of 2-amino-4-(4-methoxyphenyl)-1,3-thiazole coatedmagnetic nanoparticles: A potential antibacterial compound

106

Synthesis of 2-amino-4-(7-azaindol-3-yl)pyrimidines as cyclin dependent kinase 1 (CDK1) inhibitors

107

Synthesis of 2-amino-4,6-diarylnicotininitriles using 3-propyldiethylenetriamine-silica as a recyclable solid base catalyst

108

Synthesis of 2-amino-4H-chromene derivatives by three-component condensation using an amino acid as a suitable and useful catalyst under solvent-free and thermally conditions

109

Synthesis of 2-Amino-4H-chromene Derivatives under Solvent-Free Condition Using MOF-5

110

Synthesis of 2-amino-4H-pyran derivatives in aqueous media with nano-SnO2 as recyclable catalyst

111

Synthesis of 2Amino4hydroxy1HPyrrole3Carbonitrile from Glycine Under Microwave Irradiation

112

Synthesis of 2-amino-5-alkylidenethiazol-4-ones from ketones, rhodanine, and amines with the aid of re-usable heterogeneous silica-pyridine based catalyst

113

Synthesis of 2-amino-5-chloro-3-(trifluoromethyl)benzenethiol and conversion into 4H-1,4-benzothiazines and their sulfones

114

Synthesis of 2-amino-5-substituted-1,3,4-oxadiazoles using 1,3-dibromo-5,5-dimethylhydantoin as oxidant

115

Synthesis of 2-amino-6-(2-[18F]fluoro-pyridine-4-ylmethoxy)-9-(octyl-β-d-glucosyl)-purine: a novel radioligand for positron emission tomography studies of the O6-methylguanine-DNA methyltransferase (MGMT) status of tumour tissue

116

Synthesis of 2-amino-6-(4-[11C]methoxyphenylthio)-9-[2-(phosphonomethoxy)ethyl]purine bis(2,2,2-trifluoroethyl) ester as a novel potential PET gene reporter probe for HBV and HSV-tk in cancers Original Research Article

117

Synthesis of 2-amino-8-chloro-4-phenyl-5,11-dihydro-6H-pyrido[2,3-a]carbazole-3-carbonitrile: Structural and biological evaluation

118

Synthesis of 2-aminoazulene derivatives. Nucleophilic and palladium-catalyzed amination of 2-substituted azulene

119

Synthesis of 2-aminobenzoxazoles via copper-catalyzed electrophilic amination of benzoxazoles with O-benzoyl hydroxylamines

120

Synthesis of 2-aminocyclopropyl pyrrolidines from glycoaminonitriles

121

Synthesis of 2-aminoethyl-5-carbethoxythiazoles utilizing a Michael-like addition strategy

122

Synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolin-1-ols and their conversion to 7-aryl-9H-6-oxa-5,8-diaza-benzocycloheptenes

123

Synthesis of 2-aryl-1h-benzimidazole derivatives using nano montmorillonite clay as an efficient catalyst

124

Synthesis of 2-aryl1-H-benzo[d]imidazole derivatives using nano montmorillonite clay as an efficient catalyst

125

Synthesis of 2-aryl-2H-[1,2,4]triazoloquinolin-3-one and 2-aryl-2H-[1,2,4]triazoloisoquinolin-3-one derivatives from α-chloroformylarylhydrazines hydrochloride

126

Synthesis of 2-aryl-2H-indazoles by base catalysed reaction of 2-nitrobenzyl triphenylphosphonium bromide and aryl isocyanates

127

Synthesis of 2-aryl-3,3,3-trifluoropropanoic acids using electrochemical carboxylation of (1-bromo-2,2,2-trifluoroethyl)arenes and its application to the synthesis of β,β,β-trifluorinated non-steroidal anti-inflammatory drugs

128

Synthesis of 2-aryl-3-hydroxymethyl-5,5-difluoropiperidines

129

Synthesis of 2-aryl-4-chloropyrroles via ring expansion of 2-aryl-1-chlorocyclopropanecarbaldehydes

130

Synthesis of 2-aryl-4H-pyrano[2,3-b]pyridin-4-ones by a one-pot deprotection–cyclization reaction

131

Synthesis of 2-aryl-6-methyl-5-nitroquinoline derivatives as potential prodrug systems for reductive activation

132

Synthesis of 2-arylacrylic esters from aryl methyl ketones via Wittig reaction/singlet oxygen ene reaction

133

Synthesis of 2-arylbenzimidazoles via microwave Suzuki–Miyaura reaction of unprotected 2-chlorobenzimidazoles

134

Synthesis of 2-arylbenzoxazoles via DDQ promoted oxidative cyclization of phenolic Schiff bases—a solution-phase strategy for library synthesis

135

Synthesis of 2-aryl-imidazo[4,5-d][1,2,3]triazoles from a 4-nitro-imidazol-5-yl phosphoramidate and aryl isocyanates

136

Synthesis of 2-arylpropionic acids by electrocarboxylation of benzylchlorides catalysed by PdCl2(PPh3)2

137

Synthesis of 2-azaspiro[4.4]nonan-1-ones via phosphine-catalysed [3+2]-cycloadditions

138

Synthesis of 2-azidoethyl α-d-mannopyranoside orthogonally protected and selective deprotections

139

Synthesis of 2-benzoyl-4-(2-hydroxybenzoyl)phenols by catalytic domino ‘Michael–retro-Michael–Mukaiyama-aldol’ reactions of 1-aryl-1,3-bis(silyloxy)buta-1,3-dienes with 3-formylchromones

140

Synthesis of 2-benzyl-2H-pyrazole-3,4-diamine dihydrochloride

141

Synthesis of 2-benzylimidazo[2,1-b][1,3]benzothiazoles through palladium-catalyzed heteroannulation of acetylenic compounds

142

Synthesis of 2-boryl-1,3-butadienes from tributylphosphine stabilized zirconacyclopropenes and alkynes

143

Synthesis of 2-bromo-1-aryl-1H-indenes via a Ag(I) promoted domino 2π-electrocyclic ring-opening/4π-electrocyclization reaction of 1,2-diaryl substituted gem-dibromocyclopropanes

144

Synthesis of 2-bromo-1H-indenes via copper-catalyzed intramolecular cross-coupling of gem-dibromoolefins

145

Synthesis of 2-bromo-7-methyl-3,5-dihydro-imidazo[4,5-d]pyridazin-4-one and 3-alkyl-2-bromo-3,5-dihydro-imidazo[4,5-d]pyridazin-4-one and their selective elaboration

146

Synthesis of 2-chloro-1,1-difluoroallyl mesylates through novel rearrangement and CC bond formation by their Pd-catalyzed reaction with diethylzinc

147

Synthesis of 2-chloro-4-nitrophenyl α-l-fucopyranoside: a substrate for α-l-fucosidase (AFU)

148

Synthesis of 2-chloro-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one

149

Synthesis of 2-C-hydroxymethylribofuranosylpurines as potent anti-hepatitis C virus (HCV) agents

150

Synthesis of 2-C-methylerythritols and 2-C-methylthreitols via enantiodivergent Sharpless dihydroxylation of trisubstituted olefins

151

Synthesis of 2-C-trifluoromethyl substituted d-ribose

152

Synthesis of 2-cyano-1,4-cycloheptadiene derivatives via divinylcyclopropane rearrangement and alkylation of novel cycloheptadienyl anion species

153

Synthesis of 2D metal–organic coordination polymers with large internal cavities and their magnetic properties

154

Synthesis of 2D polymeric dicyanamide bridged hexa-coordinated Cu(II) complex: Structural characterization, spectral studies and TDDFT calculation

155

Synthesis of 2-Dehydro-3-epi-20-hydroxyecdysone

156

Synthesis of 2-deoxy cyclic and linear oligosaccharides by oligomerization of monomers Original Research Article

157

Synthesis of 2-deoxy-2-(4-nitroimidazol-1-yl)-d-alditols

158

Synthesis of 2-deoxy-2,3-didehydro-N-acetylneuraminic acid analogues modified at the C-4 and C-9 positions and their behaviour towards sialidase from influenza virus and pig liver membrane Original Research Article

159

Synthesis of 2-Deoxy-2-C-Alkylglucosides of myo-Inositol as possible inhibitors of a N-Deacetylase enzyme in the biosynthesis of mycothiol

160

Synthesis of 2-deoxy-2-fluoro analogs of polyprenyl β-d-arabinofuranosyl phosphates

161

Synthesis of 2-deoxy-2-fluoro and 1,2-ene derivatives of the naturally occurring glycosidase inhibitor, salacinol, and their inhibitory activities against recombinant human maltase glucoamylase

162

Synthesis of 2-deoxy-2-fluoro-glucotropaeolin, a thioglucosidase inhibitor

163

Synthesis of 2-deoxy-2-fluoro-phosphatidylinositol-4,5-bisphosphate and analogues: Probes and modulators of the mammalian PI-PLCS

164

Synthesis of 2-deoxy-d-arabino/lyxo-hexopyranosyl disaccharides Original Research Article

165

Synthesis of 2-deoxy-hexopyranosyl derivatives of uridine as donor substrate analogues for glycosyltransferases

166

Synthesis of 2-deoxy-α-DAH based on diazo chemistry by insertion reactions of 2-diazo-3-deoxy-d-arabino-heptulosonate derivatives mediated by rhodium(II)

167

Synthesis of 2-Diphenylphosphinoyl-2 -Halo Biphenyls Via Suzuki-Miyaura Coupling as Possible Route to Non-Symmetric Biphenyl Phosphines

168

Synthesis of 2-diphenylphosphinoyl-3,5-(diaryl)-3,4-dihydro-2H-thiopyrans by the reaction of a bis[(diphenylphosphinoyl)methyl]sulfide with chalcones

169

Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride

170

Synthesis of 2E,4E,6E,11Z-octadecatetraenoic acid of the Rhizobium leguminosarum biovar viciae Nod factor

171

Synthesis of 2-ethyl-2-hexenal oxime and its flotation performance for copper ore

172

Synthesis of 2-ferrocenylquinoline derivatives and evaluation of their antimalarial activity

173

Synthesis of 2-fluoro and 4-fluoro galactopyranosyl phosphonate analogues of UDP-Gal Original Research Article

174

Synthesis of 2-fluoronoraristeromycin and its inhibitory activity against Plasmodium falciparum S-Adenosyl- -homocysteine hydrolase

175

Synthesis of 2-fluorotetralones by oxidative radical cyclization of α-fluoroacetophenones and olefins

176

Synthesis of 2H-1,2-oxaphosphorin 2-oxides

177

Synthesis of 2H-1,4-benzothiazin-3(4H)-ones and 2H-1,4-benzoselenazin-3(4H)-ones with the aid of samarium(II) iodide

178

Synthesis of 2H-1,5-benzodioxepin and 2,5-dihydro-1,6-benzodioxocin derivatives via ring-closing metathesis reaction

179

Synthesis of 2-halo-2H-azirines

180

Synthesis of 2H-chromenes and 1,2-dihydroquinolines from aryl aldehydes, amines, and alkenylboron compounds

181

Synthesis of 2H-pyrroles by treatment of pyrrolidines with DDQ

182

Synthesis of 2H-pyrroles via the 1,3-dipolar cycloaddition reaction of nitrile ylides with acrylamides

183

Synthesis of 2-hydroxy acid from 2-amino acid by Clostridium butyricum

184

Synthesis of 2-hydroxy-3-indolinones and 3-hydroxy-2-indolinones by anionic cyclization, in situ oxidation and rearrangement

185

Synthesis of 2-hydroxy-3-methylbut-3-enyl substituted coumarins and xanthones as natural products. Application of the Schenck ene reaction of singlet oxygen with ortho-prenylphenol precursors

186

Synthesis of 2-hydroxy-3-substituted naphthoquinones using the Heck reaction

187

Synthesis of 2-imidazolidinylidene propanedinitrile derivatives as stimulators of gastrointestinal motility—III Original Research Article

188

Synthesis of 2-iminothiazoline derivatives by sequential conjugate addition/annulation/ring-opening reactions

189

Synthesis of 2-iodo- and 2-phenyl-[11C]melatonin: potential PET tracers for melatonin binding sites

190

Synthesis of 2-iodo-2-deoxy septanosides from a d-xylose-based oxepine: intramolecular cyclization in the absence of a glycosyl acceptor Original Research Article

191

Synthesis of 2-iodoynamides and regioselective [2+2] cycloadditions with ketene

192

Synthesis of 2-isoxazoline and α-hydroxy ketomethylene dipeptide isosteres Original Research Article

193

Synthesis of 2-mercapto-3-substituted-5,6-dimethylthieno[2,3-d] pyrimidin-4(3H)-ones as new analgesic, anti-inflammatory agents

194

Synthesis of 2-Mercaptobenzimidazole and Some of its Derivatives

195

Synthesis of 2-mesityl-3-methylpyrrole via the Trofimov reaction for a new BODIPY with hindered internal rotation

196

Synthesis of 2-methoxy-2-methyl-3-{6-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]pyridin-3-yl}propanoic acid, a dual PPARα/γ agonist

197

Synthesis of 2-methyl- and 2-methylenecyclobutane amino acids

198

Synthesis of 2-methyl-4-methoxydiphenylamine by palladium catalyzed C–N coupling—high synthetic versatility by use of a flexible catalytic system

199

Synthesis of 2-methylidene-1-silacyclohexanes by intramolecular hydrosilylation

200

Synthesis of 2-methylidene-1-silacyclohexanes from 2,6-dibromohex-1-ene and polyhalosilanes

201

Synthesis of 2-modified aristeromycins and their analogs as potent inhibitors against Plasmodium falciparum S-adenosyl-l-homocysteine hydrolase Original Research Article

202

SYNTHESIS OF 2-MONO- AND 2,7-DISUBSTITUTED-1,8-DIHYDROXY9-ANTHRONES, A NOVEL MEMBER OF THE ANTHRONE CLASS OF ANTIPSORIATIC AGENTS

203

Synthesis of 2-monoacylglycerols and structured triacylglycerols rich in polyunsaturated fatty acids by enzyme catalyzed reactions

204

Synthesis of 2-N-alkyl(aryl)amino-7-nitrobenzothiazoles

205

Synthesis of 2-naphthylacrylamides and 2-naphthylacrylates via homogeneous catalytic carbonylation of 1-iodo-1-naphthylethene derivatives

206

Synthesis of 2-NBDLG, a fluorescent derivative of l-glucosamine; the antipode of d-glucose tracer 2-NBDG

207

Synthesis of 2-N-substituted benzothiazoles via domino condensation-hetero cyclization process, mediated by copper oxide nanoparticles under ligand-free conditions

208

Synthesis of 2-O-(2-iodoethyl)-d-glucose, a stable iodinated analogue of 2-deoxy-2-fluoro-d-glucose

209

Synthesis of 2-O-heteroaroyl taxanes: evaluation of microtubule assembly promotion and cytotoxicity

210

Synthesis of 2-oxazolidinone catalyzed by palladium on charcoal: a novel and highly effective heterogeneous catalytic system for oxidative cyclocarbonylation of β-aminoalcohols and 2-aminophenol

211

Synthesis of 2-oxazolidinones by salen-Co-complexes catalyzed oxidative carbonylation of β-amino alcohols

212

Synthesis of 2-oxazolidones by sulfur-assisted thiocarboxylation with carbon monoxide and oxidative cyclization with molecular oxygen under mild conditions

213

Synthesis of 2-oxazolines and related N-containing heterocycles using [Et2NSF2]BF4 as a cyclodehydration agent

214

Synthesis of 2-oxazolines mediated by N,N′-diisopropylcarbodiimide

215

Synthesis of 2-oxazolines via boron esters of N-(2-hydroxyethyl) amides

216

Synthesis of 2-pentafluorosulfanylnaphthalene

217

Synthesis of 2-phenylethyl acetate in the presence of Yarrowia lipolytica KKP 379 biomass

218

Synthesis of 2-phenylquinoline-based ambipolar molecules containing multiple 1,3,4-oxadiazole spacer groups

219

Synthesis of 2-picolyl functionalized η5-cyclopentadienyl derivatives of rhodium(I) and iridium(I) and preliminary study of their reaction with ruthenium(II) for assembling hetero-bimetallic complexes

220

Synthesis of 2-pyranosyl benzothiazoles, benzimidazoles and benzoxazoles via nucleophilic addition reactions of pyranosyl nitrile oxides

221

Synthesis of 2-pyranylidene or (2-furyl)carbene–chromium complexes from conjugated enyne carbonyl compounds with Cr(CO)5(THF)

222

Synthesis of 2-pyridones as tissue factor VIIa inhibitors

223

Synthesis of 2-pyrolyl-2-hydroxy-2-cyanoacetamide through FeCl3–TBHP mediated hydroxylation of captodative stabilized radical intermediate

224

Synthesis of 2-pyrone-4-carboxaldehydes from acetylene dicarboxaldehyde monoacetal

225

Synthesis of 2S-(2-hydroxyethyl)-3R-hydroxy-4S-(thymin-1-yl or adenin-9-yl)-tetrahydrofuran

226

Synthesis of 2-selenoxoperhydro-1,3-selenazin-4-ones via diselenocarbamate intermediates

227

Synthesis of 2-Substitued Benzimidazoles Using P2O5-SiO2

228

Synthesis of 2-Substitued Benzimidazoles Using P2O5-SiO2

229

Synthesis of 2-substituted -tryptophan-containing peptide derivatives with endothelin receptor antagonist activity

230

Synthesis of 2-substituted 1-benzyl-2,3,4,5-tetrahydro-1-benzazepines by palladium catalysis. Observation of a competitive β-hydride elimination pathway

231

Synthesis of 2-substituted 2H-chromenes using potassium vinyltrifluoroborates

232

Synthesis of 2-substituted 3-ethyl-3H-imidazo[4,5-b]pyridines catalyzed by Al3+-exchanged K10 clay as solid acids

233

Synthesis of 2-substituted bamipine derivatives

234

Synthesis of 2-Substituted Benzimidazoles and Bis-benzimidazoles by Microwave in the Presence of Alumina-Methanesulfonic Acid

235

Synthesis of 2-substituted chromenes via ring-closing metathesis and stable 1-benzopyrylium ions

236

Synthesis of 2-substituted endo-hymenialdisine derivatives

237

Synthesis of 2-substituted indoles by palladium-catalyzed heteroannulation with Pd–NaY zeolite catalysts

238

Synthesis of 2-substituted indoles via a palladium-catalyzed domino Heck reaction and dealkylation

239

Synthesis of 2-substituted piperazines via direct α-lithiation

240

Synthesis of 2-substituted pyrrolidines from nitriles

241

Synthesis of 2-substituted quinones, vitamin K3, and vitamin K1 from p-cresol. BF3·OEt2-catalyzed methyl migration of 4-tert-butyldioxycyclohexadienones

242

Synthesis of 2-substituted-7-azaindoles from 2-amino-3-picolin

243

Synthesis of 2-substituted-benzothiazoles by palladium-catalyzed intramolecular cyclization of o-bromophenylthioureas and o-bromophenylthioamides

244

Synthesis of 2-substituted-pyrrolidinethiourea derivatives and their antagonist effect on vanilloid receptor

245

Synthesis of 2-thioxoimidazolines via reaction of 1-unsubstituted 3-aminoquinoline-2,4-diones with isothiocyanates

246

Synthesis of 2-TIPS-oxazol-5-ylboronic acid pinacol ester: efficient route to 5-(het)aryloxazoles via Suzuki cross-coupling reaction

247

Synthesis of 2-trifluoromethoxyethyl trifluoromethoxyacetate and derived 2-trifluoromethoxyacrylates

248

Synthesis of 2-trifluoromethyl-1(substituted aryl)-4(1H)-quinolones using trifluoroacetamidoyl chlorides

249

Synthesis of 2-trifluoromethylthioacrylate and its derivatives via the Knoevenagel condensation

250

Synthesis of 2-ynamides by direct palladium-catalyzed oxidative aminocarbonylation of alk-1-ynes

251

Synthesis of 2α- and 2β-substituted-14-epi-previtamin D3 and their genomic activity

252

Synthesis of 3- and 5-amino-5-(3)-(pyrrol-2-yl)isoxazoles

253

Synthesis of 3- and 5-endo-(6-Chloro-3-pyridoxy)-methyl-2-azabicyclo[2.2.0]hexane and 3-endo-(6-Chloro-3-pyridoxy)-methyl-2-azabicyclo[2.2.0]hex-5-ene. ABT-594 Analogs

254

Synthesis of 3-((6-methyl-5-oxo-3-thioxo-2,5-dihydro-1,2,4-triazin-4(3H)-yl)imino)indolin-2-one as an Excellent Ionophore to the Construction of a Potentiometric Membrane Sensor for Rapid Determination of Zinc

255

Synthesis of 3-(1H-benzimidazol-2-yl)-5-isoquinolin-4-ylpyrazolo[1,2-b]pyridine, a potent cyclin dependent kinase 1 (CDK1) inhibitor

256

Synthesis of 3-(1H-benzo[d]imidazol-1-yl)isoindolin-1-one derivatives promoted by EtOH–AcOH solvent system

257

Synthesis of 3-(2-deoxy-β-d-ribofuranosyl)pyridin-2-one and 2-amino-6-(N,N-dimethylamino)-9-(2-deoxy-β-d-ribofuranosyl)purine derivatives for an unnatural base pair

258

Synthesis of 3-(2-nitroalkyl) indoles by reaction of 3-(1-arylsulfonylalkyl) indoles with nitroalkanes

259

Synthesis of 3-(2-pyridyl)-2-substituted-quinazolin-4(3H)-ones as new analgesic and anti-inflammatory agents

260

Synthesis of 3-(3,4-dihydroxyphenyl)-propionic acid derivatives by N-coupling of amines using laccase

261

Synthesis of 3-(4-heteroaryl-phenyl)-8-oxabicyclo[3.2.1]octane-2-carboxylic acid methyl esters

262

Synthesis of 3-(alkylamino and anilino)-4-benzyloxycarbonyl-1H-pyrrole-2,5-diones via 5-[(alkylamino and anilino)(cyano)]-2,2-dimethyl-1,3-dioxane-4,6-diones

263

Synthesis of 3-(benzylideneamino)-2-phenyl-5H-imidazo[1,2-b]pyrazole-7-carbonitriles via a four-component condensation reaction

264

Synthesis of 3-(Trifluoromethyl)benzo[c][1,6]naphthyridines from Substituted 4H-Pyran-4-ones via 4-Amino-5-Aryl-2-(trifluoromethyl)pyridines

265

Synthesis of 3-(trifluoromethyl)indeno[2,1-c]pyran-1,9-diones from 4-aryl-3-carbethoxy-6-(trifluoromethyl)-2-pyrones and their reaction with sodium azide leading to new carbostyril derivatives

266

Synthesis of 3-(Trimethoxysilyl)PropylMethacrylateFunctionalized GrapheneOxideBased Mixed MatrixMembrane andItsApplication for O2/N2Separation

267

Synthesis of 3-(α- and β-d-arabinofuranosyl)-6-chloro-1,2,4-triazolo[4,3-b]pyridazine Original Research Article

268

Synthesis of 3, 4-Dihydropyrimidin-2-(1H)-ones Using a Hydrogel as a Green and Reusable Catalyst

269

Synthesis of 3,20-disubstituted chlorophyll-a derivatives and reactivity of the substituents

270

Synthesis of 3,3,3-trifluoroprop-1-enyl compounds from some enolizable aldehydes

271

Synthesis of 3,3,4,4-tetrafluoro-1,2-bis(imino)cyclobutanes: A cyclic version of fluorinated α-diimines

272

Synthesis of 3,3,6,6-Tetraaryl-1,2-Dioxanes via TiO2-catalyzed Photooxygenation of 1,1-Diarylethenes in the Presence of Mg(ClO4)2

273

Synthesis of 3,3′-neotrehalosadiamine and related 1,1′-aminodisaccharides using disarmed, armed, and superarmed building blocks

274

Synthesis of 3,3-bis(difluoramino)octahydro-1,5,7,7-tetranitro-1,5-diazocine (TNFX), a diversified energetic heterocycle

275

Synthesis of 3,3-dimethoxy-2-aryl-2,3-dihydro-1-oxa-cyclopenta[l]phenanthren-2-ols and their conversion to 2(3H)- and 3(2H)-furanones

276

Synthesis of 3,3-disubstituted oxetane building blocks

277

Synthesis of 3,3-disubstituted oxindoles

278

Synthesis of 3,3-disubstituted oxindoles through Pd-catalyzed intramolecular cyanoamidation

279

Synthesis of 3,3-Disubstituted-2,2-bipyridines from 1,10-Phenanthroline-5,6-quinone

280

Synthesis of 3,4,5-trisubstituted indoles via iterative directed lithiation of 1-(triisopropylsilyl)gramines

281

Synthesis of 3,4-diaryl-1-phenyl-4,5-dihydro-1H-pyrazole-5-carbonitriles via 1,3-dipolar cycloaddition reactions

282

Synthesis of 3,4-dihydrobenzo[g]isoquinoline-1(2H)-ones and 3,4-dihydroisoquinoline-1(2H)-ones skeleton via intramolecular electrophilic cyclization

283

Synthesis of 3,4-Dihydropyrano[c]Chromene Derivatives Using Sulfonic Acid Functionalized Silica (SiO2PrSO3H)

284

Synthesis of 3,4-dihydropyridin-2-one derivatives in convergent mode applying bio catalyst vitamin B1 and polymer supported catalyst PEG–SO3H from two different sets of building blocks

285

Synthesis of 3,4-dihydropyrimidin-2(1H)-ones and 1,4-dihydropyridines using ammonium carbonate in water

286

Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones Catalyzed by Nafion-H Under Ultrasound Irradiation and Solvent-Free Conditions

287

Synthesis of 3,4-dihydropyrimidin-2-ones (DHPMs) using mesoporous aluminosilicate (AlKIT-5) catalyst with cage type pore structure

288

Synthesis of 3,4-dihydropyrimidinones by the reaction between β-ketoesters, aromatic aldehydes and urea in the presence of pectin as a hetero polysaccharide catalyst

289

Synthesis of 3,4-Dihydropyrimidinones using Nano γ-Al2O3/BF3/ Fe3O4 as an Efficient Magnetic Nanocatalyst under Solvent-free Conditions

290

Synthesis of 3,4-dihydropyrrolo[2,1-a]isoquinolines based on [3+2] cycloaddition initiated by Rh2(cap)4-catalyzed oxidation

291

Synthesis of 3,4-dihydroquinazolin-4-one: selenium-catalyzed reductive N-heterocyclization of N-(2-nitrobenzoyl)amides with carbon monoxide

292

Synthesis of 3,4-Dihydroquinoxalin-2-Amine, Diazepine-Tetrazole and Benzodiazepine-2-Carboxamide Derivatives with the Aid of H6P2W18O62/Pyridino-Fe3O4

293

Synthesis of 3,4-di-O-acetyl-2,5-anhydro-1,6-dideoxy-1,6-diiodo-d-mannitol. Comparison of NMR spectral results for the solid state and solution with those of the X-ray structural determination

294

Synthesis of 3,4-di-O-acylated glucose-derived furanoid sugar amino acids (Gaa): conformational analysis of a Leu-enkephalin analog containing di-O-myristoylated Gaa

295

Synthesis of 3,4-disubstituted 2(1H)-quinolinones via intramolecular Friedel–Crafts reaction of N-arylamides of Baylis–Hillman adducts

296

Synthesis of 3,4-disubstituted 2,5-dihydrofurans starting from the Baylis–Hillman adducts via consecutive radical cyclization, halolactonization, and decarboxylation strategy

297

Synthesis of 3,4-disubstituted cinnolines by the Pd-catalyzed annulation of 2-iodophenyltriazenes with an internal alkyne

298

Synthesis of 3,4-disubstituted piperidines by ene cyclisation of 4-aza-1,7-dienes

299

Synthesis of 3,4-disubstituted α-methylene-γ-lactones via sonochemical Barbier-type reaction

300

Synthesis of 3,4-fused cycloalkanopyrroles by 1,3-dipolar cycloaddition

301

Synthesis of 3,4-substituted cyclopentenones via an intramolecular Pauson–Khand reaction of NO linked enynes

302

Synthesis of 3,5,6-trisubstituted α-pyrones from Baylis–Hillman adducts

303

Synthesis of 3,5-bis(2-indolyl)pyridine and 3-[(2-indolyl)-5-phenyl]pyridine derivatives as CDK inhibitors and cytotoxic agents Original Research Article

304

Synthesis of 3,5-Diaryl Azoline and [1,4] Diazepine Derivatives via Microwave Irradiation

305

Synthesis of 3,5-diaryl-4-chlorophthalates by [4+2] cycloaddition of 1-ethoxy-2-chloro-1,3-bis(trimethylsilyloxy)-1,3-diene with dimethyl acetylenedicarboxylate and subsequent site-selective Suzuki–Miyaura reactions

306

Synthesis of 3,5-diazabicyclo [5.1.0] octenes. A new platform to mimic glycosidase transition states

307

Synthesis of 3,5-difunctionalized 1-methyl-1H-pyrazolo[3,4-b]pyridines involving palladium-mediated coupling reactions

308

Synthesis of 3,5-dioxoalkanoates, 3,5-dioxopimelates and 2,4-dioxoadipates by acylation of 1,3-bis-silyl enol ethers

309

Synthesis of 3,5-disubstituted 1,2,4-oxadiazoles and their behavior of liquid crystallines

310

Synthesis of 3,5-disubstituted 1,2,4-oxadiazoles as peptidomimetic building blocks

311

Synthesis of 3,5-disubstituted 1,2,4-oxadiazoles using ionic liquid-phase organic synthesis (IoLiPOS) methodology

312

Synthesis of 3,5-disubstituted-1,2,4-oxadiazoles using tetrabutylammonium fluoride as a mild and efficient catalyst

313

Synthesis of 3,5-lutidine from propionaldehyde over modified ZSM-5 catalysts Original Research Article

314

Synthesis of 3,6-bicyclolides: A novel class of macrolide antibiotics

315

Synthesis of 3,6-bis[H-Tyr/H-Dmt-NH(CH2)m,n]-2(1H)pyrazinone derivatives: Function of alkyl chain length on opioid activity

316

Synthesis of 3,6-branched arabinogalactan-type tetra- and hexasaccharides for characterization of monoclonal antibodies Original Research Article

317

Synthesis of 3,6-branched oligomannoside fragments of the mannan from Candida albicans cell wall corresponding to the antigenic factor 4 Original Research Article

318

Synthesis of 3,6-diazabicyclo[3.1.1]heptanes as novel ligands for neuronal nicotinic acetylcholine receptors

319

Synthesis of 3,6-diazabicyclo[3.1.1]heptanes as novel ligands for the opioid receptors Original Research Article

320

Synthesis of 3,6-dihydro-2H-pyran-2-ones via cationic palladium(II) complex-catalyzed tandem [2+2] cycloaddition-allylic rearrangement of ketene with α,β-unsaturated aldehydes and ketones

321

Synthesis of 3,6-dioxa-Δ7-4-trifluoromethyl perfluorooctyl trifluoromethyl sulfonimide: bis[(perfluoroalkyl)sulfonyl] superacid monomer and polymer

322

Synthesis of 3,6-epoxy[1,5]dioxocines from 2-hydroxyaromatic benzaldehydes

323

Synthesis of 3,7-dihydroimidazo[1,2a]pyrazine-3-ones and their chemiluminescent properties

324

Synthesis of 3,8,13,18-tetrachloro-2,7,12,17-tetramethoxyporphyrin

325

Synthesis of 3,8,9-trisubstituted-1,7,9-triaza-fluorene-6-carboxylic acid derivatives as a new class of insulin secretagogues Original Research Article

326

Synthesis of 3/8-carbonylated chlorophyll derivatives and regiodependent reductivity of their carbonyl substituents

327

Synthesis of 3-[(N-carboalkoxy)ethylamino]-indazole-dione derivatives and their biological activities on human liver carbonyl reductase Original Research Article

328

Synthesis of 3-[2-(1,3-butadienyl)]-1H-indoles en route to murrapanine analogue

329

Synthesis of 3-[4′-(p-chlorophenyl)-thiazol-2′-yl]-2-[(substituted azetidinone/thiazolidinone)-aminomethyl]-6-bromoquinazolin-4-ones as anti-inflammatory agent Original Research Article

330

Synthesis of 3′-, 4′- and 6′-deoxy and other analogues of d-glucosaminylphosphatidylinositol

331

Synthesis of 3′,4′-epoxynoraristeromycin analogs for molecular labeling probe of S-adenosyl-l-homocysteine hydrolase Original Research Article

332

Synthesis of 3′-allylindoline spirobenzopyrans derived from 3-allyl-3H-indoles

333

Synthesis of 3′-azido-4′-ethynyl-3′,5′-dideoxy-5′-norarabinouridine: a new anti-HIV nucleoside analogue

334

Synthesis of 3′-C-substituted thymidine derivatives by free-radical techniques: scope and limitations

335

Synthesis of 3′-deoxy-3′-C-methyl nucleoside derivatives Original Research Article

336

Synthesis of 3′-deoxy-3′-C-methyl-β-d-ribonucleoside analogs

337

Synthesis of 3′-O-phosphonomethyl nucleosides with an adenine base moiety

338

Synthesis of 30 wt%BAS/Si3N4 composite by spark plasma sintering

339

Synthesis of 32-nitro-chlorophyll-a derivatives and their electronic absorption/emission data

340

Synthesis of 32-substituted bacteriochlorophyll-d analogs and their self-aggregation in a nonpolar organic solvent

341

Synthesis of 35–40 mers of RNA oligomers from unblocked monomers. A simple approach to the RNA world

342

Synthesis of 3a,4-dihydro-3H-[1]benzopyrano[4,3-c]isoxazoles, displaying combined 5-HT uptake inhibiting and α2-adrenoceptor antagonistic activities. Part 2: Further exploration on the cinnamyl moiety

343

Synthesis of 3a,4-dihydro-3H-[1]benzopyrano[4,3-c]isoxazoles, displaying combined 5-HT uptake inhibiting and α2-adrenoceptor antagonistic activities: a novel series of potential antidepressants

344

Synthesis of 3-acetamido-1,2,4-tri-O-acetyl-3,5-dideoxy-5-C-[(R)- and (S)-phenylphosphinyl]-α- and -β-d-xylopyranoses

345

Synthesis of 3-acetonyl- and 3-(2-oxoethyl)glutarates

346

Synthesis of 3-acyltetrahydrofurans from formaldehyde acetals of allylic diols

347

Synthesis of 3-alkenyl-2-arylchromones and 2,3-dialkenylchromones via acid-catalysed retro-Michael ring opening of 3-acylchroman-4-ones

348

Synthesis of 3-alkoxycarbonyl-1β-methylcarbapenem using palladium-catalyzed amidation of vinyl halide

349

Synthesis of 3-alkyl naphthalenes as novel estrogen receptor ligands

350

Synthesis of 3-alkyl(Aryl)-4-alkylidenamino-4,5-dihydro-1H-1,2,4-triazol-5-ones and 3-alkyl-4-alkylamino-4,5-dihydro-1H-1,2,4-triazol-5-ones as antitumor agents Original Research Article

351

Synthesis of 3-alkyl-1-isoindolinones by alkylation of a benzotriazolyl substituted N-dimethylamino-phthalimidine

352

Synthesis of 3-alkyl-5-hydroxycyclohex-2-enones via aldolic addition/sulfinate elimination tandem reactions

353

Synthesis of 3-alkylidene-piperidin-4-ones via one-pot cascade transylidation–olefination

354

Synthesis of 3-alkyloxazolidin-2,4-diones using 2-chloroacetamides, carbon dioxide and 1,8-diazabicyclo[5.4.0]undecene (DBU)

355

Synthesis of 3-amido-3-deoxy-β-d-talopyranosides: all-cis-substituted pyranosides as lectin inhibitors

356

SYNTHESIS OF 3-AMINO-1-PHENYL-1H-PYRAZOLE-4, 5-DIONE-4-ARYLHYDRAZONES AS FAST DYES

357

Synthesis of 3-amino-5H-pyrrolo[2,3-e]-1,2,4-triazines by Sonogashira/copper(I)-catalyzed heteroannulation

358

Synthesis of 3-amino-5-methyl-[1,1 -biaryl]-2,4-dicarbonitriles using ZnFe2O4 magnetic nanoparticles

359

Synthesis of 3-aminoaspartic acid derivatives from glycine precursors

360

Synthesis of 3-aminoindole derivatives: combination of Thorpe–Ziegler cyclization and unexpected allylindium-mediated decyanation

361

Synthesis of 3-aminopyrrolidines and piperidines from endocyclic enamine derivatives

362

Synthesis of 3-aminopyrrolidines by cyclization of neutral C-centered α-aminoalkyl radicals

363

Synthesis of 3-aryl substituted benzo[1,2,5]triazepin-4-ones via intramolecular imine formation

364

Synthesis of 3-aryl-3,4-dihydroisocoumarins by regioselective domino ‘[3+3] cyclization/lactonization’ reactions of 1,3-bis-(silyloxy)-1,3-butadienes with 1-hydroxy-5-silyloxy-4-en-3-ones

365

Synthesis of 3-aryl-3-hydroxypyrrolidin-2-ones and 2-benzyl-9b-hydroxy-3,3a,5,9b-tetrahydro-2H-pyrrolo[3,4-c]quinoline-1,4-dione derivatives from the Baylis–Hillman adducts of isatins

366

Synthesis of 3-aryl-4-chalcogen-2H-benzopyrans from 3-iodo-4-chalcogen-2H-benzopyrans using a Suzuki cross-coupling

367

Synthesis of 3-aryl-4-methyl-1,2-benzenedisulfonimides, new chiral Brønsted acids. A combined experimental and theoretical study

368

Synthesis of 3-arylcoumarins through N-heterocyclic carbene catalyzed condensation and annulation of 2-chloro-2-arylacetaldehydes with salicylaldehydes

369

Synthesis of 3-arylcoumarins via Suzuki-cross-coupling reactions of 3-chlorocoumarin

370

Synthesis of 3-arylisocoumarins, including thunberginols A and B, unsymmetrical 3,4-disubstituted isocoumarins, and 3-ylidenephthalides via iodolactonization of methyl 2-ynylbenzoates or the corresponding carboxylic acids

371

Synthesis of 3-Arylpropenyl, 3-Arylpropynyl and 3-Arylpropyl 2-Azetidinones as Cholesterol Absorption Inhibitors: Application of the Palladium-Catalyzed Arylation of Alkenes and Alkynes

372

Synthesis of 3-Aryl-Substituted Tetrahydropyran-4-ones and Tetrahydrothiopyran-4-ones

373

Synthesis of 3-azabicyclo[4.1.0]heptane-1-carboxylic acid

374

Synthesis of 3-azido-3-deoxy-β-d-galactopyranosides Original Research Article

375

Synthesis of 3-benzazepines and azepino[4,5-b]heterocyclic ring systems via intramolecular Friedel–Crafts cyclization

376

Synthesis of 3-benzyl-2-substituted quinoxalines as novel monoamine oxidase A inhibitors

377

Synthesis of 3beta-(4-[18F]Fluoromethylphenyl)- and beta-(2-[18F] Fluoromethylphenyl)tropane-2beta-Carboxylic Acid Methyl Esters: New Ligands for Mapping Brain Dopamine Transporter With Positron Emission Tomography

378

Synthesis of 3-buten-1-ol from 1,4-butanediol over indium oxide Original Research Article

379

Synthesis of 3-C-(6-O-acetyl-2,3,4-tri-O-benzyl-α-d-mannopyranosyl)-1-propene: a caveat

380

Synthesis of 3-C-(methyl β-d-xylofuranosid-3-yl)-5-phenyl-1,2,4-oxadiazole

381

Synthesis of 3-chloroanthranilates from α,γ,γ-trichloro-β-iminoesters

382

Synthesis of 3-C-Spiro Ring Nucleoside Analogues, of Possible Biological Activity

383

Synthesis of 3-cyano-2-fluoropyridines

384

Synthesis of 3-cyclohexylpropyl caffeate from 5-caffeoylquinic acid with consecutive enzymatic conversions in ionic liquid

385

Synthesis of 3D hierarchical Ag microspheres assembled with dendritic morphology

386

Synthesis of 3D hierarchical porous carbon as an electrode material for electric double layer capacitors

387

Synthesis of 3D hierarchical porous carbon as electrode material for electric double layer capacitors

388

Synthesis of 3-deaza-3-nitro-2′-deoxyadenosine Original Research Article

389

Synthesis of 3-deoxy-2,4-di-O-methyl-d-erythro-pentono-1,5-lactone and of its l enantiomer by stereoselective hydrogenation of α, β-unsaturated aldono-1,5-lactones

390

Synthesis of 3-deoxy-2-ulosonic acid KDO and 4-epi-KDN, a highly efficient approach of 3-C homologation by propargylation and oxidation

391

Synthesis of 3-deoxy-3,3-difluoro-d-ribohexose from gem-difluorohomoallyl alcohol

392

Synthesis of 3-Deoxyclarithromycin through Biotransformation of Clarithromycin by Aspergillus niger and its Antibacterial Activity

393

Synthesis of 3-derivatized pyrroles precursors polymers for functionalization with biomolecules toward biosensor devices

394

Synthesis of 3-dimensional mesoporous silica using a di-block copolymer template

395

Synthesis of 3-fluoro-2-(diethoxyphosphoryl)imidazo[1,2-a]pyridine

396

Synthesis of 3-fluorobenzoyl chloride functionalized magnetic sorbent for highly efficient enrichment of perfluorinated compounds from river water samples

397

Synthesis of 3-fluoroimidazo[1,2-a]pyrimidines and 5-fluoroimidazo[2,1-b][1,3]thiazoles via heterocyclization of (N-heteroarylimino)trifluoropyruvates

398

Synthesis of 3-functionalized 3-methylazetidines

399

Synthesis of 3-halo-2,5-disubstituted furans via CuX mediated cyclization–halogenation reactions

400

Synthesis of 3-halo-analogues of HHQ, subsequent cross-coupling and first crystal structure of Pseudomonas quinolone signal (PQS)

401

Synthesis of 3-hexuloses from 1,2:5,6-di-O-isopropylidenehexitols

402

Synthesis of 3H-labeled Efomycine M

403

Synthesis of 3H-labeled N-(3-iodoprop-2E-enyl)-2β-carbomethoxy-3β-(4-methylphenyl)nortropane (PE2I) and its interaction with mice striatal membrane fragments

404

Synthesis of 3H-spiro[benzofuran-2,1′-cyclohexane] derivatives from naturally occurring filifolinol and their classical complement pathway inhibitory activity

405

Synthesis of 3-hydroxyindolin-2-one alkaloids, (±)-donaxaridine and (±)-convolutamydines A and E, through enolization–Claisen rearrangement of 2-allyloxyindolin-3-ones

406

Synthesis of 3I-O and 2I-O-monosubstituted derivatives of per-6-azido-β-cyclodextrin—potential molecular scaffolds Original Research Article

407

Synthesis of 3-iodobenzo[b]thiophenes via iodocyclization/etherification reaction sequence

408

Synthesis of 3-iodothiophenes via iodocyclization of (Z)-thiobutenynes

409

Synthesis of 3-methoxy-9-(3,4,5-trimethoxyphenyl)-6,7-dihydro-5H-benzo[7]annulen-4-ol, a potent antineoplastic benzosuberene derivative for anti-cancer chemotherapy

410

Synthesis of 3-methoxyquinolines via cyclization of 1-isocyano-2-(2-lithio-2-methoxyethenyl)benzenes

411

Synthesis of 3-methoxy-quinoxalin-2-ones from methyl trimethoxyacetate and phenylenediamines

412

Synthesis of 3-methyl- and 3,4-dimethylfurans using alkoxide, thiolate, and phenoxide-mediated cyclization of 4-oxahepta-1,6-diynes bearing sulfur and selenium functional groups

413

Synthesis of 3-methyl-2-cyclohexenones catalyzed by mercury(II) salts and their microwave assisted BiCl3 catalyzed aldol condensations

414

Synthesis of 3-methyl-4-arylmethylene isoxazole-5(4H)-ones by visible light in aqueous ethanol

415

Synthesis of 3-methyleneindan-1-ol scaffold from modified Baylis–Hillman adduct: tandem Pd-catalyzed 5-exo-trig cyclization and iodide ion-assisted formal δ-carbon elimination/decarboxylation

416

Synthesis of 3-methyleneisoindolin-1-ones via palladium-catalyzed C–Cl bond cleavage and cyclocarbonylation of ortho-chloro ketimines

417

Synthesis of 3-Nitro-lH-indole-2-carboxylic Acid Ethyl Ester Derivatives from Baylis-Hillman Adducts

418

Synthesis of 3-O-(β-d-xylopyranosyl-(1→2)-β-d-glucopyranosyl)-3′-O-(β-d-glucopyranosyl)tamarixetin, the putative structure of aescuflavoside A from the seeds of Aesculus chinensis

419

Synthesis of 3-O-acyl/3-benzylidene/3-hydrazone/3-hydrazine/17-carboxyacryloyl ester derivatives of betulinic acid as anti-angiogenic agents

420

Synthesis of 3-O-methylviridicatin analogues with improved anti-TNF-α properties

421

Synthesis of 3-O-sulfoglucuronyl lacto-N-neotetraose 2-aminoethyl glycoside and biotinylated neoglycoconjugates thereof Original Research Article

422

Synthesis of 3-oxagranatane-type alkaloid analogs from carbohydrates

423

Synthesis of 3-Oxa-guaianolides from Santonin

424

Synthesis of 3-oxo oxacycloalkenes by ring closing metathesis

425

Synthesis of 3-oxo-4-benzoyl-1-phenylsuccinimide and its reactions with 1,2- dinucleophiles

426

Synthesis of 3-oxooxa- and 3-oxoazacycloalk-4-enes by ring-closing metathesis. Application to the synthesis of an inhibitor of cathepsin K

427

Synthesis of 3-pentanone from 1-propanol over CeO2–Fe2O3 catalysts Original Research Article

428

Synthesis of 3-Phenyl-2,1-benzisoxazoles via Conversion of Diethyl α-(o-Nitroaryl)benzylphosphonates

429

Synthesis of 3-phenylnaphthalenic derivatives as new selective MT2 melatoninergic ligands Original Research Article

430

Synthesis of 3-phenylpyrazolo[4,3-b]pyridines via a convenient synthesis of 4-amino-3-arylpyrazoles and SAR of corticotropin-Releasing factor receptor type-1 antagonists

431

Synthesis of 3-Phenylsulfanyl-1,2-dihydronaphthalenes from Methylenecyclopropanes and Benzenethiol

432

Synthesis of 3-pyrroline via domino Heck–aza-Michael reaction

433

Synthesis of 3-pyrroline-2-ones from amino acids and an aryl amine

434

Synthesis of 3-quinolinecarboxylic acid esters from the Baylis–Hillman adducts of 2-halobenzaldehyde N-tosylimines

435

Synthesis of 3-S-alkyl-3-thio-d-glucose derivatives as new non-ionic surfactants and calcium antagonists

436

Synthesis of 3-silyl-2(5H)-furanone by rhodium-catalyzed cyclocarbonylation

437

Synthesis of 3-spiropyrrolidine-3-spirooxindoles from Baylis–Hillman adducts of chromone with azomethine ylides via [3+2] cycloaddition reaction

438

Synthesis of 3-substituted 3H-indol-3-ols by the reaction of 2-isocyanophenyl ketones with Grignard reagents

439

Synthesis of 3-substituted 8,9-didehydroazepino[4,5-b]indolines via ring expansion reaction of pyrroloindolines

440

Synthesis of 3-substituted 8-hydroxy-3,4-dihydroisocoumarins via successive lateral and ortho-lithiations of 4,4-dimethyl-2-(o-tolyl)oxazoline

441

Synthesis of 3-Substituted and 2,3-Disubstituted-4H-1,4-Benzoxazines

442

Synthesis of 3-substituted and 3,4-disubstituted pyrazolin-5-ones

443

Synthesis of 3-Substituted Benzamides and 5-Substituted Isoquinolin-1(2H)-ones and Preliminary Evaluation as Inhibitors of Poly(ADP-ribose)polymerase (PARP) Original Research Article

444

Synthesis of 3-substituted benzo[g]isoquinoline-5,10-diones: a convenient one-pot Sonogashira coupling/iminoannulation procedure

445

Synthesis of 3-substituted carbazole derivative as a host material for deep blue phosphorescent organic light-emitting diodes

446

Synthesis of 3-substituted imidazo[1,5-a]pyridines having 1-(N-picolinamidin-2-yl) group

447

Synthesis of 3-substituted indazoles and benzoisoxazoles via Pd-catalyzed cyclization reactions: application to the synthesis of nigellicine

448

Synthesis of 3-substituted Indoles through Yonemitsu Reaction with Copper Benzene-1,3,5-tricarboxylate acid Catalyst

449

Synthesis of 3-substituted isoindolin-1-ones via a palladium-catalysed 3-component carbonylation/amination/Michael addition process

450

Synthesis of 3-substituted-4-hydroxyquinoline N-oxides from the Baylis–Hillman adducts of o-nitrobenzaldehydes

451

Synthesis of 3-sulfanylpropanols containing three consecutive stereocenters via tandem Michael–aldol reaction of enoylthioamides with acetals as key reaction

452

Synthesis of 3-trialkylsilyl pyrazoles from β-oxo acylsilanes

453

Synthesis of 3-vinyl-2,5-dihydrofuran ring system via enyne metathesis

454

Synthesis of 3Y–ZrO2 nano-powders via a W/O emulsion

455

Synthesis of 3β-(5′-d-ribityl)cholestane, a putative biological precursor for fossil 3-alkylsteranes

456

Synthesis of 3β,6α-dihydroxy-5α-cholan-23-one

457

Synthesis of 3-β-d-ribofuranosyl-1 H-pyrazole-4-carboxamide

458

Synthesis of 3-β-d-ribofuranosylpyrazole-1-carboxamide

459

Synthesis of 4- and 6-substituted nitroindoles

460

Synthesis of 4-(1-oxo-isoindoline) and 4-(5,6-dimethoxy-1-oxo-isoindoline)-substituted phenoxypropanolamines and their β1-, β2-adrenergic receptor binding studies

461

Synthesis of 4-(2-arylvinyl)-8-hydroxyquinolines via anhydrous Heck coupling reaction and the PL properties of their Al complexes

462

Synthesis of 4-(2-hydroxy-1-methyl-5-oxo-1H-imidazol-4(5H)-ylidene)-5-oxo-1-aryl-4,5-dihydro-1H-pyrrole-3-carboxylates, a new triazafulvalene system

463

Synthesis of 4-(2-hydroxyaryl)-3-nitro-4H-chromenes

464

Synthesis of 4-(2-Methylthiazol-4-yl)-Hexahydroquinoline and 1,4-Dihydropyrimidin Derivatives

465

Synthesis of 4-(4,6-di-O-benzyl-2,3-dideoxy-β-d-erythro-hex-2-enopyranosyl)pyrazoles from 3,4,6-tri-O-acetyl-d-glucal

466

Synthesis of 4(5)-phenylimidazole-based analogues of sphingosine-1-phosphate and FTY720: Discovery of potent S1P1 receptor agonists

467

Synthesis of 4-(5-[18F]fluoromethyl-3-phenylisoxazol-4-yl)benzenesulfonamide, a new [18F]fluorinated analogue of valdecoxib, as a potential radiotracer for imaging cyclooxygenase-2 with positron emission tomography

468

Synthesis of 4-(8-benzo[1,2,5]oxadiazol-5-yl-[1,7]naphthyridine-6-yl)-benzoic acid: a potent and selective phosphodiesterase type 4D inhibitor

469

Synthesis of 4-(cyclic dialkylamino)-7-azaindoles by microwave heating of 4-halo-7-azaindoles and cyclic secondary amines

470

Synthesis of 4(S)-(N-Boc-amino)-2(S/R)-(thymin-1-ylmethyl)-pyrrolidine-N-1-acetic acid: a novel cyclic PNA with constrained flexibility

471

Synthesis of 4-(thien-2-yl)-substituted coumarins through Lewis acid catalyzed Michael addition of thiophenes to 3-benzoylcoumarins followed by oxidation

472

Synthesis of 4-(trifluoromethyl) coumarins using nano sulfated-titania as solid acid catalyst under solvent-free conditions

473

Synthesis of 4-(trifluoromethyl)isoquinolines. Influence of trifluoromethyl group on the Pictet–Gams ring closure reaction

474

Synthesis of 4-, 5-, 6-, and 7-azidotryptamines

475

Synthesis of 4-, 8-, 12-arm star-branched polybutadienes with three different chain-end functionalities using a functionalized initiator

476

Synthesis of 4,17-diazasteroid inhibitors of human 5α-reductase Original Research Article

477

Synthesis of 4,4-(arylmethylene)bis(1H-pyrazol-5-ols) via multi-component reactions by using silica-bonded sulfamic acid derivatives

478

Synthesis of 4,4-(arylmethylene)bis(1H-pyrazol-5-ols) via multi-component reactions by using silica-bonded sulfamic acid derivatives

479

Synthesis of 4,4´-(arylmethylene)bis(1H-pyrazol-5-ols) catalyzed by nanosilica supported perchloric acid in water

480

Synthesis of 4,4΄-Diaminotriphenylmethane Derivatives Using H3PW12O40 and HZSM5 Zeolite under Solvent-Free Conditions

481

Synthesis of 4,4-bis(2-hydroperoxyalkyl)pyrazolidine-3,5-diones using manganese(III)-catalyzed autoxidation

482

Synthesis of 4,4-dialkoxy-3-piperidinols. Application to the synthesis of γ-acetate dehydropipecolinonitrile

483

Synthesis of 4,4-dimethyl-3,5-bis(diphenylphosphino)cyclohexanone

484

Synthesis of 4,5,6,7-tetrahydrothieno[3,2-c]pyridines and comparison with their isosteric 1,2,3,4-tetrahydroisoquinolines as inhibitors of phenylethanolamine N-methyltransferase Original Research Article

485

Synthesis of 4,5-diaryl-1,2,3-benzenetricarboxylates by reaction of 4-hydroxycyclopent-2-en-1-one-2-carboxylates with dimethyl acetylenedicarboxylate

486

Synthesis of 4,5-diarylquinazolines: a system with cofacial aromatic rings. Diazines. Part 39

487

Synthesis of 4,5-difluoroimidazole

488

Synthesis of 4,5-disubstituted-3-trihalomethylisothiazoles

489

Synthesis of 4,5-fused tricyclic quinolines via an acid-promoted intramolecular Friedel–Crafts allenylation of aniline derivatives

490

Synthesis of 4,6:2′,3′:4′,6′-tri-O-cyclohexylidene-α,α′-trehalose 2-palmitate: an intermediate for the synthesis of mycobacterial 2,3

491

Synthesis of 4,6-diamino-5-(polyhydroxyalkylamido)pyrimidines: conformation of the sugar chain

492

Synthesis of 4,6-dimethyl-tetrahydro- and hexahydro-dibenzothiophene

493

Synthesis of 4,6-disubstituted pyrimidines via Suzuki and Kumada coupling reaction of 4,6-dichloropyrimidine

494

Synthesis of 4,7-indoloquinones from indole-7-carbaldehydes by Dakin oxidation

495

Synthesis of 4,8-anhydro-d-glycero-d-ido-nonanitol 1,6,7-trisphosphate as a novel IP3 receptor ligand using a stereoselective radical cyclization reaction based on a conformational restriction strategy

496

Synthesis of 4,8-Diarylcinnolines and Quinazolines with Potential Applications in Nonlinear Optics. Diazines. Part 28

497

Synthesis of 4-[N-methyl-4-pyridinio]-phenolate (POMP) and negative solvatochromism of this model molecule in view of nonlinear optical applications

498

Synthesis of 4′,4′-C-diaminomethyl nucleoside derivative as a building block for constructing libraries via amide bond formation

499

Synthesis of 4′-aryl-2′,3′-dideoxynucleoside analogues

500

Synthesis of 4′-benzoyloxycordycepin from adenosine

501

Synthesis of 4′-C, 3′-O bicyclic thymidine analogues using ring closure metathesis

502

Synthesis of 4′-epi-iodo-4′-deoxy-daunorubicin, a potential cancer radiotherapeutic agent

503

Synthesis of 4′-fluoroadenosine as an inhibitor of S-adenosyl-L-homocysteine hydrolase

504

Synthesis of 4′-modified noraristeromycins to clarify the effect of the 4′-hydroxyl groups for inhibitory activity against S-adenosyl-l-homocysteine hydrolase

505

Synthesis of 4′-O-acetyl-maltose and α-d-galactopyranosyl-(1→4)-d-glucopyranose for biochemical studies of amylose biosynthesis Original Research Article

506

Synthesis of 4′-substituted 2,2′:6′,2″-terpyridines via a Mitsunobu reaction

507

Synthesis of 4′-thionucleosides by 1,3-dipolar cycloadditions of the simplest thiocarbonyl ylide with alkenes bearing electron-withdrawing groups

508

Synthesis of 4″-alkoxy avermectin derivatives using rhodium carbenoid-mediated O–H insertion reaction

509

Synthesis of 45S5 Bioglass® via a straightforward organic, nitrate-free sol–gel process

510

Synthesis of 4A zeolites from kaolin for obtaining 5A zeolites through ionic exchange for adsorption of arsenic

511

Synthesis of 4-acylpyrazolone Schiff base ligand grafted silica and selectivity in adsorption of lanthanides from aqueous solutions

512

Synthesis of 4-alkoxy-2-phenylquinoline derivatives as potent antiplatelet agents

513

Synthesis of 4-alkoxy-4-methyl- and 4-alkoxy-4-fluoromethyl-1,3-benzoxazinones

514

Synthesis of 4-alkoxycarbonyl-butenolides by uncatalyzed one-pot cyclization of 1,3-bis(silyloxy)alk-1-enes with oxalyl chloride

515

Synthesis of 4-alkyl-1-benzhydryl-2-(methoxymethyl)azetidin-3-ols by regio- and stereoselective alkylation of 1-benzhydryl-3-(N-alkyl)imino-2-(methoxymethyl)azetidine

516

Synthesis of 4-alkyl-3-bromo-2(5H)-furanones and unsymmetrically disubstituted 3,4-dialkyl-2(5H)-furanones by palladium-catalyzed cross-coupling reactions

517

Synthesis of 4-alkyl-pyrrolidine-3-carboxylic acid stereoisomers

518

Synthesis of 4-allenyl and 4-proparyl-2-azetidinone via Zn-mediated Barbier-type reaction and Pt-catalyzed intramolecular amidation to carbapenem skeletons

519

Synthesis of 4-allylquinazolines from N-(2-cyanoaryl)amides via the In-mediated allylation of nitrile and dehydrative cyclization cascade

520

Synthesis of 4-amino-1,2,3,4-tetrahydropyridine derivatives by intramolecular nucleophilic addition of tertiary enamides to in-situ generated imines

521

Synthesis of 4-amino-3-oxo-tetrahydroazepino[3,4-b]indoles: new conformationally constrained Trp analogs

522

Synthesis of 4-amino-4,5-dideoxy-l-lyxofuranose derivatives and their evaluation as fucosidase inhibitors Original Research Article

523

Synthesis of 4-amino-6-(hetero)arylalkylamino-1,2,4-triazolo[4,3-a]quinoxalin-1-one derivatives as potent A2A adenosine receptor antagonists Original Research Article

524

Synthesis of 4-aminoguaiazulene and its δ-lactam derivatives

525

Synthesis of 4-anilinopiperidine methyl esters, intermediates in the production of carfentanil, sufentanil, and remifentanil

526

Synthesis of 4-arms hydroxy-functionalized PMMA-b-PE through combining free radical polymerization with coordination polymerization

527

Synthesis of 4-aryl-, 2,4-diaryl- and 2,4,7-triarylpyrrolo[2,3-d]pyrimidines by a combination of the Suzuki cross-coupling and N-arylation reactions

528

Synthesis of 4-aryl-2,3-dihydropyrroles via Rh-catalyzed intramolecular hydroamino-methylation reaction

529

Synthesis of 4-aryl-3-methyl-6-oxo-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridine-5-carbonitrile via a one-pot, three-component reaction

530

Synthesis of 4-Aryl-4H-Chromene Derivatives with Boric Acid: Evaluation of Their in vitro Anti-Angiogenesis Effects and Possible Mechanism of Action

531

Synthesis of 4-aryl-5,5-dimethyl-5H-1,2,3-triazoles and 4-aryl-3-cyano-5,5-dimethyl Δ1-pyrazolines by cycloaddition of 2-diazopropane with iminoethers and propenenitriles

532

Synthesis of 4-aryl-5-hydroxy- and 5-aryl-4-hydroxypyridazin-3(2H)-ones and their use in the preparation of 4,5-diarylpyridazin-3(2H)-ones and hitherto unknown isochromeno[3,4-d]pyridazinediones

533

Synthesis of 4-aryl-6-indolylpyridine-3-carbonitriles and evaluation of their antiproliferative activity

534

Synthesis of 4-Arylaminoquinazolines and 2-Aryl-4-arylaminoquinazolines from 2-Aminobenzonitrile, Anilines and Formic Acid or Benzaldehydes

535

Synthesis of 4-aryl-azetidinones via intramolecular alkylation of nucleophilic arenes using acyliminium cations

536

Synthesis of 4-arylidenecyclohexane-1,3-diones from the Baylis–Hillman acetates

537

Synthesis of 4-aza analog of ramelteon: a novel tricyclic 1,6,7,8-tetrahydro-2H-cyclopenta[d]furo[2,3-b]pyridine derivative as melatonin receptor ligand

538

Synthesis of 4-aza tricyclo [6.2.2.01,6]dodecenone and photoreactions: a stereoselective, entry to aza-polycyclic systems related to magellanine and congeners

539

Synthesis of 4-azacyclopent-2-enones and 5,5-dialkyl-4-azacyclopent-2-enones

540

Synthesis of 4-azepanones and heteroaromatic-fused azepines

541

Synthesis of 4-aziridino[C60]fullerene-1,8-naphthalimide (C60-NI dyads) and their photophysical properties

542

Synthesis of 4-Azo-3,5-Substituted-1,2,4-Triazole Polymers and Study of their Applications

543

Synthesis of 4b,5,10a,11-tetrahydroindeno[1,2-b]quinolin-10-ones from Baylis–Hillman adducts

544

Synthesis of 4-benzyl-3-phenylbutenolide natural products

545

Synthesis of 4-butyl-1-substituted-4H-[1,2,4]triazolo[4,3-a]quinazolin-5-ones as new class of H1-antihistaminic agents

546

Synthesis of 4-carboxy-4-pyridylpiperidines through palladium-catalyzed α-arylation of esters

547

Synthesis of 4-cyano and 4-nitrophenyl 1,6-dithio-d-manno-, l-ido- and d-glucoseptanosides possessing antithrombotic activity Original Research Article

548

Synthesis of 4-cyano- and 4-nitrophenyl 2,5-anhydro-1,6-dithio-α-d-gluco- and -α-l-guloseptanosides carrying different substituents at C-3 and C-4 Original Research Article

549

Synthesis of 4-cyanophenyl 1,5-dithio-β-d-glucopyranoside and its 6-deoxy, as well as 6-deoxy-5-ene derivatives as oral antithrombotic agents

550

Synthesis of 4-cyanophenyl 2-azido-2-deoxy- and 3-azido-3-deoxy-1,5-dithio-β-d-xylopyranosides

551

Synthesis of 4-cyanophenyl 2-deoxy-1,5-dithio-β-d-threo-pentopyranoside

552

Synthesis of 4-cyanophenyl 4-azido-4-deoxy-1,5-dithio-β-d-xylopyranoside

553

Synthesis of 4-cyanophenyl and 4-nitrophenyl 1,5-dithio-d-ribopyranosides as well as their 2-deoxy and 2,3-dideoxy derivatives possessing antithrombotic activity

554

Synthesis of 4-cyanophenyl and 4-nitrophenyl 1,5-dithio-l- and -d-arabinopyranosides possessing antithrombotic activity

555

Synthesis of 4-cyanophenyl and 4-nitrophenyl 2-azido-2-deoxy-1,5-dithio-β-d-arabino- and -β-d-lyxopyranosides possessing antithrombotic activity

556

Synthesis of 4-demethoxyadriamycinone utilizing ruthenium-catalyzed oxidation of allyl acetates

557

Synthesis of 4-deoxy analogues of 2-acetamido-2-deoxy-d-glucose and 2-acetamido-2-deoxy-d-xylose and their effects on glycoconjugate biosynthesis Original Research Article

558

Synthesis of 4-deoxy-4-fluoro analogues of 2-acetamido-2-deoxy-d-glucose and 2-acetamido-2-deoxy-d-galactose and their effects on cellular glycosaminoglycan biosynthesis Original Research Article

559

Synthesis of 4-dialkylaminopyridine derivatives through ring-rearrangement of 3-nitro-2H-pyran-2-one acetamidines

560

Synthesis of 4-Diphosphocytidyl-2-C-Methyl-D-Erythritol 2-Phosphate and Kinetic Studies of Mycobacterium tuberculosis IspF

561

Synthesis of 4-epi-2-deoxy-2-Heq-N-acetylneuraminic acid and 2,4-dideoxy-2-Heq N-acetylneuraminic acid

562

Synthesis of 4-fluoroalkyl-substituted pyridazines from fluorinated diazodiketones

563

Synthesis of 4-functionalized aryl-3,5-diacyl-1,4-dihydropyridines

564

Synthesis of 4-functionalized terdendate pyridine-based ligands

565

Synthesis of 4H-[1,3]dithiolo[4,5-b]pyrroles through the reaction of benzoyl isothiocyanate and dialkyl acetylenedicarboxylates in the presence of Ph3P

566

Synthesis of 4-halophosphaisocoumarins via halocyclization of 2-(1-alkynyl)phenylphosphonates

567

Synthesis of 4-haloserotonin derivatives and synthesis of the toad alkaloid dehydrobufotenine

568

Synthesis of 4H-benzo[e]-1,2-selanazin-4-one derivatives: a new heterocyclic ring system

569

Synthesis of 4H-pyrano[2,3-d]pyrimidine derivatives under solvent-free conditions

570

Synthesis of 4H-pyrans catalyzed by thermol-regulated PEG1000-based ionic liquid/EM

571

Synthesis of 4-hydroxy- and 2,4-dihydroxy-homophthalates by [4+2] cycloaddition of 1,3-bis(silyloxy)-1,3-butadienes with dimethyl allene-1,3-dicarboxylate

572

Synthesis of 4-hydroxy-1-methylindole and benzo[b]thiophen-4-ol based unnatural flavonoids as new class of antimicrobial agents Original Research Article

573

Synthesis of 4-hydroxy-3-[(E)-2-(6-substituted-9H-purin-9-yl)vinyl]coumarins as lipoxygenase inhibitors

574

Synthesis of 4-hydroxy-7-dimethylamino-3-pyrazolinylcoumarins and their polarity-sensitive properties

575

Synthesis of 4-hydroxyderricin and related derivatives

576

Synthesis of 4-hydroxymethyl-2,4-methanoproline

577

Synthesis of 4-hydroxysphinganine and characterization of sphinganine hydroxylase activity in corn

578

Synthesis of 4-Methoxy-1, 3-Benzenediolylhydrazones and Evaluation of Their Anti-Platelet Aggregation Activity

579

Synthesis of 4-methoxy-1H-phenalen-1-one: a subunit related to natural phenalenone-type compounds

580

Synthesis of 4-methoxy-3,5-dinitrobenzaldehyde: a correction to supposed tele nucleophilic aromatic substitution

581

Synthesis of 4-methylcoumarin-7-yl β-d-galactofuranoside, a fluorogenic substrate for galactofuranosidase

582

Synthesis of 4-methyl-thio-phenyl-propylamine and the evaluation of its interaction with different amine oxidases Original Research Article

583

Synthesis of 4-methylumbelliferyl-β-d-glucan oligosaccharides as specific chromophoric substrates of (1 → 3),(1 → 4)-β-d-glucan 4-glucanohydrolases

584

Synthesis of 4-monofluoromethylenyl- and cis-4-monofluoromethyl-l-pyroglutamic acids via a novel dehydrofluorination

585

Synthesis of 4-N-alkyl and ribose-modified AICAR analogues on solid support

586

Synthesis of 4-nitromethylene-1,4-dihydropyrimidine derivatives as pyrimidine nucleoside analogues

587

Synthesis of 4-Nitrophenyl Sulfones and Application in the Modified Julia Olefination

588

Synthesis of 4-nitrophenyl β-d-fucofuranoside and β-d-fucofuranosyl-(1→3)-d-mannopyranose: modified substrates for studies on catalytic requirements of β-d-galactofuranosidase

589

Synthesis of 4-O- and 6-O-(2′-iodoethyl)-d-glucose

590

Synthesis of 4-O-[3-(aryl)prop-2-ynyl]-Neu5Ac2en and its 4-epi-analogs modified at C-4 by Sonogashira coupling reaction

591

Synthesis of 4-O-d-Mannopyranosyl-α-d-glucopyranosides by Intramolecular Glycosylation of 6-O-Tethered Mannosyl Donors

592

Synthesis of 4-O-glycosylated 1,5-anhydro-d-fructose and of 1,5-anhydro-d-tagatose from a common intermediate 2,3-O-isopropylidene-d-fructose

593

Synthesis of 4-O-glycosylated 1-deoxynojirimycin derivatives as disaccharide mimics-based inhibitors of human β-glucocerebrosidase

594

Synthesis of 4-oxepanones by the Lewis acid-promoted ring-expansion reaction of cyclopropapyranones

595

Synthesis of 4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-carboxylic acid ethyl ester and its isomer 1-oxo-2,9-dihydro-1H-β-carboline-4-carboxylic acid ethyl ester

596

Synthesis of 4-oxo-4,7-dihydrofuro[2,3-b]pyridine-5-carboxamides with broad-spectrum human herpesvirus polymerase inhibition

597

Synthesis of 4-pentenoic and 5-hexenoic acids on polystyrene resin and their use as cleavable linkers

598

Synthesis of 4-phenoxybenzamide adenine dinucleotide as NAD analogue with inhibitory activity against enoyl-ACP reductase (InhA) of Mycobacterium tuberculosis

599

Synthesis of 4-Phenyl-4,5-dihydropyranopyrazolone Derivatives with Activated Potassium Carbonate: Evaluation of Anticancer Activity on Cancer Cell Lines and Apoptosis Mechanism

600

Synthesis of 4-phenylpyrrolidin-2-one via dynamic kinetic resolution catalyzed by ω-transaminases

601

Synthesis of 4-phosphono-β-lactams via phosphite addition to acyliminium salts

602

Synthesis of 4-Pyrazolylmethylidene-2-Oxazoline and -2-Imidazoline Derivatives

603

Synthesis of 4-pyrido-6-aryl-2-substituted amino pyrimidines as a new class of antimalarial agents Original Research Article

604

Synthesis of 4-substituted 3-(indol-3-yl)maleimides and azepines with annelated indole and maleimide nuclei

605

Synthesis of 4-substituted 4-arylpiperidines

606

Synthesis of 4-substituted and 3,4-disubstituted indazole derivatives by palladium-mediated cross-coupling reactions

607

Synthesis of 4-substituted azepino[3,4-b]indole-1,5-diones

608

Synthesis of 4-substituted homoallylic alcohols via a one-pot tandem Lewis-acid catalyzed crotylboration-[3,3]-sigmatropic rearrangement

609

Synthesis of 4-substituted phenyl 2,5-anhydro-1,6-dithio-α-d-gluco- and -α-l-guloseptanosides possessing antithrombotic activity Original Research Article

610

Synthesis of 4-substituted phenyl 3,6-anhydro-1,3-dithio-d-glucofuranosides and -pyranosides as well as 2,6-anhydro-1,2-dithio-α-d-altrofuranosides possessing antithrombotic activity Original Research Article

611

Synthesis of 4-Substituted Phosphacoumarins via Cross-Coupling of 4-Tosylphosphacoumarins with Organozinc Reagents

612

Synthesis of 4-substituted pyrano[4,3-b]pyran-2,5-diones in an ionic liquid

613

Synthesis of 4-substituted tetrahydropyridines by cross-coupling of enol phosphates

614

Synthesis of 4-substituted-2-acetamido-2,4-dideoxy-mannopyranoses using 1,6-anhydro sugar chemistry

615

Synthesis of 4-sulfonatooxy-2,2,6,6-tetramethylpiperidine-1-yloxyl derivatives for investigation of ionic liquids

616

Synthesis of 4-thiaharmalan analogue 4-aryl-1,3-thiazino[5,6-b]indole derivatives by prevention of rearrangements to position two of the indole moiety

617

Synthesis of 4-thiofuranoid 1,2-glycals and their application to stereoselective synthesis of 4′-thionucleosides

618

Synthesis of 4-thiophen-2′-yl-1,4-dihydropyridines as potentiators of the CFTR chloride channel Original Research Article

619

Synthesis of 4-Thiothymine Based Photolabels as New Tools for Nucleic Acids Structural Studies in Solution: Formation of Long-Range Photo-Cross-Links within a Hammerhead Ribozyme Domain

620

Synthesis of 4-trifluoromethylpyrido[1,2-a]pyrimidin-2-ones utilizing activated alkynoates

621

Synthesis of 4-trifluoromethylsteroids: A novel class of steroid 5α-reductase inhibitors

622

Synthesis of 4-trimethylammonio-2,2,6,6-tetramethylpiperidine-1-yloxyl with various anions for investigation of ionic liquids

623

Synthesis of 4-unsubstituted 2H-1,2,3-benzothiadiazine 1,1-dioxides via ortho lithiation of protected benzaldehyde derivatives

624

Synthesis of 4-unsubstituted dihydropyrimidines having acyl and alkoxycarbonyl groups at 5- and 6-positions by cyclization–elimination reactions using 1,3-diaza-1,3-butadienes

625

Synthesis of 4-unsubstituted dihydropyrimidines. Nucleophilic substitution at position-2 of dihydropyrimidines

626

Synthesis of 5- and 6-(6-Chloro-3-pyridyl)-2-azabicyclo[2.2.0]hexanes. Epibatidine Analogs

627

Synthesis of 5-(1-H or 1-alkyl-5-oxopyrrolidin-3-yl)-8-hydroxy-[1,6]-naphthyridine-7-carboxamide inhibitors of HIV-1 integrase

628

Synthesis of 5(20)deoxydocetaxel, a new active docetaxel analogue

629

Synthesis of 5-(2-amino-2-deoxy-β- -glucopyranosyloxymethyl)-2′-deoxyuridine and its incorporation into oligothymidylates

630

Synthesis of 5-(2-aryl-2-haloethyl)salicylates by the first domino ‘[3+3] cyclization/ring-cleavage’ reactions of 1,3-bis(silyloxy)-1,3-butadienes with 3-acetyl-5-aryl-4,5-dihydrofurans

631

Synthesis of 5-(3,4-dichlorophenyl)-4-[(methyloxy)methyl]-2-azabicyclo[3.2.1]octane derivatives as constrained aryl-piperidines with activity as triple re-uptake inhibitors

632

Synthesis of 5-(3-indolyl)oxazole natural products. Structure revision of Almazole D

633

Synthesis of 5(6)-dihydro-OSW-1 by using the intact skeleton of tigogenin

634

Synthesis of 5-(7′-indolyl)oxazoles and 2,5-di-(7′-indolyl)oxazoles

635

Synthesis of 5-(7-hydroxyhept-3-enyl)-1,2-dithiolan-3-one 1-oxide, a core functionality of antibiotic leinamycin

636

Synthesis of 5-(mercaptomethyl)-3(E)-undecene-1,11-dioic acid, a non-peptide glutathione analog

637

Synthesis of 5-(perfluoroalkylmethyl)-1,3-dioxolan-4-ones

638

Synthesis of 5-(phenylsulfanyl)-1,4-dihydropyrazine-2,3-diones via an unexpected microwave-assisted cascade reaction

639

Synthesis of 5-(sulfamoylmethyl)indoles

640

Synthesis of 5-(trifluoromethyl)-5H-chromeno[3,4-b]pyridines from 3-nitro-2-(trifluoromethyl)-2H-chromenes and aminoenones derived from acetylacetone and cyclic amines

641

Synthesis of 5-(trifluoromethyl)cyclohexane-1,3-dione and 3-amino-5-(trifluoromethyl)cyclohex-2-en-1-one: new trifluoromethyl building block

642

Synthesis of 5-(ω-sulfhydrylalkyl)salicylaldehydes as precursors for the preparation of alkanethiol-modified metal salens

643

Synthesis of 5,10,15,20-tetrakis(2-amino-5-methoxyphenyl)-porphyrin: a versatile building block for porphyrin face selection

644

Synthesis of 5,10-diphenylporphyrin

645

Synthesis of 5,15-diarylporphyrins via orthoesters condensation with aryldipyrromethanes

646

Synthesis of 5,5,6,6,21,21,22,22-octamethyl-5,6,21,22-tetragerma[10.10]paracyclophane

647

Synthesis of 5,5′-bis-benzofurans and 5-arylbenzofurans

648

Synthesis of 5,5′-diarylated 2,2′-bithiophenes via palladium-catalyzed arylation reactions

649

Synthesis of 5,6-bis(alkyn-1-yl)pyrimidines and related nucleosides

650

Synthesis of 5,6-Dihydro-11H-benzo[5,6]-cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidine-N-cyanoguanidine Derivatives as Inhibitors of Ras Farnesyl Protein Transferase

651

Synthesis of 5,6-dihydro-2H-thiins and 2,3-dihydro-1,4-oxathiins based on 1-benzylsulfonyl-1,1-dihydropolyfluoroalkan-2-ones

652

Synthesis of 5,6-dihydro-4H-1,3-thiazine containing peptide mimics from N-(3-hydroxypropyl)thioamides and epimerization studies

653

Synthesis of 5,6-dihydro-4-hydroxy-2-pyrones via formal cycloaddition reactions

654

Synthesis of 5,6-dihydrobenz[c]acridines: a comparative study

655

Synthesis of 5,6-dihydrophenanthridines via N,O-acetal TMS ethers

656

Synthesis of 5,7,12,14-Tetraarylpentacenes from Pentacene-5,7,12,14-tetrone and Characterisation of the Tetrol Intermediates

657

Synthesis of 5,8-dimethoxy-3-hydroxy-4-quinolone, a reported inhibitor of HIV RT, and evidence the original proposed structure was incorrect

658

Synthesis of 5′,9-anhydro-3-(β-d-ribofuranosyl)xanthine, and 3,5′-anhydro-xanthosine as potential anti-hepatitis C virus agents

659

Synthesis of 5′-C-methyl-1′,3′-dioxolan-4′-yl nucleosides

660

Synthesis of 5′-functionalized adenosine: suppression of cyclonucleoside formation

661

Synthesis of 5′-functionalized nucleosides: S-Adenosylhomocysteine analogues with the carbon-5′ and sulfur atoms replaced by a vinyl or halovinyl unit Original Research Article

662

Synthesis of 5′-seleno-xylofuranosides

663

Synthesis of 5′-substituted fluoro-neplanocin A analogues: importance of a hydrogen bonding donor at 5′-position for the inhibitory activity of S-adenosylhomocysteine hydrolase

664

Synthesis of 5″-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca2+-mobilizing agent: The first antagonists modified at the N1-ribose moiety

665

Synthesis of 5a-carba-hexopyranoses and hexopyranosylamines, as well as 5a,5a′-dicarbadisaccharides, from 3,8-dioxatricyclo[4.2.1.02,4]nonan-9-ol: glycosidase inhibitory activity of N-substituted 5a-carba-β-gluco- and β-galactopyranosylamines, and derivat

666

Synthesis of 5-Acetoxy-2(5H)-Furanones through Manganese(III)-Promoted Functionalization of Arylacetylenes

667

Synthesis of 5-acetyl-2-aminopyrrole C-deoxyribonucleoside

668

Synthesis of 5-alkoxymethyl- and 5-aminomethyl-substituted 8-hydroxyquinoline derivatives and their luminescent Al(III) complexes for OLED applications

669

Synthesis of 5-alkyl(or aryl)pyrrolo[1,2-a]quinoxalin-4(5H)-ones by denitrocyclisation of N-alkyl(or aryl)-1-(2-nitrophenyl)-1H-pyrrole-2-carboxamides. Evidence of a Smiles rearrangement

670

Synthesis of 5-alkyl-3,4-difluorofuran-2(5H)-ones by lactonisation. Effects of substituents on cyclisation ability of fluorinated 4-hydroxyalkanoates. DFT calculations of the cyclisation energies

671

Synthesis of 5-alkyl-4-amino-2-(trifluoromethyl)pyridines and their transformation into trifluoromethylated 1H-pyrazolo[4,3-c]pyridines

672

Synthesis of 5-alkylidene-2,5-dihydropyrrol-2-ones and their ring-transformation into 5,6-dihydrobenzo[h]chromones, 5,6,7,8-tetrahydrochromones and pyran-4-ones

673

Synthesis of 5-alkylidene-2,5-dihydropyrrol-2-ones based on cyclizations of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with oxalyl chloride

674

Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles

675

Synthesis of 5-alkynylated uracil–morpholino monomers using Sonogashira coupling

676

Synthesis of 5-amino-1-aryl-4-cyanoimidazoles from formamidines under solvent-free condition

677

Synthesis of 5-amino-2-aminoalkyl-1,3-oxazol-4-ylphosphonic acid derivatives and their use in the preparation of phosphorylated peptidomimetics

678

Synthesis of 5-amino-2-selenoxo-1,3-imidazole-4-carboselenoamides by the reaction of isoselenocyanates with aminoacetonitriles

679

Synthesis of 5-aminoisoxazolines from N-allyl compounds and nitrile oxides via tandem isomerization-1,3-dipolar cycloaddition

680

Synthesis of 5-aminothiazoles as building blocks for library synthesis

681

Synthesis of 5-aryl-3H-[1,3,4]oxadiazol-2-ones from N′-(chloro-aryl-methylene)-tert-butylcarbazates using basic alumina as an efficient and recyclable surface under solvent-free condition

682

Synthesis of 5-aryl-5′-formyl-2,2′-bithiophenes as new precursors for nonlinear optical (NLO) materials

683

Synthesis of 5-arylamino-1-arylpyrazoles from 5-aminopyrazoles with arylhalides via CuI catalyzed Ullman coupling reaction

684

Synthesis of 5-arylhistidines via a Suzuki–Miyaura cross-coupling

685

Synthesis of 5-arylidene-2-amino-4-azolones and evaluation of their anticancer activity Original Research Article

686

Synthesis of 5-arylidene-2-aryl-3-(2-chlorophenothiazinoacetamidyl)l,3-thiazolidin-4-ones as antifungal and anticonvulsant agents

687

Synthesis of 5-arylmethylene-pyrimidine-2,4,6-trione and 2-arylidenemalononitriles derivatives using a new Brønsted acid nano magnetic catalyst

688

Synthesis of 5-arylpyrrolo[2,1-c][1,4]benzodiazepines under mild cyclodehydration conditions

689

Synthesis of 5-arylthiazoles. Comparative study between Suzuki cross-coupling reaction and direct arylation

690

Synthesis of 5-aryltriazole ribonucleosides via Suzuki coupling and promoted by microwave irradiation

691

Synthesis of 5-aza-analogues of angucyclines: manipulation of the 2-deoxy-C-glycoside subunit

692

Synthesis of 5-benzoylacenaphthene in the presence of Lewis acidic ionic liquids

693

Synthesis of 5-benzyloxy-1,4-dihydro-6-methyl-4-oxopyridine-3-carbaldehyde by aerobic oxidation of the 5-dimethylaminomethyl analogue: optimisation of the reaction conditions

694

Synthesis of 5-bromo-6-methyl imidazopyrazine, 5-bromo and 5-chloro-6-methyl imidazopyridine using electron density surface maps to guide synthetic strategy

695

Synthesis of 5-chloro-N-aryl-1H-indole-2-carboxamide derivatives as inhibitors of human liver glycogen phosphorylase a Original Research Article

696

Synthesis of 5-deazaflavin derivatives and their activation of p53 in cells Original Research Article

697

Synthesis of 5-deazathiogirollines: analogs of a natural antitumor agent

698

Synthesis of 5-deoxy-5-epifluoro derivatives of arbekacin, amikacin, and 1-N-[(S)-4-amino-2-hydroxybutanoyl]tobramycin (study on structure — toxicity relationships)

699

Synthesis of 5-deoxy-5-phospho-d-ribonohydroxamic acid: a new competitive and selective inhibitor of type B ribose-5-phosphate isomerase from Mycobacterium tuberculosis

700

Synthesis of 5-deoxypterocarpens, pterocarpens, and coumestans by intramolecular Heck reaction

701

Synthesis of 5-deoxy-β-d-galactofuranosides as tools for the characterization of β-d-galactofuranosidases Original Research Article

702

Synthesis of 5-endo-, 5-exo-, 6-endo- and 6-exo-hydroxylated analogues of epibatidine

703

Synthesis of 5-epiaragusterol A

704

Synthesis of 5-ethoxymethylfurfural from 5-hydroxymethylfurfural and fructose in ethanol catalyzed by MCM-41 supported phosphotungstic acid

705

Synthesis of 5-Fluorouracil nanoparticles via supercritical gas antisolvent process

706

Synthesis of 5-fluorouridine 5′-diphosphate galactose from 5-fluorouridine by chemical phosphorylation and microbial uridylyl transfer

707

Synthesis of 5-fluorovinyl derivatives of pyrimidines via Suzuki–Miyaura coupling and their 1,3-dipolar cycloaddition reactions with nitrones

708

Synthesis of 5-haloethynyl- and 5-(1,2-dihalo)vinyluracil nucleosides: Antiviral activity and cellular toxicity Original Research Article

709

Synthesis of 5-halogenated 1,2,3-triazoles under stoichiometric Cu(I)-mediated azide–alkyne cycloaddition (CuAAC or ‘Click Chemistry’) Original Research Article

710

Synthesis of 5-heteroarylazulenes: first selective electrophilic substitution at the 5-position of azulene

711

Synthesis of 5H-pyridazino[4,5-b]indoles and their benzofurane analogues utilizing an intramolecular Heck-type reaction

712

Synthesis of 5-HT3 receptor antagonists, [11C]Y-25130 and [11C]YM060

713

Synthesis of 5-Hydroxy- and 5-Amino-1-tosyl-5-phenyl-3-(2-arylvinyl)4,5-dihydropyrazoles

714

Synthesis of 5-hydroxy-2-(β-d-ribofuranosyl)pyran-4-one from a pyranulose glycoside

715

Synthesis of 5-hydroxyquinolines

716

Synthesis of 5-membered heterocycles using benzoylacetonitriles as synthon

717

Synthesis of 5-methoxylated 3-pyrrolin-2-ones via the rearrangement of chlorinated pyrrolidin-2-ones

718

Synthesis of 5-methylfuro[3,2-c]quinolin-4(5H)-one via palladium-catalysed cyclisation of N-(2-iodophenyl)-N-methyl-3-furamide

719

Synthesis of 5-nitro- and 5-aminobenzimidazolone-2

720

Synthesis of 5-O-methylembelin

721

Synthesis of 5-substituted 1H-tetrazoles catalyzed by ceric ammonium nitrate supported HY-zeolite

722

Synthesis of 5-substituted 1H-tetrazoles catalyzed by ytterbium triflate hydrate

723

Synthesis of 5-substituted 2-(4- or 3-methoxyphenyl)-4(1H)-quinolones

724

Synthesis of 5-substituted 2,3-dihydrobenzofurans in a one-pot oxidation/cyclization reaction

725

Synthesis of 5-substituted 3-mercapto-1,2,4-triazoles via Suzuki–Miyaura reaction

726

Synthesis of 5-substituted analogues of huperzine A

727

Synthesis of 5-substituted derivatives of isophthalic acid as non-polymeric amphiphilic coating for metal oxide nanoparticles

728

Synthesis of 5-substituted indole derivatives. Part 3: A facile synthesis of 5-chloromethyl-1H-indole-2-carboxylates: replacement of sulfonic acid functionality by chlorine

729

Synthesis of 5-substituted pipecolic acid derivatives as new conformationally constrained ornithine and arginine analogues

730

Synthesis of 5-substituted quinazolinone derivatives and their inhibitory activity in vitro

731

Synthesis of 5-Substituted-1,3,4-Oxadiazole-2(3H)-Thiones Under Microwave Irradiation

732

Synthesis of 5-substituted-3,4-dihydroxycyanopyrrolidines. An easy access to polyhydroxyprolines

733

Synthesis of 5-thio-l-altrose

734

Synthesis of 5-Thiomannose-containing oligomannoside mimics: Binding abilities to concanavalin A

735

Synthesis of 5-thioxo-6H-imidazo[1,2-c]quinazolines and related compounds based on cyclocondensations of 2-isothiocyanatobenzonitrile (ITCB) with α-aminoketones

736

Synthesis of 5-trichloromethyl-Δ4-1,2,4-oxadiazolines and their rearrangement into formamidine derivatives

737

Synthesis of 6- and 7-propargyloxy derivatives of 4-(3-fluoroanilino)-quinazoline

738

Synthesis of 6- or 4-functionalized indoles via a reductive cyclization approach and evaluation as aromatase inhibitors

739

Synthesis of 6-(2-thienyl)purine nucleoside derivatives that form unnatural base pairs with pyridin-2-one nucleosides

740

Synthesis of 6-(perfluoroalkyl)salicylates by [3+3] cyclization of 1,3-bis(silyl enol ethers) with 3-ethoxy-1-(perfluoroalkyl)prop-2-en-1-ones

741

Synthesis of 6-(Phenanthrene-3-yl)-2,3-dihydro-1,2,4,-triazine-3-thione as a New Reagent for the Non-Extractive Spectrophotometric Determination of Cu(II)

742

Synthesis of 6(α,β)-aminocholestanols as ergosterol biosynthesis inhibitors

743

Synthesis of 6-, 7- and 8-membered cyclosiloxanes having multifunctional groups

744

Synthesis of 6-, 7-, and 8-membered lactones via the nickel-catalysed electrochemical arylation of electron-deficient olefins

745

Synthesis of 6,6-bisbenzannulated spiroketals related to the rubromycins using a double intramolecular hetero-Michael addition (DIHMA)

746

Synthesis of 6,6-Difluorocyclopropa[b]furo[2,3-c]pyrrole and 7-Fluoro furo[3,2-c]pyridine Derivatives via 1,5-Electrocyclization of CarbeneDerived Azomethine Ylides

747

Synthesis of 6,7,8,9-tetrahydropyrido[2,3-b]indolizine and 3,4-dihydro-2H-pyrido[2′,3′:4,5]pyrrolo[2,1-b][1,3]oxazine derivatives as new melatonin receptor ligands

748

Synthesis of 6,7-diaza-19-norvitamin D compounds

749

Synthesis of 6,7-dichloropyrido[1,2-a]benzimidazole-8,9-dione and its analogues and their reactions with nucleophiles

750

Synthesis of 6,7-dideoxy-7-isothiocyanatoheptoses: stable fully unprotected monosaccharide isothiocyanates

751

Synthesis of 6,7-dihydro-5H-dibenzo[c,e]azepines and biaryls by palladium-catalyzed Ullmann reaction

752

Synthesis of 6,7-disubstituted-5H-pyrrolo[2,3-b]pyrazines via palladium-catalyzed heteroannulation

753

Synthesis of 6,7-ethylenedioxyquinoxalines and pyrido[2,3-b]pyrazines as intermediates in the preparation of antineoplastic agents

754

Synthesis of 6,8-substituted-5,7-difluoro-3,4-dihydro-1H-quinoxalin-2-ones via reductive cyclisation of 2,4,6-substituted-3,5-difluoronitrobenzenes

755

Synthesis of 6′-acylamido-6′-deoxy-α-d-galactoglycerolipids Original Research Article

756

Synthesis of 6′-deoxy-6′-fluorosucrose Original Research Article

757

Synthesis of 6′-GM2, a regioisomer of ganglioside GM2, for studying the mechanism of action of GM2 activator

758

Synthesis of 60- and 72 kDa heat shock proteins in early porcine embryogenesis

759

Synthesis of 61-bis(1-adamantylcarbamoyl)-1,2-methano[60]fullerene and its antagonistic effect on haloperidol-induced catalepsy in mice

760

Synthesis of 6-acyl-5,8-quinolinediols by photo-Friedel–Crafts acylation using sunlight

761

Synthesis of 6-Acylmethylphenanthridine Enaminones

762

Synthesis of 6a-hydroxypterocarpans via intramolecular benzoin condensation

763

Synthesis of 6-alkylidene-2,3-benzo-1,4-diaza-7-oxabicyclo[4.3.0]non-2-enes by cyclization of 1,3-bis(silyl enol ethers) with quinoxalines

764

Synthesis of 6-amino-1,6-anhydro-6-deoxysugar derivatives

765

Synthesis of 6-Amino-1H-Indole-4,7- Quinones

766

Synthesis of 6-amino-6-deoxyhyaluronan as an intermediate for conjugation with carboxylate-containing compounds: application to hyaluronan–camptothecin conjugates Original Research Article

767

Synthesis of 6-aryl- and 5-aroylcomanic acids from 5-aroyl-2-carbethoxy-4-pyrones via a deformylative rearrangement and ring-opening/ring-closure sequence

768

Synthesis of 6-aryl-2,4-diamino-pyrimidines and triazines using palladium catalysed Suzuki cross-coupling reactions

769

Synthesis of 6-aryl-2′-deoxyuridine nucleosides via a Liebeskind cross-coupling methodology

770

Synthesis of 6-aryluridines via Suzuki–Miyaura cross-coupling reaction at room temperature under aerobic ligand-free conditions in neat water

771

Synthesis of 6-Aziridineyl and 6-Triazol-yl of D- Glucitol Derivatives

772

Synthesis of 6-bromo-2-arylindoles using 2-iodobenzoic acid as precursor

773

Synthesis of 6-carboxylated phenanthridines by oxidative alkoxycarbonylation–cyclization of 2-isocyanobiphenyls with carbazates

774

Synthesis of 6-chloroisoquinoline-5,8-diones and pyrido[3,4-b]phenazine-5,12-diones and evaluation of their cytotoxicity and DNA topoisomerase II inhibitory activity Original Research Article

775

Synthesis of 6-cyano and 6-unsubstituted 2-aryl-8-oxopurine from a common 2-oxoimidazole precursor

776

Synthesis of 6-deoxy-5-thio-d-glucose

777

Synthesis of 6-deoxy-6-chloro and 6-deoxy-6-bromo derivatives of scleroglucan as intermediates for conjugation with methotrexate and other carboxylate containing compounds

778

Synthesis of 6-deoxy-6-chloro and 6-deoxy-6-bromo derivatives of scleroglucan as intermediates for conjugation with methotrexate and other carboxylate containing compounds

779

Synthesis of 6-deoxy-6-halolaminarans and conversion of 6-chloro-6-deoxylaminaran into the 6-amino-6-deoxy derivative

780

Synthesis of 6-deoxy-l-idose and l-acovenose from 1,2:5,6-di-O-isopropylidene-α-d-glucofuranose Original Research Article

781

Synthesis of 6-deoxy-N-Cbz-d,l-iminoglycal-derived vinyl epoxides and examination of their regio- and stereoselectivity in nucleophilic addition reactions

782

Synthesis of 6-ethynylpurine derivatives

783

Synthesis of 6-formyl-pyridine-2-carboxylate derivatives and their telomerase inhibitory activities

784

Synthesis of 6-formylsalicylates based on regioselective [3+3] cyclocondensations of 1,3-bis(silyloxy)-1,3-butadienes with 1,1-dichloro-4-ethoxy-3-buten-2-ones

785

Synthesis of 6H-benzo[c]chromen-6-ones by cyclocondensation of 1,3-dicarbonyl compounds with 4-chloro-3-formylcoumarin

786

Synthesis of 6H-isoindolo[2,1-a]indol-6-ones through a sequential copper-catalyzed C-N coupling and palladium-catalyzed C–H activation reaction

787

Synthesis of 6H-naphtho[2,3-c]chromene-7,12-diones via palladium-catalyzed intramolecular cyclization of 2-bromo-3-aryloxymethyl-1,4-naphthoquinones

788

Synthesis of 6-hydroxy-2-naphthoic acid from 2,6-diisopropylnaphthalene using NHPI as a key catalyst

789

Synthesis of 6-hydroxymethyl-5,6-dihydro-4H-1,2-oxazines by one-pot-cyclization of dilithiated oximes with epibromohydrin

790

Synthesis of 6I-amino-6I-deoxy-2I–VII,3I–VII-tetradeca-O-methyl-cyclomaltoheptaose

791

Synthesis of 6-imino-5-tetrahydro-1H-2-pyrrolylidenhexahydro-2,4-pyrimidinediones as intermediates for the synthesis of C-azanucleosides

792

Synthesis of 6-methoxy-4H-1-benzopyran-7-ol, a character donating component of the fragrance of Wisteria sinensis

793

Synthesis of 6-methyl-6H-indolo[3,2-c]isoquinoline and 6-methyl-6H-indolo[2,3-c]isoquinoline: two new unnatural isoquinoline isomers of the cryptolepine series

794

Synthesis of 6-N-(benzothiazol-2-yl)deoxyadenosine and its exciton-coupled circular dichroism Original Research Article

795

Synthesis of 6-O-acetyl-2,3,4-tri-O-[(S)-2-methylbutyryl]sucrose and the three regioisomers of 6-O-acetyl-2,3,4-O-[(S)-2-methylbutyryl]-di-O-[(S)-3-methylpentanoyl]sucrose, naturally occurring fatty acid esters of sucrose found in tobacco

796

Synthesis of 6-O-methotrexylhyaluronan as a drug delivery system Original Research Article

797

Synthesis of 6-O-methyl-azithromycin and its ketolide analogue via Beckmann rearrangement of 9(E)-6-O-methyl-erythromycin oxime

798

Synthesis of 6-oxacyclopropa[a]indene derivatives starting from Baylis–Hillman adducts via Pd-mediated C(sp3)–H activation

799

Synthesis of 6-phenyl-2,2′-bipyridine ligands bearing polyaromatic substituents

800

Synthesis of 6-substituted 1-phenylbenzazepines and their dopamine D1 receptor activities Original Research Article

801

Synthesis of 6-substituted 5-cyano-7-hydroxy-2-carboxybenzofurans

802

Synthesis of 6-substituted 7-aryl-5,6-dihydropyrido[2,3-d]pyrimidine(1H,3H)-2,4-diones using the Vilsmeier reaction

803

Synthesis of 6-substituted imidazo[2,1-b]thiazoles via Pd/Cu-mediated Sonogashira coupling in water

804

Synthesis of 6-substituted tetrahydropyridinones and cyclization to indolizidine and quinolizidine structures

805

Synthesis of 6-sulfodisaccharides by beta-N-acetylhexosaminidase-catalyzed transglycosylation

806

Synthesis of 6-thio pseudo glycolipids and their orientation on a gold slide studied by IRRAS

807

Synthesis of 6-vinyl and 5-vinylproline analogues of ascomycin

808

Synthesis of 6Z,8E-heneicosadien-11-one, a sex pheromone of the painted apple moth, Teia anartoides

809

Synthesis of 7- and 10-spermine conjugates of paclitaxel and 10-deacetyl-paclitaxel as potential prodrugs

810

Synthesis of 7-(E)-alkenyl-4-amino-3-quinolinecarbonitriles via Pd-mediated Heck, Stille, and Suzuki reactions

811

Synthesis of 7,8-Benzo-3-hydroxy-9-azabicyclo[3.3.1]non-3-enes by Cyclocondensation of 1,3-Bis-Silyl Enol Ethers with Isoquinolines

812

Synthesis of 7,8-benzo-9-aza-4-oxabicyclo[3.3.1]nonan-3-ones by sequential ‘condensation–iodolactonization’ reactions of 1,1-bis(trimethylsilyloxy)ketene acetals with isoquinolines

813

Synthesis of 7,8-disubstituted benzolactam-V8 and its binding to protein kinase C

814

Synthesis of 7,9-dideoxybaccatin IV analogs from sinenxan A

815

Synthesis of 7′-[123I]iodo-d-luciferin for in vivo studies of firefly luciferase gene expression

816

Synthesis of 7-alkoxy-4-trifluoromethylcoumarins via the von Pechmann reaction catalyzed by molecular iodine

817

Synthesis of 7-amino-3a,4-dihydro-3H-[1]benzopyrano[4,3-c]isoxazole derivatives displaying combined α2-adrenoceptor antagonistic and 5-HT reuptake inhibiting activities Original Research Article

818

Synthesis of 7-aryl-1,8-naphthyridines via addition of aryl boronic acids to 1,8-naphthyridine N-oxides

819

Synthesis of 7-azabicyclo[2.2.1]heptane derivatives via bridgehead radicals

820

Synthesis of 7-azabicyclo[2.2.1]heptane-1,4-dicarboxylic acid, a rigid non-chiral analogue of 2-aminoadipic acid

821

Synthesis of 7-azabicyclo[2.2.1]heptane-1-carboxylate via silver/ThioClickFerrophos-catalyzed asymmetric 1,3-dipolar cycloaddition of dihydropyrrole ester with N-substituted maleimide

822

Synthesis of 7-chloro-2,3-dihydro-2-[1-(pyridinyl)alkyl]-pyridazino[4,5-b]quinoline-1,4,10(5H)-triones as NMDA glycine-site antagonists

823

Synthesis of 7-chloro-4-substituted aminoquinolines and their in vitro ability to produce methemoglobin in canine hemolysate

824

Synthesis of 7-cyano- and 7-acetamido-indoles via cyanocarbonation/hydrogenation of 7-formyl indole

825

Synthesis of 7-cycloalkylimino substituted 3-amino-6-fluoro-2-methyl-3H-quinazolin-4-ones

826

Synthesis of 7-deoxycholic amides or cholanes containing distinctive ion-recognizing groups at C3 and C12 and evaluation for ion-selective ionophores

827

Synthesis of 7-hydroxy-4-methylcoumarin via the Pechmann reaction with Amberlyst ion-exchange resins as catalysts

828

Synthesis of 7-hydroxycoumarins by Pechmann reaction using Nafion resin/silica nanocomposites as catalysts

829

Synthesis of 7-membered cyclic hydroxyguanidines: Novel HIV-1 protease inhibitors

830

Synthesis of 7-methoxybenzolactam-V8 using aminomercuration as a key reaction

831

Synthesis of 7-O-(2-deoxy-2-sulfamido-α-d-glucopyranosyl)-4-methylcoumarin sodium salt: a fluorogenic substrate for sulfamidase

832

Synthesis of 7-O-galloyl-d-sedoheptulose

833

Synthesis of 7-oxa-phomopsolide E and its C-4 epimer

834

Synthesis of 7-oxo-7H-naphtho[1,2,3-de]quinoline derivatives as potential anticancer agents active on multidrug resistant cell lines Original Research Article

835

Synthesis of 7-Substituted Fluoroquinolone Derivatives Contain- ing Triazolidine Dione Moiety and In Vitro Evaluation of Their Cytotoxic Effects

836

Synthesis of 7-thiaarachidonic acid as a mechanistic probe of prostaglandin H synthase-2

837

Synthesis of 7-trifluoromethylpyrazolo[1,5-a]pyridinedicarboxylate

838

Synthesis of 7α- and 7β-spermidinylcholesterol, squalamine analogues

839

Synthesis of 7α-methoxy-2-(1,3-dithiolan-2-ylidene)cephem sulphones. A new series of human leukocyte elastase inhibitors

840

Synthesis of 7α-substituted androstenediones by a 1,4-conjugate addition approach

841

Synthesis of 8-(2′-deoxy-β-d-ribofuranosyl)imidazo[1,2-a]-s-triazin-4-one

842

Synthesis of 8-(S)-methoxy-11-desmethyl laulimalide: a novel laulimalide analogue

843

Synthesis of 8,9-disubstituted fluoranthenes by domino two-fold Heck/electrocyclization/dehydrogenation of 1,2-dibromoacenaphthylene

844

Synthesis of 8-[18F]Fluoroguanine Derivatives: In Vivo Probes for Imaging Gene Expression with Positron Emission Tomography

845

Synthesis of 8-aminoadenosine 5′-(aminoalkyl phosphates), analogues of aminoacyl adenylates Original Research Article

846

Synthesis of 8-aryl substituted benzo[a]phenanthridine derivatives by consecutive three component tandem reaction and 6-endo carbocyclization

847

Synthesis of 8-arylated catechin and epicatechin derivatives via Suzuki cross-coupling

848

Synthesis of 8-arylsulfoxyl/sulfonyl adenines

849

Synthesis of 8-azidooctyl glycoside derivatives of the O-chain repeating unit of Escherichia coli O9a lipopolysaccharide and a methylated analog Original Research Article

850

Synthesis of 8-C-glucosylflavones Original Research Article

851

Synthesis of 8-chloro-benzo[c]quinolizin-3-ones as potent and selective inhibitors of human steroid 5α-reductase 1

852

Synthesis of 8-geranyloxypsoralen analogues and their evaluation as inhibitors of CYP3A4 Original Research Article

853

Synthesis of 8-hydroxyquinoline functionalised DO3A ligand and Eu(III) and Er(III) complexes: Luminescence properties

854

Synthesis of 8-O-alkylshikonin(alkannin)s: new ketal formation, tautomerism, and nucleophilic aromatic substitution

855

Synthesis of 8-oxa analogues of norcocaine endowed with interesting cocaine-like activity

856

Synthesis of 8-R-9c-alkyl-1-aryl-2-benzyl-1-hydroxy-1,2,9b,9c-tetrahydro-5-oxa-2-aza-cyclopenta[2,3]cyclopropa[1,2-a]naphthalene-3,4-diones and reaction thereof with acetic anhydride

857

Synthesis of 8-substituted 5H,9H-6-oxa-7-aza-benzocyclononene-10,11-dione-11-O-methyloximes, a new [1,2]-oxazonine ring system

858

Synthesis of 8-Substituted 7-Azarutaecarpines

859

Synthesis of 8-substituted bicyclo[3.2.1]octane-6-carboxylic acids and anti-convulsant properties of the corresponding amides

860

Synthesis of 8-substituted xanthines via 5,6-diaminouracils: an efficient route to A2A adenosine receptor antagonists

861

Synthesis of 8-thiabicyclo[3.2.1]oct-2-enes and their binding affinity for the dopamine and serotonin transporters

862

Synthesis of 8-vinyladenosine 5′-di- and 5′-triphosphate: evaluation of the diphosphate compound on ribonucleotide reductase

863

Synthesis of 9- and 10-membered macrolactones by selective ozonolysis of 1,4-diazaphenanthrene derivatives

864

Synthesis of 9-(2-β-C-methyl-β-d-ribofuranosyl)-6-substituted purine derivatives as inhibitors of HCV RNA replication

865

Synthesis of 9,9′-biphenanthryl-10,10′-bis(oxazoline)s and their preliminary evaluations in the Friedel–Crafts alkylations of indoles with nitroalkenes

866

Synthesis of 9-[2-O-(2-Methoxyethyl)-β-D-Ribofuranosyl]purines Using 1-Methanesulfonyloxy-2-Methoxyethane

867

Synthesis of 99mTc(CO)3-deoxyuridine derivatives as potential HSV1-tk gene expression imaging agents

868

Synthesis of 99mTc-ciprofloxacin by different methods and its biodistribution

869

Synthesis of 9-alkyl and 9-heteroalkyl substituted 2-amino-6-guanidinopurines and their influence on the NO-production in macrophages Original Research Article

870

Synthesis of 9-alkyl-6-amino[1,2,4]triazolo[3,4-c]-5-azaquinoxalines. Mild and effective SNAr amination of highly electron-poor heterocycles

871

Synthesis of 9-anthrylmethyl-functionalised cyclopentadienyl derivatives of rhodium(I) and iridium(I) and study of their luminescence properties

872

Synthesis of 9-arylamino- and (Z)-9-arylimino-9H-pyrrolo[1,2-a]indoles by reactions of 2-(pyrrol-1-yl)benzaldehydes with aryl amines

873

Synthesis of 9-ethynyl-9-fluorenol and its derivatives for crystallographic and optical properties study

874

Synthesis of 9H-fluoren-9-yl benzodithioates and their application as reversible addition–fragmentation chain transfer agents in living radical polymerization of styrene

875

Synthesis of 9-membered masked enediyne analogues possessing DNA intercalator and sugar moieties

876

Synthesis of 9-oxa-noradamantane derivative, an aesthetically pleasing ‘oxa-basket’

877

Synthesis of 9-oxime-11,12-carbamate ketolides Through a novel N-deamination reaction of 11,12-hydrazonocarbamate ketolide Original Research Article

878

Synthesis of 9-oxiranyl-9H-purine derivatives in β-cyclodextrin cavity

879

Synthesis of 9-substituted tetrahydrodiazepinopurines—asmarine A analogues

880

Synthesis of 9-substituted xanthenes by the condensation of arynes with ortho-hydroxychalcones

881

Synthesis of a (+)-anatoxin-a analogue for monoclonal antibodies production

882

Synthesis of a (B12H11S)2− containing glucuronoside as potential prodrug for BNCT

883

Synthesis of a (piperazin-1-ylmethyl)biaryl library via microwave-mediated Suzuki–Miyaura cross-couplings

884

Synthesis of a (thienylethenyl)benzimidazole platinum acetylide complex

885

Synthesis of a (β-acetamido-α-acetoxyethyl)boronic ester via azido boronic esters

886

Synthesis of a [18F]labeled chelidonine derivative as a possible antitumor agent

887

Synthesis of a [2]benzazepine analogue of clavizepine

888

Synthesis of a [2-Pyridinyl-18F]-labelled fluoro derivative of (−)-Cytisine as a candidate radioligand for brain nicotinic α4β2 receptor imaging with PET Original Research Article

889

Synthesis of a [3.3]biphenylophane, and its photophysical and photochemical properties studied by emission and transient absorption measurements

890

Synthesis of a [6-Pyridinyl-18F]-labelled fluoro derivative of WAY-100635 as a candidate radioligand for brain 5-HT1A receptor imaging with PET Original Research Article

891

Synthesis of a ‘direct-linked’ C-disaccharide from a pyranulose glycoside

892

Synthesis of a ‘twisted’ transition-state analogue of biotin

893

Synthesis of a 1,3,4,5-tetrahydrobenzindole β-ketoester

894

Synthesis of a 1,3,5-benzotriazepine-2,4-dione based library

895

Synthesis of a 1′-α-phenylselenouridine derivative as a synthetic precursor for various 1′-modified nucleosides, via enolization at the 1′-position of 3′,5′-O-TIPDS-2′-ketouridine

896

Synthesis of a 10-membered ring with eleutheside functionality by Nozaki–Hiyama–Kishi coupling

897

Synthesis of a 13C,15N labeled imidazole and characterization of the 2,5-endoperoxide and its decomposition

898

Synthesis of a 14-electron iridium(III) complex with a xanthene-based bis(silyl) chelate ligand (xantsil): A distorted seesaw-shaped four-coordinate geometry and reactions leading to 16-electron complexes

899

Synthesis of a 188Re-HEDP complex using carrier-free 188Re, and a study of its stability

900

Synthesis of a 1α-amino-1-deoxy analogue of forskolin

901

Synthesis of a 1α-C-methyl analogue of 25-hydroxyvitamin D3: interaction with a mutant vitamin D receptor Arg274Leu

902

Synthesis of a 200-member library of squaric acid N-hydroxylamide amides

903

Synthesis of a 2-benzocymantrenylpyridine and further mechanistic insights

904

Synthesis of a 2-indolylphosphonamide derivative with inhibitory activity against yersiniabactin biosynthesis

905

Synthesis of a 3′-naphthamido-LacNAc fluorescein conjugate with high selectivity and affinity for galectin-3 Original Research Article

906

Synthesis of a 3-aminopiperidin-2,5-dione as a conformationally constrained surrogate of the Ala-Gly dipeptide

907

Synthesis of a 3-deoxy-l-iduronic acid containing heparin pentasaccharide to probe the conformation of the antithrombin III binding sequence Original Research Article

908

Synthesis of a 4′,4′-spirothietane-2′, N3-cycloadenosine as a highly constrained analogue of 5′-deoxy-5′-methylthioadenosine (MTA)

909

Synthesis of a 5-alkoxypyrido[3,4-d]pyrimidin-4(3H)-one derivative via directed ortho-metallation of a pyridine analogue

910

Synthesis of a 5-alkoxypyrido[4,3-d]pyrimidin-4(3H)-one derivative via a regioselective Meisenheimer N-oxide rearrangement

911

Synthesis of a 6V-sulfated mannopentasaccharide analogue related to PI-88 Original Research Article

912

Synthesis of a Ag–AgBiTe hybrid nano-segmented structure by a galvanic displacement reaction

913

Synthesis of a benzothiadiazole/thiophene-based oligomer for bulk heterojunction photovoltaic cells

914

Synthesis of a benzotriazole azo dye phosphoramidite for labelling of oligonucleotides

915

Synthesis of a benzotriazole phosphoramidite for attachment of oligonucleotides to metal surfaces

916

Synthesis of a benzyl-protected analog of arenarioside, a trisaccharide phenylpropanoid glycoside Original Research Article

917

Synthesis of a BF2 complex of indol-2-yl-isoindol-1-ylidene-amine: a fully conjugated azadipyrromethene

918

Synthesis of a bicontinuous electrically conductive nanocomposite via in-situ formation of RuO2 nanoparticles

919

Synthesis of a bicyclic analog of l-iduronic acid adopting the biologically relevant 2S0 conformation Original Research Article

920

Synthesis of a bicyclic double-headed nucleoside

921

Synthesis of a bicyclo[5.3.1]undecene by a facile domino enyne cross-metathesis/IMDA

922

Synthesis of a bifunctional hapten designed to mimic both transition state and to induce “bait and switch” catalysis

923

Synthesis of a binuclear copper(II) compound and its use as a copper source for preparation of an environmental catalyst

924

Synthesis of a bio-based polyamidoamine-epichlorohydrin resin and its application for soy-based adhesives

925

Synthesis of a Biochemically Important Aldehyde, 3,4-Dihydroxyphenylacetaldehyde

926

Synthesis of a Biochemically Important Aldehyde, 3,4-Dihydroxyphenylglycolaldehyde

927

Synthesis of a biocompatible gelatin functionalized graphene nanosheets and its application for drug delivery

928

Synthesis of a biocompatible polymer using siloxane-based surfactants in supercritical carbon dioxide

929

Synthesis of a biologically active isomer of kotalanol, a naturally occurring glucosidase inhibitor Original Research Article

930

Synthesis of a bioprobe for elucidation of target molecule of spongean anti-malarial peroxides

931

Synthesis of a biotinated amphiphile

932

Synthesis of a biotin-conjugate of phosmidosine O-ethyl ester as a G1 arrest antitumor drug Original Research Article

933

Synthesis of a biotin-tagged photoaffinity probe of 2-azetidinone cholesterol absorption inhibitors Original Research Article

934

Synthesis of a biotinylated camptothecin derivative and determination of the binding sequence by T7 phage display technology

935

Synthesis of a biphenyl library for studies of hydrogen bonding in the solid state

936

Synthesis of a biphenyl-based axially chiral amino acid as a highly efficient catalyst for the direct asymmetric aldol reaction

937

Synthesis of a biphenyl-based cyclophane via benzidine rearrangement of a constrained m-nitrophenol derivative

938

Synthesis of a bipyridine-derived achiral thiourea trifluoromethanesulfonic acid salt and its application as an additive in organocatalytic asymmetric reactions

939

Synthesis of a bis(diketiminate)bromosamarium(III) complex and its activity in the polymerization of methyl methacrylate Original Research Article

940

Synthesis of a bis-(N-sec-butyl-dithiocarbamato)-nitrido-99mTc complex: a potential new radiopharmaceutical for brain perfusion studies

941

Synthesis of a bis(phenoxyketimine) palladium(II) complex and its activity in the Suzuki–Miyaura reaction

942

Synthesis of a bis-azido analogue of acromelic acid for radioisotope-free photoaffinity labeling and biochemical studies

943

Synthesis of a bi-structured hybrid in a CaO–SiO2-PTMO system and in vitro evaluation on its potential of bone-bonding property

944

Synthesis of a bis-vinylogous chlorin possessing a fused naphthalene ring

945

Synthesis of a boron analogue of glucose-conjugated nucleoside diphosphate: nucleoside α-P-boranodiphosphoglucose

946

Synthesis of a boron analogue of glucose-conjugated nucleoside diphosphate: nucleoside α-P-boranodiphosphoglucose

947

Synthesis of a boron analogue of glucose-conjugated nucleoside diphosphate: nucleoside α-P-boranodiphosphoglucose

948

Synthesis of a boronated amino acid as a potential neutron therapy agent: 1-amino-3-[(dihydroxyboryl)ethyl]cyclobutanecarboxylic acid

949

Synthesis of a boron-containing conducting polymer from the anodic oxidation of Tris(pyrrolyl)borane

950

Synthesis of a branched chain aza-C-disaccharide via the cycloaddition of a chiral nitrone to an alkene, both sugar derivatives

951

Synthesis of a bromotyrosine-derived natural product inhibitor of mycothiol-S-conjugate amidase

952

Synthesis of a building block for phosphonate analogues of moenomycin A12 from d-tartaric acid

953

Synthesis of a building block for phosphonate analogues of moenomycin A12 from d-tartaric acid

954

Synthesis of a C(4)–C(9) eleutheside template from d-glucal

955

Synthesis of a C1 symmetric BINOL–terpyridine ligand and highly enantioselective methyl propiolate addition to aromatic aldehydes

956

Synthesis of a C1–C9 fragment of rhizoxin

957

Synthesis of a C1-symmetric Box macrocycle and studies towards active-template synthesis of mechanically planar chiral rotaxanes

958

Synthesis of a C3-symmetric (1→6)-N-acetyl-β-d-glucosamine octadecasaccharide using click chemistry Original Research Article

959

Synthesis of a C3-symmetric ferrocenylphosphine and its application to the Suzuki reaction of aryl chlorides

960

Synthesis of a C3-symmetric macrocycle with alternating sugar amino acid and tyrosine residues

961

Synthesis of a C8 oxygenated pyranonaphthoquinone: a useful precursor to dimeric pyranonaphthoquinones

962

Synthesis of a caged glutamate for efficient one- and two-photon photorelease on living cells

963

Synthesis of a cam system for the measurement and follow rest of multi-step shaft necks at machining

964

Synthesis of a carbamide-based dithiocarbamate chelator for the removal of heavy metal ions from aqueous solutions

965

Synthesis of a carbon monolith with trimodal pores

966

Synthesis of a carbon nanofiber/carbon foam composite from coal liquefaction residue for the separation of oil and water Original Research Article

967

Synthesis of a carbon nanotube monolith with controlled macroscopic shape

968

Synthesis of a carbon replica of zeolite Y with large crystallite size

969

Synthesis of a carbon-14 analogue of 8-chloro-11-(4-methyl-1-piperazinyl)-11-[14C]-dibenz[b,f][1,4]oxazepine

970

Synthesis of a carbon-14 analogue of N-(aryl-methyl)-3-phenyl-acryl amidine-[carboxy-14C] and its derivatives as NR2B-selective NMDA receptor antagonist

971

Synthesis of a carbon-coated NiO/MgO core/shell nanocomposite as a Pd electro-catalyst support for ethanol oxidation

972

Synthesis of a carboxyl linker containing Pk trisaccharide Original Research Article

973

Synthesis of a carotenobenzoporphyrin from a meso-diphenylporphyrin

974

Synthesis of a caryophyllene isoprenologue, a potential diterpene natural product

975

Synthesis of a cationic pyridoxamine conjugation reagent and application to the mechanistic analysis of an artificial transaminase

976

Synthesis of a cell-permeable analogue of a glycosylphosphatidylinositol (GPI) intermediate that is toxic to the living bloodstream form of Trypanosoma brucei

977

Synthesis of a Ceramide Sphingolipid as a Potential Sex Pheromone of the Hair Crab Erimacrus isenbeckii Using Butane-2,3-diacetal Desymmetrised Glycolic Acid Building Blocks

978

Synthesis of a C-galactopyranosyl-linked N-substituted 1,2-ethylenediamine

979

Synthesis of a C-glucosylated cyclopropylamide and evaluation as a glycogen phosphorylase inhibitor

980

Synthesis of a C-glycosylpyranonaphthoquinone related to medermycin

981

Synthesis of a chemiluminescent probe useful for the purification of steroid 5α-reductase

982

Synthesis of a chiral alcohol using a rationally designed Saccharomyces cerevisiae reductase and a NADH cofactor regeneration system

983

Synthesis of a chiral micelle-like dendrimer with phenylene dendrons and a 1,1′-binaphthyl core

984

Synthesis of a chiral steroid ring D precursor starting from carvone

985

Synthesis of a chitin-based biocomposite for water treatment: Optimization for fluoride removal

986

Synthesis of a chitosan derivative soluble at neutral pH and gellable by freeze–thawing, and its application in wound care

987

Synthesis of a chitosan tetramer derivative, β-d-GlcNAc-(1→4)-β-d-GlcNAc-(1→4)-β-d-GlcNAc-(1→4)-d-GlcN through a partial N-acetylation reaction by chitin deacetylase

988

Synthesis of a chitosan-based chelating resin and its application to the selective concentration and ultratrace determination of silver in environmental water samples Original Research Article

989

Synthesis of a chitosan-linked calix[4]arene chelating polymer and its sorption ability toward heavy metals and dichromate anions

990

Synthesis of a chlorogenin glycoside library using an orthogonal protecting group strategy Original Research Article

991

Synthesis of a chlorothalonil peptide conjugate mimicking protein-bound pesticide residues

992

Synthesis of a cholestane glycoside OSW-1 with potent cytostatic activity Original Research Article

993

Synthesis of a cholesterol-appended Tb–DTPA complex by combined removal of tert-Butyl protecting groups and complexation of terbium(III)

994

Synthesis of a class of new phosphine-oxazoline ligands and their applications in palladium-catalyzed asymmetric addition of arylboronic acids to isatins Original Research Article

995

Synthesis of a C-linked hyaluronic acid disaccharide mimetic Original Research Article

996

Synthesis of a clinoptilolite–Fe system with high Cu sorption capacity Original Research Article

997

Synthesis of a COMC–estradiol conjugate for targeted, tissue-selective cancer chemotherapy

998

Synthesis of a common key intermediate for (−)-tetrodotoxin and its analogs

999

Synthesis of a common trisaccharide fragment of glycoforms of the outer core region of the Pseudomonas aeruginosa lipopolysaccharide

1000

Synthesis of a complementary dimer from mono(imidazolyl)-substituted cobalt(II) porphyrin as a new artificial T-form hemoglobin

بازگشت