<< مقالات لاتين >>
<< بر اساس عنوان >>
1
Synthesis of 2,3-unsaturated glycosides via metal-free Ferrier reaction
2
Synthesis of 2,4- and 2,4,5-substituted oxazoles via a silver triflate mediated cyclization
3
Synthesis of 2,4-, 3,4- and 2,3,4-substituted pyrrolidines by cyclization of neutral C-centered α-aminoalkyl radicals
4
Synthesis of 2,4,5-Tri substituted Imidazoles Using Nano-[Zn-2BSMP]Cl2 as a Schiff Base Complex and Catalyst
5
Synthesis of 2,4,5-triaminocyclohexanecarboxylic acid as a novel 2-deoxystreptamine mimic
6
Synthesis of 2,4,5-triaryl-1H-imidazoles using a potent, green and reusable nano catalyst (FHS/SiO2)
7
Synthesis of 2,4,6-tris(trifluoromethyl)phenyl complexes of gold and thallium
8
Synthesis of 2,4,6-trisubstituted pyrimidines as antimalarial agents Original Research Article
9
Synthesis of 2,4,6-trisubstituted tetrahydropyrans via 6-exo selenoetherification of unsaturated alcohols
10
Synthesis of 2,4-diacetylthiazole and 2,5-diacetylthiazole
11
Synthesis of 2,4-dihydroxyquinazolines using carbon dioxide in the presence of DBU under mild conditions
12
Synthesis of 2,4-dimethyl-6-oxo-2,4-heptadienoic acid derivatives from 2,4,6-trimethylpyrylium salts
13
Synthesis of 2,4-dinitrophenylhydrazine loaded sodium dodecyl sulfate-coated magnetite nanoparticles for adsorption of Hg(II) ions from an aqueous solution
14
Synthesis of 2,4-disubstituted 3-chlorofurans and the effect of the chlorine substituent in furan Diels–Alder reactions
15
Synthesis of 2,5-anhydro-(β-d-glucopyranosyluronate)- and (α-l-idopyranosyluronate)-d-mannitol hexa-O-sulfonate hepta sodium salt
16
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
17
Synthesis of 2,5-di(2-thienyl)-1H-pyrrole N-linked with conjugated bridges
18
Synthesis of 2,5-diaryloxazoles through van Leusen reaction and copper-mediated direct arylation
19
Synthesis of 2,5-Dideoxy-5-Substituted Pyrimidine Nucleosides via Intramolecular Glycosylation
20
Synthesis of 2,5-diethynyl substituted oxepins from trans-1,4-diethynylcyclohexa-2,5-diene-1,4-diols
21
Synthesis of 2,5-difunctionalised-3,3-dimethylpiperidines via ω-halogenated imines
22
Synthesis of 2,5-dihalothiazole-4-carboxylates
23
Synthesis of 2,5-dihydrobenzo[b]oxepines and 5,6-dihydro-2H-benzo[b]oxocines based on a ‘[3+3] cyclization-olefin-metathesis’ strategy
24
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)
25
Synthesis of 2,5-disubstituted-3-cyanoindoles
26
Synthesis of 2,5-thiazole butanoic acids as potent and selective αvβ3 integrin receptor antagonists with improved oral pharmacokinetic properties
27
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
28
Synthesis of 2,6-bis(4R-trialkylsiloxymethyloxazolinyl)pyridines and their use in catalytic asymmetric 1,3-dipolar cycloaddition reactions of nitrones and activated alkenes
29
Synthesis of 2,6-cis-disubstituted 4-methylenetetrahydropyrans by oxy-Michael addition
30
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
31
Synthesis of 2,6-diaryl-1,2-dihydropyridines through a 6π-electrocyclization of N-sulfonylazatrienes
32
Synthesis of 2,6-diaryl-3-(trifluoromethyl)pyridines by regioselective Suzuki–Miyaura reactions of 2,6-dichloro-3-(trifluoromethyl)pyridine
33
Synthesis of 2,6-diaryl-4,4-diphenyldithienosiloles and their luminescent properties
34
Synthesis of 2,6-dichlorobenzonitrile from 2,6-dichlorotoluene by gas phase ammoxidation over VPO catalysts
35
Synthesis of 2,6-dimethyl-9-aryl-9-phosphabicyclo[3.3.1]nonanes: their application to asymmetric synthesis of chiral tetrahydroquinolines and relatives
36
Synthesis of 2,6-dimethylnaphthalene by methylation of methylnaphthalene on various medium and large-pore zeolite catalysts Original Research Article
37
Synthesis of 2,6-dioxabicyclo[3.3.0]octenes by tandem ring-rearrangement/cross metathesis
38
Synthesis of 2,6-dioxatricyclo[3.3.1.03,7]nonanes by intramolecular haloetherification and/or transannular hydroxycyclization of alkenes in [4+3]-cycloadducts
39
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
40
Synthesis of 2,6-disubstituted dihydropyrans via an efficient BiBr3-initiated three component, one-pot cascade
41
Synthesis of 2,6-disubstituted morpholines through regioselective oxiranes ring opening by tosylamide under PTC conditions
42
Synthesis of 2,6-disubstituted piperidine alkaloids from ladybird beetles Calvia 10-guttata and Calvia 14-guttata
43
Synthesis of 2,6-disubstituted pyrido[2,3-b][1,4]oxazines
44
Synthesis of 2,6-disubstituted-7,8-dihydro-6H-pyrano[2,3-6]pyrazines
45
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
46
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
47
Synthesis of 2-[(Z)-1-hydropolyfluoro-1-alkenyl]-4H-3,1-benzoxazin-4-ones
48
Synthesis of 2-[18F]fluoro-image-tyrosine via regiospecific fluoro-de-stannylation
49
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
50
Synthesis of 2-[3,5-substituted pyrazol-1-yl]-4,6-trisubstituted triazine derivatives as antimalarial agents
51
Synthesis of 2-[4-(substituted benzylidene)-5-Oxo- 4,5-dihydro-oxazol-2-ylmethyl]-isoindole-1,3-dione Derivatives as Novel Potential Antimicrobial Agents
52
Synthesis of 2-[5-amino-2,3-dihydro-4H-imidazol-4-ylidene]malononitriles
53
Synthesis of 2-[6-(2,4-Dinitrophenoxy)hexyl]oxiranecarboxylic acid: A selective carnitine palmitoyltransferase-1 inhibitor Original Research Article
54
Synthesis of 2’-(5-Chloro-2-Hydroxybenzylidene) Benzenesulfanohydrazide Schiff Base and its Anti-Ulcer Activity in Ethanol-Induced Gastric Mucosal Lesions in Rats
55
Synthesis of 2′,3′-dideoxy-2′-monofluoromethyl azanucleosides Original Research Article
56
Synthesis of 2′,3′-dideoxy-3′,4′-dihydroxymethyl substituted pyrimidine nucleoside analogues
57
Synthesis of 2′,3′-dideoxy-3′-C-(hydroxymethyl)-4′-thiopentofuranosyl nucleosides as potential antiviral agent
58
Synthesis of 2′,3′-dideoxy-3′-fluoro-l-ribonucleosides as potential antiviral agents from d-sorbitol Original Research Article
59
Synthesis of 2′,3′-dideoxy-6′,6′-difluoro-3′-azanucleosides
60
Synthesis of 2′,3′-dideoxy-6′-fluorocarbocyclic nucleosides via Reformatskii–Claisen rearrangement
61
Synthesis of 2′,3′-dideoxynucleosides via C–S bond cleavage: N-glycosylation of 2,3-dideoxy-1-[(2-pyridylmethyl)thio]glycoside
62
Synthesis of 2′,3′-dihydrosolanesyl analogues of β-d-arabinofuranosyl-1-monophosphoryldecaprenol with promising antimycobacterial activity
63
Synthesis of 2′,5′-oligoadenylate analogs containing an adenine acyclonucleoside and their ability to activate human RNase L
64
Synthesis of 2′-aminoalkyl-1-benzylisoquinoline derivatives and medium sized ring analogues with mu opiod receptor binding activities
65
Synthesis of 2′-C-methyl-branched isonucleosides
66
Synthesis of 2′-C-α-difluoromethylarauridine and its 3′-O-phosphoramidite incorporation into a hammerhead ribozyme
67
Synthesis of 2′-dealkylmumbaistatin
68
Synthesis of 2′-deoxy-2′-fluororibo- and 2′-deoxy-2′,2′-difluororibonucleosides derived from 6-(het)aryl-7-deazapurines
69
Synthesis of 2′-deoxyibosylnucleosides using new 2′-deoxyribosyltransferase microorganism producers
70
Synthesis of 2′-deoxyuridine 5′-(α,β-imido)triphosphate: a substrate analogue and potent inhibitor of dUTPase Original Research Article
71
Synthesis of 2′-hydrazine oligonucleotides and their efficient conjugation with aldehydes and 1,3-diketones
72
Synthesis of 2′-O,3′-O bicyclic adenosine analogues using ring closing metathesis
73
Synthesis of 2′-O-[2-[(N,N-dialkylamino)oxy]ethyl]-modified oligonucleotides: hybridization affinity, resistance to nuclease, and protein binding characteristics
74
Synthesis of 2′-O-modified adenosine building blocks and application for RNA interference Original Research Article
75
Synthesis of 2′-O-α-d-ribofuranosyladenosine, monomeric unit of poly(ADP–ribose)
76
Synthesis of 2′-paclitaxel methyl 2-glucopyranosyl succinate for specific targeted delivery to cancer cells
77
Synthesis of 2′-β-C-methyl toyocamycin and sangivamycin analogues as potential HCV inhibitors
78
Synthesis of 2′-β-C-methyl-neplanocin derivatives as anti-HCV agents
79
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
80
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
81
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
82
Synthesis of 21,31-O-(propane-1,2-diyl)- and 21,31-O-(3-hydroxypropane-1,2-diyl)-cyclomaltoheptaose
83
Synthesis of 21-nor-22-oxa-1α,25-dihydroxyvitamin D3 derivatives in quest of a drug with low calcemic activity
84
Synthesis of 21-oxoporphyrin building blocks and energy donor appended systems
85
Synthesis of 21-thia and 21-oxaporphyrin building blocks and boron–dipyrrin appended systems
86
Synthesis of 22-oxaspiro[4.5]decane CD-ring modified analogs of 1α,25-dihydroxyvitamin D3
87
Synthesis of 25-aminosterols, new antifungal agents
88
Synthesis of 26,27-bisnorcastasterone analogs and analysis of conformation–activity relationship for brassinolide-like activity Original Research Article
89
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
90
Synthesis of 28-19F-amphotericin B methyl ester
91
Synthesis of 2-acetamido-1,2-dideoxy-d-galacto-nojirimycin [DGJNAc] from d-glucuronolactone: the first sub-micromolar inhibitor of α-N-acetylgalactosaminidases
92
Synthesis of 2-acetamido-2-deoxy-5-thio-β-d-altropyranose
93
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)
94
Synthesis of 2-acetamido-3-O-acetyl-2-deoxy-d-mannose phosphoramidites
95
Synthesis of 2-acetoxy[5]helicene by sequential double aromatic oxy-Cope rearrangement
96
Synthesis of 2-acylamino-2-deoxy-d-glucofuranoses and their transformation into hex-2-enofuranoses
97
Synthesis of 2-acylindole-3-acetic acids: a novel base-mediated indole synthesis
98
Synthesis of 2-alkoxy-8-hydroxyadenylpeptides: Towards synthetic epitope-based vaccines
99
Synthesis of 2-alkoxymethyl-3-trifluoromethyl-1,4-naphthoquinones
100
Synthesis of 2-alkyl (and aryl)-1-aryl-2-propen-1-ones via m-CPBA mediated oxidation of γ-(benzotriazol-1-yl)allylic selenides
101
Synthesis of 2-alkyl-2-arylcyanoacetates via CuI/sodium picolinate-catalyzed direct arylation of α-substituted cyanoacetates
102
Synthesis of 2-alkyl-3-aryl-substituted quinuclidines as novel dopamine transporter inhibitors
103
Synthesis of 2-alkylidene-cycloalkane-1,3-diols via enantioselective intramolecular carbolithiation
104
Synthesis of 2-alkylidenetetrahydrofurans by Ru-catalyzed regio- and stereoselective codimerization of dihydrofurans with ,(alpha),(beta)-unsaturated esters
105
Synthesis of 2-alkynylquinolines from 2-chloro and 2,4-dichloroquinoline via Pd/C-catalyzed coupling reaction in water
106
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
107
Synthesis of 2-amido-3-hydroxypyridin-4(1H)-ones: novel iron chelators with enhanced pFe3+ values Original Research Article
108
Synthesis of 2-amino-1,3,4-oxadiazoles from isoselenocyanates via cyclodeselenization
109
Synthesis of 2-amino-1,3-dienes by chromium-catalyzed addition of silylated propargyl bromides to imines
110
Synthesis of 2-amino-1,3-diols incorporating the cyclobutane ring
111
Synthesis of 2-amino-2,4-anhydro-3-O-(2-tetrahydropyranyl)-psicofuranose: a versatile intermediate for S-type locked nucleosides
112
Synthesis of 2-Amino-3,5-dicarbonitrile-6-thiopyridines Using Silica-bonded N-Propyldiethylenetriamine as a Heterogeneous Solid Base Catalyst
113
Synthesis of 2-amino-3-cyano-4H-chromen-4-ylphosphonates and 2-amino-4H-chromenes catalyzed by tetramethylguanidine
114
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
115
Synthesis of 2-amino-4-(4-methoxyphenyl)-1,3-thiazole coatedmagnetic nanoparticles: A potential antibacterial compound
116
Synthesis of 2-amino-4-(7-azaindol-3-yl)pyrimidines as cyclin dependent kinase 1 (CDK1) inhibitors
117
Synthesis of 2-amino-4,6-diarylnicotininitriles using 3-propyldiethylenetriamine-silica as a recyclable solid base catalyst
118
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
119
Synthesis of 2-Amino-4H-chromene Derivatives under Solvent-Free Condition Using MOF-5
120
Synthesis of 2-amino-4H-pyran derivatives in aqueous media with nano-SnO2 as recyclable catalyst
121
Synthesis of 2Amino4hydroxy1HPyrrole3Carbonitrile from Glycine Under Microwave Irradiation
122
Synthesis of 2-amino-5-alkylidenethiazol-4-ones from ketones, rhodanine, and amines with the aid of re-usable heterogeneous silica-pyridine based catalyst
123
Synthesis of 2-amino-5-chloro-3-(trifluoromethyl)benzenethiol and conversion into 4H-1,4-benzothiazines and their sulfones
124
Synthesis of 2-amino-5-substituted-1,3,4-oxadiazoles using 1,3-dibromo-5,5-dimethylhydantoin as oxidant
125
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
126
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
127
Synthesis of 2-amino-8-chloro-4-phenyl-5,11-dihydro-6H-pyrido[2,3-a]carbazole-3-carbonitrile: Structural and biological evaluation
128
Synthesis of 2-aminoazulene derivatives. Nucleophilic and palladium-catalyzed amination of 2-substituted azulene
129
Synthesis of 2-aminobenzoxazoles via copper-catalyzed electrophilic amination of benzoxazoles with O-benzoyl hydroxylamines
130
Synthesis of 2-aminocyclopropyl pyrrolidines from glycoaminonitriles
131
Synthesis of 2-aminoethyl-5-carbethoxythiazoles utilizing a Michael-like addition strategy
132
Synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolin-1-ols and their conversion to 7-aryl-9H-6-oxa-5,8-diaza-benzocycloheptenes
133
Synthesis of 2-aryl-1h-benzimidazole derivatives using nano montmorillonite clay as an efficient catalyst
134
Synthesis of 2-aryl1-H-benzo[d]imidazole derivatives using nano montmorillonite clay as an efficient catalyst
135
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
136
Synthesis of 2-aryl-2H-indazoles by base catalysed reaction of 2-nitrobenzyl triphenylphosphonium bromide and aryl isocyanates
137
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
138
Synthesis of 2-aryl-3-hydroxymethyl-5,5-difluoropiperidines
139
Synthesis of 2-aryl-4-chloropyrroles via ring expansion of 2-aryl-1-chlorocyclopropanecarbaldehydes
140
Synthesis of 2-aryl-4H-pyrano[2,3-b]pyridin-4-ones by a one-pot deprotection–cyclization reaction
141
Synthesis of 2-aryl-6-methyl-5-nitroquinoline derivatives as potential prodrug systems for reductive activation
142
Synthesis of 2-arylacrylic esters from aryl methyl ketones via Wittig reaction/singlet oxygen ene reaction
143
Synthesis of 2-arylbenzimidazoles via microwave Suzuki–Miyaura reaction of unprotected 2-chlorobenzimidazoles
144
Synthesis of 2-arylbenzoxazoles via DDQ promoted oxidative cyclization of phenolic Schiff bases—a solution-phase strategy for library synthesis
145
Synthesis of 2-aryl-imidazo[4,5-d][1,2,3]triazoles from a 4-nitro-imidazol-5-yl phosphoramidate and aryl isocyanates
146
Synthesis of 2-arylpropionic acids by electrocarboxylation of benzylchlorides catalysed by PdCl2(PPh3)2
147
Synthesis of 2-azaspiro[4.4]nonan-1-ones via phosphine-catalysed [3+2]-cycloadditions
148
Synthesis of 2-azidoethyl α-d-mannopyranoside orthogonally protected and selective deprotections
149
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
150
Synthesis of 2-benzyl-2H-pyrazole-3,4-diamine dihydrochloride
151
Synthesis of 2-benzylimidazo[2,1-b][1,3]benzothiazoles through palladium-catalyzed heteroannulation of acetylenic compounds
152
Synthesis of 2-boryl-1,3-butadienes from tributylphosphine stabilized zirconacyclopropenes and alkynes
153
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
154
Synthesis of 2-bromo-1H-indenes via copper-catalyzed intramolecular cross-coupling of gem-dibromoolefins
155
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
156
Synthesis of 2-chloro-1,1-difluoroallyl mesylates through novel rearrangement and CC bond formation by their Pd-catalyzed reaction with diethylzinc
157
Synthesis of 2-chloro-4-nitrophenyl α-l-fucopyranoside: a substrate for α-l-fucosidase (AFU)
158
Synthesis of 2-chloro-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one
159
Synthesis of 2-C-hydroxymethylribofuranosylpurines as potent anti-hepatitis C virus (HCV) agents
160
Synthesis of 2-C-methylerythritols and 2-C-methylthreitols via enantiodivergent Sharpless dihydroxylation of trisubstituted olefins
161
Synthesis of 2-C-trifluoromethyl substituted d-ribose
162
Synthesis of 2-cyano-1,4-cycloheptadiene derivatives via divinylcyclopropane rearrangement and alkylation of novel cycloheptadienyl anion species
163
Synthesis of 2D metal–organic coordination polymers with large internal cavities and their magnetic properties
164
Synthesis of 2D polymeric dicyanamide bridged hexa-coordinated Cu(II) complex: Structural characterization, spectral studies and TDDFT calculation
165
Synthesis of 2-Dehydro-3-epi-20-hydroxyecdysone
166
Synthesis of 2-deoxy cyclic and linear oligosaccharides by oligomerization of monomers Original Research Article
167
Synthesis of 2-deoxy-2-(4-nitroimidazol-1-yl)-d-alditols
168
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
169
Synthesis of 2-Deoxy-2-C-Alkylglucosides of myo-Inositol as possible inhibitors of a N-Deacetylase enzyme in the biosynthesis of mycothiol
170
Synthesis of 2-deoxy-2-fluoro analogs of polyprenyl β-d-arabinofuranosyl phosphates
171
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
172
Synthesis of 2-deoxy-2-fluoro-glucotropaeolin, a thioglucosidase inhibitor
173
Synthesis of 2-deoxy-2-fluoro-phosphatidylinositol-4,5-bisphosphate and analogues: Probes and modulators of the mammalian PI-PLCS
174
Synthesis of 2-deoxy-d-arabino/lyxo-hexopyranosyl disaccharides Original Research Article
175
Synthesis of 2-deoxy-hexopyranosyl derivatives of uridine as donor substrate analogues for glycosyltransferases
176
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)
177
Synthesis of 2-Diphenylphosphinoyl-2 -Halo Biphenyls Via Suzuki-Miyaura Coupling as Possible Route to Non-Symmetric Biphenyl Phosphines
178
Synthesis of 2-diphenylphosphinoyl-3,5-(diaryl)-3,4-dihydro-2H-thiopyrans by the reaction of a bis[(diphenylphosphinoyl)methyl]sulfide with chalcones
179
Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride
180
Synthesis of 2E,4E,6E,11Z-octadecatetraenoic acid of the Rhizobium leguminosarum biovar viciae Nod factor
181
Synthesis of 2-ethyl-2-hexenal oxime and its flotation performance for copper ore
182
Synthesis of 2-ferrocenylquinoline derivatives and evaluation of their antimalarial activity
183
Synthesis of 2-fluoro and 4-fluoro galactopyranosyl phosphonate analogues of UDP-Gal Original Research Article
184
Synthesis of 2-fluoronoraristeromycin and its inhibitory activity against Plasmodium falciparum S-Adenosyl- -homocysteine hydrolase
185
Synthesis of 2-fluorotetralones by oxidative radical cyclization of α-fluoroacetophenones and olefins
186
Synthesis of 2H-1,2-oxaphosphorin 2-oxides
187
Synthesis of 2H-1,4-benzothiazin-3(4H)-ones and 2H-1,4-benzoselenazin-3(4H)-ones with the aid of samarium(II) iodide
188
Synthesis of 2H-1,5-benzodioxepin and 2,5-dihydro-1,6-benzodioxocin derivatives via ring-closing metathesis reaction
189
Synthesis of 2-halo-2H-azirines
190
Synthesis of 2H-chromenes and 1,2-dihydroquinolines from aryl aldehydes, amines, and alkenylboron compounds
191
Synthesis of 2H-pyrroles by treatment of pyrrolidines with DDQ
192
Synthesis of 2H-pyrroles via the 1,3-dipolar cycloaddition reaction of nitrile ylides with acrylamides
193
Synthesis of 2-hydroxy acid from 2-amino acid by Clostridium butyricum
194
Synthesis of 2-hydroxy-3-indolinones and 3-hydroxy-2-indolinones by anionic cyclization, in situ oxidation and rearrangement
195
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
196
Synthesis of 2-hydroxy-3-substituted naphthoquinones using the Heck reaction
197
Synthesis of 2-imidazolidinylidene propanedinitrile derivatives as stimulators of gastrointestinal motility—III Original Research Article
198
Synthesis of 2-iminothiazoline derivatives by sequential conjugate addition/annulation/ring-opening reactions
199
Synthesis of 2-iodo- and 2-phenyl-[11C]melatonin: potential PET tracers for melatonin binding sites
200
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
201
Synthesis of 2-iodoynamides and regioselective [2+2] cycloadditions with ketene
202
Synthesis of 2-isoxazoline and α-hydroxy ketomethylene dipeptide isosteres Original Research Article
203
Synthesis of 2-mercapto-3-substituted-5,6-dimethylthieno[2,3-d] pyrimidin-4(3H)-ones as new analgesic, anti-inflammatory agents
204
Synthesis of 2-Mercaptobenzimidazole and Some of its Derivatives
205
Synthesis of 2-mesityl-3-methylpyrrole via the Trofimov reaction for a new BODIPY with hindered internal rotation
206
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
207
Synthesis of 2-methyl- and 2-methylenecyclobutane amino acids
208
Synthesis of 2-methyl-4-methoxydiphenylamine by palladium catalyzed C–N coupling—high synthetic versatility by use of a flexible catalytic system
209
Synthesis of 2-methylidene-1-silacyclohexanes by intramolecular hydrosilylation
210
Synthesis of 2-methylidene-1-silacyclohexanes from 2,6-dibromohex-1-ene and polyhalosilanes
211
Synthesis of 2-modified aristeromycins and their analogs as potent inhibitors against Plasmodium falciparum S-adenosyl-l-homocysteine hydrolase Original Research Article
212
SYNTHESIS OF 2-MONO- AND 2,7-DISUBSTITUTED-1,8-DIHYDROXY9-ANTHRONES, A NOVEL MEMBER OF THE ANTHRONE CLASS OF ANTIPSORIATIC AGENTS
213
Synthesis of 2-monoacylglycerols and structured triacylglycerols rich in polyunsaturated fatty acids by enzyme catalyzed reactions
214
Synthesis of 2-N-alkyl(aryl)amino-7-nitrobenzothiazoles
215
Synthesis of 2-naphthylacrylamides and 2-naphthylacrylates via homogeneous catalytic carbonylation of 1-iodo-1-naphthylethene derivatives
216
Synthesis of 2-NBDLG, a fluorescent derivative of l-glucosamine; the antipode of d-glucose tracer 2-NBDG
217
Synthesis of 2-N-substituted benzothiazoles via domino condensation-hetero cyclization process, mediated by copper oxide nanoparticles under ligand-free conditions
218
Synthesis of 2-O-(2-iodoethyl)-d-glucose, a stable iodinated analogue of 2-deoxy-2-fluoro-d-glucose
219
Synthesis of 2-O-heteroaroyl taxanes: evaluation of microtubule assembly promotion and cytotoxicity
220
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
221
Synthesis of 2-oxazolidinones by salen-Co-complexes catalyzed oxidative carbonylation of β-amino alcohols
222
Synthesis of 2-oxazolidones by sulfur-assisted thiocarboxylation with carbon monoxide and oxidative cyclization with molecular oxygen under mild conditions
223
Synthesis of 2-oxazolines and related N-containing heterocycles using [Et2NSF2]BF4 as a cyclodehydration agent
224
Synthesis of 2-oxazolines mediated by N,N′-diisopropylcarbodiimide
225
Synthesis of 2-oxazolines via boron esters of N-(2-hydroxyethyl) amides
226
Synthesis of 2-pentafluorosulfanylnaphthalene
227
Synthesis of 2-phenylethyl acetate in the presence of Yarrowia lipolytica KKP 379 biomass
228
Synthesis of 2-phenylquinoline-based ambipolar molecules containing multiple 1,3,4-oxadiazole spacer groups
229
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
230
Synthesis of 2-pyranosyl benzothiazoles, benzimidazoles and benzoxazoles via nucleophilic addition reactions of pyranosyl nitrile oxides
231
Synthesis of 2-pyranylidene or (2-furyl)carbene–chromium complexes from conjugated enyne carbonyl compounds with Cr(CO)5(THF)
232
Synthesis of 2-pyridones as tissue factor VIIa inhibitors
233
Synthesis of 2-pyrolyl-2-hydroxy-2-cyanoacetamide through FeCl3–TBHP mediated hydroxylation of captodative stabilized radical intermediate
234
Synthesis of 2-pyrone-4-carboxaldehydes from acetylene dicarboxaldehyde monoacetal
235
Synthesis of 2S-(2-hydroxyethyl)-3R-hydroxy-4S-(thymin-1-yl or adenin-9-yl)-tetrahydrofuran
236
Synthesis of 2-selenoxoperhydro-1,3-selenazin-4-ones via diselenocarbamate intermediates
237
Synthesis of 2-Substitued Benzimidazoles Using P2O5-SiO2
238
Synthesis of 2-Substitued Benzimidazoles Using P2O5-SiO2
239
Synthesis of 2-substituted -tryptophan-containing peptide derivatives with endothelin receptor antagonist activity
240
Synthesis of 2-substituted 1-benzyl-2,3,4,5-tetrahydro-1-benzazepines by palladium catalysis. Observation of a competitive β-hydride elimination pathway
241
Synthesis of 2-substituted 2H-chromenes using potassium vinyltrifluoroborates
242
Synthesis of 2-substituted 3-ethyl-3H-imidazo[4,5-b]pyridines catalyzed by Al3+-exchanged K10 clay as solid acids
243
Synthesis of 2-substituted bamipine derivatives
244
Synthesis of 2-Substituted Benzimidazoles and Bis-benzimidazoles by Microwave in the Presence of Alumina-Methanesulfonic Acid
245
Synthesis of 2-substituted chromenes via ring-closing metathesis and stable 1-benzopyrylium ions
246
Synthesis of 2-substituted endo-hymenialdisine derivatives
247
Synthesis of 2-substituted indoles by palladium-catalyzed heteroannulation with Pd–NaY zeolite catalysts
248
Synthesis of 2-substituted indoles via a palladium-catalyzed domino Heck reaction and dealkylation
249
Synthesis of 2-substituted piperazines via direct α-lithiation
250
Synthesis of 2-substituted pyrrolidines from nitriles
251
Synthesis of 2-substituted quinones, vitamin K3, and vitamin K1 from p-cresol. BF3·OEt2-catalyzed methyl migration of 4-tert-butyldioxycyclohexadienones
252
Synthesis of 2-substituted-7-azaindoles from 2-amino-3-picolin
253
Synthesis of 2-substituted-benzothiazoles by palladium-catalyzed intramolecular cyclization of o-bromophenylthioureas and o-bromophenylthioamides
254
Synthesis of 2-substituted-pyrrolidinethiourea derivatives and their antagonist effect on vanilloid receptor
255
Synthesis of 2-thioxoimidazolines via reaction of 1-unsubstituted 3-aminoquinoline-2,4-diones with isothiocyanates
256
Synthesis of 2-TIPS-oxazol-5-ylboronic acid pinacol ester: efficient route to 5-(het)aryloxazoles via Suzuki cross-coupling reaction
257
Synthesis of 2-trifluoromethoxyethyl trifluoromethoxyacetate and derived 2-trifluoromethoxyacrylates
258
Synthesis of 2-trifluoromethyl-1(substituted aryl)-4(1H)-quinolones using trifluoroacetamidoyl chlorides
259
Synthesis of 2-trifluoromethylthioacrylate and its derivatives via the Knoevenagel condensation
260
Synthesis of 2-ynamides by direct palladium-catalyzed oxidative aminocarbonylation of alk-1-ynes
261
Synthesis of 2α- and 2β-substituted-14-epi-previtamin D3 and their genomic activity
262
Synthesis of 3- and 5-amino-5-(3)-(pyrrol-2-yl)isoxazoles
263
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
264
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
265
Synthesis of 3-(1H-benzimidazol-2-yl)-5-isoquinolin-4-ylpyrazolo[1,2-b]pyridine, a potent cyclin dependent kinase 1 (CDK1) inhibitor
266
Synthesis of 3-(1H-benzo[d]imidazol-1-yl)isoindolin-1-one derivatives promoted by EtOH–AcOH solvent system
267
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
268
Synthesis of 3-(2-nitroalkyl) indoles by reaction of 3-(1-arylsulfonylalkyl) indoles with nitroalkanes
269
Synthesis of 3-(2-pyridyl)-2-substituted-quinazolin-4(3H)-ones as new analgesic and anti-inflammatory agents
270
Synthesis of 3-(3,4-dihydroxyphenyl)-propionic acid derivatives by N-coupling of amines using laccase
271
Synthesis of 3-(4-heteroaryl-phenyl)-8-oxabicyclo[3.2.1]octane-2-carboxylic acid methyl esters
272
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
273
Synthesis of 3-(benzylideneamino)-2-phenyl-5H-imidazo[1,2-b]pyrazole-7-carbonitriles via a four-component condensation reaction
274
Synthesis of 3-(Trifluoromethyl)benzo[c][1,6]naphthyridines from Substituted 4H-Pyran-4-ones via 4-Amino-5-Aryl-2-(trifluoromethyl)pyridines
275
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
276
Synthesis of 3-(Trimethoxysilyl)PropylMethacrylateFunctionalized GrapheneOxideBased Mixed MatrixMembrane andItsApplication for O2/N2Separation
277
Synthesis of 3-(α- and β-d-arabinofuranosyl)-6-chloro-1,2,4-triazolo[4,3-b]pyridazine Original Research Article
278
Synthesis of 3, 4-Dihydropyrimidin-2-(1H)-ones Using a Hydrogel as a Green and Reusable Catalyst
279
Synthesis of 3,20-disubstituted chlorophyll-a derivatives and reactivity of the substituents
280
Synthesis of 3,3,3-trifluoroprop-1-enyl compounds from some enolizable aldehydes
281
Synthesis of 3,3,4,4-tetrafluoro-1,2-bis(imino)cyclobutanes: A cyclic version of fluorinated α-diimines
282
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
283
Synthesis of 3,3′-neotrehalosadiamine and related 1,1′-aminodisaccharides using disarmed, armed, and superarmed building blocks
284
Synthesis of 3,3-bis(difluoramino)octahydro-1,5,7,7-tetranitro-1,5-diazocine (TNFX), a diversified energetic heterocycle
285
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
286
Synthesis of 3,3-disubstituted oxetane building blocks
287
Synthesis of 3,3-disubstituted oxindoles
288
Synthesis of 3,3-disubstituted oxindoles through Pd-catalyzed intramolecular cyanoamidation
289
Synthesis of 3,3-Disubstituted-2,2-bipyridines from 1,10-Phenanthroline-5,6-quinone
290
Synthesis of 3,4,5-trisubstituted indoles via iterative directed lithiation of 1-(triisopropylsilyl)gramines
291
Synthesis of 3,4-diaryl-1-phenyl-4,5-dihydro-1H-pyrazole-5-carbonitriles via 1,3-dipolar cycloaddition reactions
292
Synthesis of 3,4-dihydrobenzo[g]isoquinoline-1(2H)-ones and 3,4-dihydroisoquinoline-1(2H)-ones skeleton via intramolecular electrophilic cyclization
293
Synthesis of 3,4-Dihydropyrano[c]Chromene Derivatives Using Sulfonic Acid Functionalized Silica (SiO2PrSO3H)
294
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
295
Synthesis of 3,4-dihydropyrimidin-2(1H)-ones and 1,4-dihydropyridines using ammonium carbonate in water
296
Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones Catalyzed by Nafion-H Under Ultrasound Irradiation and Solvent-Free Conditions
297
Synthesis of 3,4-dihydropyrimidin-2-ones (DHPMs) using mesoporous aluminosilicate (AlKIT-5) catalyst with cage type pore structure
298
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
299
Synthesis of 3,4-Dihydropyrimidinones using Nano γ-Al2O3/BF3/ Fe3O4 as an Efficient Magnetic Nanocatalyst under Solvent-free Conditions
300
Synthesis of 3,4-dihydropyrrolo[2,1-a]isoquinolines based on [3+2] cycloaddition initiated by Rh2(cap)4-catalyzed oxidation
301
Synthesis of 3,4-dihydroquinazolin-4-one: selenium-catalyzed reductive N-heterocyclization of N-(2-nitrobenzoyl)amides with carbon monoxide
302
Synthesis of 3,4-Dihydroquinoxalin-2-Amine, Diazepine-Tetrazole and Benzodiazepine-2-Carboxamide Derivatives with the Aid of H6P2W18O62/Pyridino-Fe3O4
303
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
304
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
305
Synthesis of 3,4-disubstituted 2(1H)-quinolinones via intramolecular Friedel–Crafts reaction of N-arylamides of Baylis–Hillman adducts
306
Synthesis of 3,4-disubstituted 2,5-dihydrofurans starting from the Baylis–Hillman adducts via consecutive radical cyclization, halolactonization, and decarboxylation strategy
307
Synthesis of 3,4-disubstituted cinnolines by the Pd-catalyzed annulation of 2-iodophenyltriazenes with an internal alkyne
308
Synthesis of 3,4-disubstituted piperidines by ene cyclisation of 4-aza-1,7-dienes
309
Synthesis of 3,4-disubstituted α-methylene-γ-lactones via sonochemical Barbier-type reaction
310
Synthesis of 3,4-fused cycloalkanopyrroles by 1,3-dipolar cycloaddition
311
Synthesis of 3,4-substituted cyclopentenones via an intramolecular Pauson–Khand reaction of NO linked enynes
312
Synthesis of 3,5,6-trisubstituted α-pyrones from Baylis–Hillman adducts
313
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
314
Synthesis of 3,5-Diaryl Azoline and [1,4] Diazepine Derivatives via Microwave Irradiation
315
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
316
Synthesis of 3,5-diazabicyclo [5.1.0] octenes. A new platform to mimic glycosidase transition states
317
Synthesis of 3,5-difunctionalized 1-methyl-1H-pyrazolo[3,4-b]pyridines involving palladium-mediated coupling reactions
318
Synthesis of 3,5-dioxoalkanoates, 3,5-dioxopimelates and 2,4-dioxoadipates by acylation of 1,3-bis-silyl enol ethers
319
Synthesis of 3,5-disubstituted 1,2,4-oxadiazoles and their behavior of liquid crystallines
320
Synthesis of 3,5-disubstituted 1,2,4-oxadiazoles as peptidomimetic building blocks
321
Synthesis of 3,5-disubstituted 1,2,4-oxadiazoles using ionic liquid-phase organic synthesis (IoLiPOS) methodology
322
Synthesis of 3,5-disubstituted-1,2,4-oxadiazoles using tetrabutylammonium fluoride as a mild and efficient catalyst
323
Synthesis of 3,5-lutidine from propionaldehyde over modified ZSM-5 catalysts Original Research Article
324
Synthesis of 3,6-bicyclolides: A novel class of macrolide antibiotics
325
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
326
Synthesis of 3,6-branched arabinogalactan-type tetra- and hexasaccharides for characterization of monoclonal antibodies Original Research Article
327
Synthesis of 3,6-branched oligomannoside fragments of the mannan from Candida albicans cell wall corresponding to the antigenic factor 4 Original Research Article
328
Synthesis of 3,6-diazabicyclo[3.1.1]heptanes as novel ligands for neuronal nicotinic acetylcholine receptors
329
Synthesis of 3,6-diazabicyclo[3.1.1]heptanes as novel ligands for the opioid receptors Original Research Article
330
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
331
Synthesis of 3,6-dioxa-Δ7-4-trifluoromethyl perfluorooctyl trifluoromethyl sulfonimide: bis[(perfluoroalkyl)sulfonyl] superacid monomer and polymer
332
Synthesis of 3,6-epoxy[1,5]dioxocines from 2-hydroxyaromatic benzaldehydes
333
Synthesis of 3,7-dihydroimidazo[1,2a]pyrazine-3-ones and their chemiluminescent properties
334
Synthesis of 3,8,13,18-tetrachloro-2,7,12,17-tetramethoxyporphyrin
335
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
336
Synthesis of 3/8-carbonylated chlorophyll derivatives and regiodependent reductivity of their carbonyl substituents
337
Synthesis of 3-[(N-carboalkoxy)ethylamino]-indazole-dione derivatives and their biological activities on human liver carbonyl reductase Original Research Article
338
Synthesis of 3-[2-(1,3-butadienyl)]-1H-indoles en route to murrapanine analogue
339
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
340
Synthesis of 3′-, 4′- and 6′-deoxy and other analogues of d-glucosaminylphosphatidylinositol
341
Synthesis of 3′,4′-epoxynoraristeromycin analogs for molecular labeling probe of S-adenosyl-l-homocysteine hydrolase Original Research Article
342
Synthesis of 3′-allylindoline spirobenzopyrans derived from 3-allyl-3H-indoles
343
Synthesis of 3′-azido-4′-ethynyl-3′,5′-dideoxy-5′-norarabinouridine: a new anti-HIV nucleoside analogue
344
Synthesis of 3′-C-substituted thymidine derivatives by free-radical techniques: scope and limitations
345
Synthesis of 3′-deoxy-3′-C-methyl nucleoside derivatives Original Research Article
346
Synthesis of 3′-deoxy-3′-C-methyl-β-d-ribonucleoside analogs
347
Synthesis of 3′-O-phosphonomethyl nucleosides with an adenine base moiety
348
Synthesis of 30 wt%BAS/Si3N4 composite by spark plasma sintering
349
Synthesis of 32-nitro-chlorophyll-a derivatives and their electronic absorption/emission data
350
Synthesis of 32-substituted bacteriochlorophyll-d analogs and their self-aggregation in a nonpolar organic solvent
351
Synthesis of 35–40 mers of RNA oligomers from unblocked monomers. A simple approach to the RNA world
352
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
353
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
354
Synthesis of 3-acetamido-1,2,4-tri-O-acetyl-3,5-dideoxy-5-C-[(R)- and (S)-phenylphosphinyl]-α- and -β-d-xylopyranoses
355
Synthesis of 3-acetonyl- and 3-(2-oxoethyl)glutarates
356
Synthesis of 3-acyltetrahydrofurans from formaldehyde acetals of allylic diols
357
Synthesis of 3-alkenyl-2-arylchromones and 2,3-dialkenylchromones via acid-catalysed retro-Michael ring opening of 3-acylchroman-4-ones
358
Synthesis of 3-alkoxycarbonyl-1β-methylcarbapenem using palladium-catalyzed amidation of vinyl halide
359
Synthesis of 3-alkyl naphthalenes as novel estrogen receptor ligands
360
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
361
Synthesis of 3-alkyl-1-isoindolinones by alkylation of a benzotriazolyl substituted N-dimethylamino-phthalimidine
362
Synthesis of 3-alkyl-5-hydroxycyclohex-2-enones via aldolic addition/sulfinate elimination tandem reactions
363
Synthesis of 3-alkylidene-piperidin-4-ones via one-pot cascade transylidation–olefination
364
Synthesis of 3-alkyloxazolidin-2,4-diones using 2-chloroacetamides, carbon dioxide and 1,8-diazabicyclo[5.4.0]undecene (DBU)
365
Synthesis of 3-amido-3-deoxy-β-d-talopyranosides: all-cis-substituted pyranosides as lectin inhibitors
366
SYNTHESIS OF 3-AMINO-1-PHENYL-1H-PYRAZOLE-4, 5-DIONE-4-ARYLHYDRAZONES AS FAST DYES
367
Synthesis of 3-amino-5H-pyrrolo[2,3-e]-1,2,4-triazines by Sonogashira/copper(I)-catalyzed heteroannulation
368
Synthesis of 3-amino-5-methyl-[1,1 -biaryl]-2,4-dicarbonitriles using ZnFe2O4 magnetic nanoparticles
369
Synthesis of 3-aminoaspartic acid derivatives from glycine precursors
370
Synthesis of 3-aminoindole derivatives: combination of Thorpe–Ziegler cyclization and unexpected allylindium-mediated decyanation
371
Synthesis of 3-aminopyrrolidines and piperidines from endocyclic enamine derivatives
372
Synthesis of 3-aminopyrrolidines by cyclization of neutral C-centered α-aminoalkyl radicals
373
Synthesis of 3-aryl substituted benzo[1,2,5]triazepin-4-ones via intramolecular imine formation
374
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
375
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
376
Synthesis of 3-aryl-4-chalcogen-2H-benzopyrans from 3-iodo-4-chalcogen-2H-benzopyrans using a Suzuki cross-coupling
377
Synthesis of 3-aryl-4-methyl-1,2-benzenedisulfonimides, new chiral Brønsted acids. A combined experimental and theoretical study
378
Synthesis of 3-arylcoumarins through N-heterocyclic carbene catalyzed condensation and annulation of 2-chloro-2-arylacetaldehydes with salicylaldehydes
379
Synthesis of 3-arylcoumarins via Suzuki-cross-coupling reactions of 3-chlorocoumarin
380
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
381
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
382
Synthesis of 3-Aryl-Substituted Tetrahydropyran-4-ones and Tetrahydrothiopyran-4-ones
383
Synthesis of 3-azabicyclo[4.1.0]heptane-1-carboxylic acid
384
Synthesis of 3-azido-3-deoxy-β-d-galactopyranosides Original Research Article
385
Synthesis of 3-benzazepines and azepino[4,5-b]heterocyclic ring systems via intramolecular Friedel–Crafts cyclization
386
Synthesis of 3-benzyl-2-substituted quinoxalines as novel monoamine oxidase A inhibitors
387
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
388
Synthesis of 3-buten-1-ol from 1,4-butanediol over indium oxide Original Research Article
389
Synthesis of 3-C-(6-O-acetyl-2,3,4-tri-O-benzyl-α-d-mannopyranosyl)-1-propene: a caveat
390
Synthesis of 3-C-(methyl β-d-xylofuranosid-3-yl)-5-phenyl-1,2,4-oxadiazole
391
Synthesis of 3-chloroanthranilates from α,γ,γ-trichloro-β-iminoesters
392
Synthesis of 3-C-Spiro Ring Nucleoside Analogues, of Possible Biological Activity
393
Synthesis of 3-cyano-2-fluoropyridines
394
Synthesis of 3-cyclohexylpropyl caffeate from 5-caffeoylquinic acid with consecutive enzymatic conversions in ionic liquid
395
Synthesis of 3D hierarchical Ag microspheres assembled with dendritic morphology
396
Synthesis of 3D hierarchical porous carbon as an electrode material for electric double layer capacitors
397
Synthesis of 3D hierarchical porous carbon as electrode material for electric double layer capacitors
398
Synthesis of 3-deaza-3-nitro-2′-deoxyadenosine Original Research Article
399
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
400
Synthesis of 3-deoxy-2-ulosonic acid KDO and 4-epi-KDN, a highly efficient approach of 3-C homologation by propargylation and oxidation
401
Synthesis of 3-deoxy-3,3-difluoro-d-ribohexose from gem-difluorohomoallyl alcohol
402
Synthesis of 3-Deoxyclarithromycin through Biotransformation of Clarithromycin by Aspergillus niger and its Antibacterial Activity
403
Synthesis of 3-derivatized pyrroles precursors polymers for functionalization with biomolecules toward biosensor devices
404
Synthesis of 3-dimensional mesoporous silica using a di-block copolymer template
405
Synthesis of 3-fluoro-2-(diethoxyphosphoryl)imidazo[1,2-a]pyridine
406
Synthesis of 3-fluorobenzoyl chloride functionalized magnetic sorbent for highly efficient enrichment of perfluorinated compounds from river water samples
407
Synthesis of 3-fluoroimidazo[1,2-a]pyrimidines and 5-fluoroimidazo[2,1-b][1,3]thiazoles via heterocyclization of (N-heteroarylimino)trifluoropyruvates
408
Synthesis of 3-functionalized 3-methylazetidines
409
Synthesis of 3-halo-2,5-disubstituted furans via CuX mediated cyclization–halogenation reactions
410
Synthesis of 3-halo-analogues of HHQ, subsequent cross-coupling and first crystal structure of Pseudomonas quinolone signal (PQS)
411
Synthesis of 3-hexuloses from 1,2:5,6-di-O-isopropylidenehexitols
412
Synthesis of 3H-labeled Efomycine M
413
Synthesis of 3H-labeled N-(3-iodoprop-2E-enyl)-2β-carbomethoxy-3β-(4-methylphenyl)nortropane (PE2I) and its interaction with mice striatal membrane fragments
414
Synthesis of 3H-spiro[benzofuran-2,1′-cyclohexane] derivatives from naturally occurring filifolinol and their classical complement pathway inhibitory activity
415
Synthesis of 3-hydroxyindolin-2-one alkaloids, (±)-donaxaridine and (±)-convolutamydines A and E, through enolization–Claisen rearrangement of 2-allyloxyindolin-3-ones
416
Synthesis of 3I-O and 2I-O-monosubstituted derivatives of per-6-azido-β-cyclodextrin—potential molecular scaffolds Original Research Article
417
Synthesis of 3-iodobenzo[b]thiophenes via iodocyclization/etherification reaction sequence
418
Synthesis of 3-iodothiophenes via iodocyclization of (Z)-thiobutenynes
419
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
420
Synthesis of 3-methoxyquinolines via cyclization of 1-isocyano-2-(2-lithio-2-methoxyethenyl)benzenes
421
Synthesis of 3-methoxy-quinoxalin-2-ones from methyl trimethoxyacetate and phenylenediamines
422
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
423
Synthesis of 3-methyl-2-cyclohexenones catalyzed by mercury(II) salts and their microwave assisted BiCl3 catalyzed aldol condensations
424
Synthesis of 3-methyl-4-arylmethylene isoxazole-5(4H)-ones by visible light in aqueous ethanol
425
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
426
Synthesis of 3-methyleneisoindolin-1-ones via palladium-catalyzed C–Cl bond cleavage and cyclocarbonylation of ortho-chloro ketimines
427
Synthesis of 3-Nitro-lH-indole-2-carboxylic Acid Ethyl Ester Derivatives from Baylis-Hillman Adducts
428
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
429
Synthesis of 3-O-acyl/3-benzylidene/3-hydrazone/3-hydrazine/17-carboxyacryloyl ester derivatives of betulinic acid as anti-angiogenic agents
430
Synthesis of 3-O-methylviridicatin analogues with improved anti-TNF-α properties
431
Synthesis of 3-O-sulfoglucuronyl lacto-N-neotetraose 2-aminoethyl glycoside and biotinylated neoglycoconjugates thereof Original Research Article
432
Synthesis of 3-oxagranatane-type alkaloid analogs from carbohydrates
433
Synthesis of 3-Oxa-guaianolides from Santonin
434
Synthesis of 3-oxo oxacycloalkenes by ring closing metathesis
435
Synthesis of 3-oxo-4-benzoyl-1-phenylsuccinimide and its reactions with 1,2- dinucleophiles
436
Synthesis of 3-oxooxa- and 3-oxoazacycloalk-4-enes by ring-closing metathesis. Application to the synthesis of an inhibitor of cathepsin K
437
Synthesis of 3-pentanone from 1-propanol over CeO2–Fe2O3 catalysts Original Research Article
438
Synthesis of 3-Phenyl-2,1-benzisoxazoles via Conversion of Diethyl α-(o-Nitroaryl)benzylphosphonates
439
Synthesis of 3-phenylnaphthalenic derivatives as new selective MT2 melatoninergic ligands Original Research Article
440
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
441
Synthesis of 3-Phenylsulfanyl-1,2-dihydronaphthalenes from Methylenecyclopropanes and Benzenethiol
442
Synthesis of 3-pyrroline via domino Heck–aza-Michael reaction
443
Synthesis of 3-pyrroline-2-ones from amino acids and an aryl amine
444
Synthesis of 3-quinolinecarboxylic acid esters from the Baylis–Hillman adducts of 2-halobenzaldehyde N-tosylimines
445
Synthesis of 3-S-alkyl-3-thio-d-glucose derivatives as new non-ionic surfactants and calcium antagonists
446
Synthesis of 3-silyl-2(5H)-furanone by rhodium-catalyzed cyclocarbonylation
447
Synthesis of 3-spiropyrrolidine-3-spirooxindoles from Baylis–Hillman adducts of chromone with azomethine ylides via [3+2] cycloaddition reaction
448
Synthesis of 3-substituted 3H-indol-3-ols by the reaction of 2-isocyanophenyl ketones with Grignard reagents
449
Synthesis of 3-substituted 8,9-didehydroazepino[4,5-b]indolines via ring expansion reaction of pyrroloindolines
450
Synthesis of 3-substituted 8-hydroxy-3,4-dihydroisocoumarins via successive lateral and ortho-lithiations of 4,4-dimethyl-2-(o-tolyl)oxazoline
451
Synthesis of 3-Substituted and 2,3-Disubstituted-4H-1,4-Benzoxazines
452
Synthesis of 3-substituted and 3,4-disubstituted pyrazolin-5-ones
453
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
454
Synthesis of 3-substituted benzo[g]isoquinoline-5,10-diones: a convenient one-pot Sonogashira coupling/iminoannulation procedure
455
Synthesis of 3-substituted carbazole derivative as a host material for deep blue phosphorescent organic light-emitting diodes
456
Synthesis of 3-substituted imidazo[1,5-a]pyridines having 1-(N-picolinamidin-2-yl) group
457
Synthesis of 3-substituted indazoles and benzoisoxazoles via Pd-catalyzed cyclization reactions: application to the synthesis of nigellicine
458
Synthesis of 3-substituted Indoles through Yonemitsu Reaction with Copper Benzene-1,3,5-tricarboxylate acid Catalyst
459
Synthesis of 3-substituted isoindolin-1-ones via a palladium-catalysed 3-component carbonylation/amination/Michael addition process
460
Synthesis of 3-substituted-4-hydroxyquinoline N-oxides from the Baylis–Hillman adducts of o-nitrobenzaldehydes
461
Synthesis of 3-sulfanylpropanols containing three consecutive stereocenters via tandem Michael–aldol reaction of enoylthioamides with acetals as key reaction
462
Synthesis of 3-trialkylsilyl pyrazoles from β-oxo acylsilanes
463
Synthesis of 3-vinyl-2,5-dihydrofuran ring system via enyne metathesis
464
Synthesis of 3Y–ZrO2 nano-powders via a W/O emulsion
465
Synthesis of 3β-(5′-d-ribityl)cholestane, a putative biological precursor for fossil 3-alkylsteranes
466
Synthesis of 3β,6α-dihydroxy-5α-cholan-23-one
467
Synthesis of 3-β-d-ribofuranosyl-1 H-pyrazole-4-carboxamide
468
Synthesis of 3-β-d-ribofuranosylpyrazole-1-carboxamide
469
Synthesis of 4- and 6-substituted nitroindoles
470
Synthesis of 4-(1-oxo-isoindoline) and 4-(5,6-dimethoxy-1-oxo-isoindoline)-substituted phenoxypropanolamines and their β1-, β2-adrenergic receptor binding studies
471
Synthesis of 4-(2-arylvinyl)-8-hydroxyquinolines via anhydrous Heck coupling reaction and the PL properties of their Al complexes
472
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
473
Synthesis of 4-(2-hydroxyaryl)-3-nitro-4H-chromenes
474
Synthesis of 4-(2-Methylthiazol-4-yl)-Hexahydroquinoline and 1,4-Dihydropyrimidin Derivatives
475
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
476
Synthesis of 4(5)-phenylimidazole-based analogues of sphingosine-1-phosphate and FTY720: Discovery of potent S1P1 receptor agonists
477
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
478
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
479
Synthesis of 4-(cyclic dialkylamino)-7-azaindoles by microwave heating of 4-halo-7-azaindoles and cyclic secondary amines
480
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
481
Synthesis of 4-(thien-2-yl)-substituted coumarins through Lewis acid catalyzed Michael addition of thiophenes to 3-benzoylcoumarins followed by oxidation
482
Synthesis of 4-(trifluoromethyl) coumarins using nano sulfated-titania as solid acid catalyst under solvent-free conditions
483
Synthesis of 4-(trifluoromethyl)isoquinolines. Influence of trifluoromethyl group on the Pictet–Gams ring closure reaction
484
Synthesis of 4-, 5-, 6-, and 7-azidotryptamines
485
Synthesis of 4-, 8-, 12-arm star-branched polybutadienes with three different chain-end functionalities using a functionalized initiator
486
Synthesis of 4,17-diazasteroid inhibitors of human 5α-reductase Original Research Article
487
Synthesis of 4,4-(arylmethylene)bis(1H-pyrazol-5-ols) via multi-component reactions by using silica-bonded sulfamic acid derivatives
488
Synthesis of 4,4-(arylmethylene)bis(1H-pyrazol-5-ols) via multi-component reactions by using silica-bonded sulfamic acid derivatives
489
Synthesis of 4,4´-(arylmethylene)bis(1H-pyrazol-5-ols) catalyzed by nanosilica supported perchloric acid in water
490
Synthesis of 4,4΄-Diaminotriphenylmethane Derivatives Using H3PW12O40 and HZSM5 Zeolite under Solvent-Free Conditions
491
Synthesis of 4,4-bis(2-hydroperoxyalkyl)pyrazolidine-3,5-diones using manganese(III)-catalyzed autoxidation
492
Synthesis of 4,4-dialkoxy-3-piperidinols. Application to the synthesis of γ-acetate dehydropipecolinonitrile
493
Synthesis of 4,4-dimethyl-3,5-bis(diphenylphosphino)cyclohexanone
494
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
495
Synthesis of 4,5-diaryl-1,2,3-benzenetricarboxylates by reaction of 4-hydroxycyclopent-2-en-1-one-2-carboxylates with dimethyl acetylenedicarboxylate
496
Synthesis of 4,5-diarylquinazolines: a system with cofacial aromatic rings. Diazines. Part 39
497
Synthesis of 4,5-difluoroimidazole
498
Synthesis of 4,5-disubstituted-3-trihalomethylisothiazoles
499
Synthesis of 4,5-fused tricyclic quinolines via an acid-promoted intramolecular Friedel–Crafts allenylation of aniline derivatives
500
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
501
Synthesis of 4,6-diamino-5-(polyhydroxyalkylamido)pyrimidines: conformation of the sugar chain
502
Synthesis of 4,6-dimethyl-tetrahydro- and hexahydro-dibenzothiophene
503
Synthesis of 4,6-disubstituted pyrimidines via Suzuki and Kumada coupling reaction of 4,6-dichloropyrimidine
504
Synthesis of 4,7-indoloquinones from indole-7-carbaldehydes by Dakin oxidation
505
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
506
Synthesis of 4,8-Diarylcinnolines and Quinazolines with Potential Applications in Nonlinear Optics. Diazines. Part 28
507
Synthesis of 4-[N-methyl-4-pyridinio]-phenolate (POMP) and negative solvatochromism of this model molecule in view of nonlinear optical applications
508
Synthesis of 4′,4′-C-diaminomethyl nucleoside derivative as a building block for constructing libraries via amide bond formation
509
Synthesis of 4′-aryl-2′,3′-dideoxynucleoside analogues
510
Synthesis of 4′-benzoyloxycordycepin from adenosine
511
Synthesis of 4′-C, 3′-O bicyclic thymidine analogues using ring closure metathesis
512
Synthesis of 4′-epi-iodo-4′-deoxy-daunorubicin, a potential cancer radiotherapeutic agent
513
Synthesis of 4′-fluoroadenosine as an inhibitor of S-adenosyl-L-homocysteine hydrolase
514
Synthesis of 4′-modified noraristeromycins to clarify the effect of the 4′-hydroxyl groups for inhibitory activity against S-adenosyl-l-homocysteine hydrolase
515
Synthesis of 4′-O-acetyl-maltose and α-d-galactopyranosyl-(1→4)-d-glucopyranose for biochemical studies of amylose biosynthesis Original Research Article
516
Synthesis of 4′-substituted 2,2′:6′,2″-terpyridines via a Mitsunobu reaction
517
Synthesis of 4′-thionucleosides by 1,3-dipolar cycloadditions of the simplest thiocarbonyl ylide with alkenes bearing electron-withdrawing groups
518
Synthesis of 4″-alkoxy avermectin derivatives using rhodium carbenoid-mediated O–H insertion reaction
519
Synthesis of 45S5 Bioglass® via a straightforward organic, nitrate-free sol–gel process
520
Synthesis of 4A zeolites from kaolin for obtaining 5A zeolites through ionic exchange for adsorption of arsenic
521
Synthesis of 4-acylpyrazolone Schiff base ligand grafted silica and selectivity in adsorption of lanthanides from aqueous solutions
522
Synthesis of 4-alkoxy-2-phenylquinoline derivatives as potent antiplatelet agents
523
Synthesis of 4-alkoxy-4-methyl- and 4-alkoxy-4-fluoromethyl-1,3-benzoxazinones
524
Synthesis of 4-alkoxycarbonyl-butenolides by uncatalyzed one-pot cyclization of 1,3-bis(silyloxy)alk-1-enes with oxalyl chloride
525
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
526
Synthesis of 4-alkyl-3-bromo-2(5H)-furanones and unsymmetrically disubstituted 3,4-dialkyl-2(5H)-furanones by palladium-catalyzed cross-coupling reactions
527
Synthesis of 4-alkyl-pyrrolidine-3-carboxylic acid stereoisomers
528
Synthesis of 4-allenyl and 4-proparyl-2-azetidinone via Zn-mediated Barbier-type reaction and Pt-catalyzed intramolecular amidation to carbapenem skeletons
529
Synthesis of 4-allylquinazolines from N-(2-cyanoaryl)amides via the In-mediated allylation of nitrile and dehydrative cyclization cascade
530
Synthesis of 4-amino-1,2,3,4-tetrahydropyridine derivatives by intramolecular nucleophilic addition of tertiary enamides to in-situ generated imines
531
Synthesis of 4-amino-3-oxo-tetrahydroazepino[3,4-b]indoles: new conformationally constrained Trp analogs
532
Synthesis of 4-amino-4,5-dideoxy-l-lyxofuranose derivatives and their evaluation as fucosidase inhibitors Original Research Article
533
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
534
Synthesis of 4-aminoguaiazulene and its δ-lactam derivatives
535
Synthesis of 4-anilinopiperidine methyl esters, intermediates in the production of carfentanil, sufentanil, and remifentanil
536
Synthesis of 4-arms hydroxy-functionalized PMMA-b-PE through combining free radical polymerization with coordination polymerization
537
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
538
Synthesis of 4-aryl-2,3-dihydropyrroles via Rh-catalyzed intramolecular hydroamino-methylation reaction
539
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
540
Synthesis of 4-Aryl-4H-Chromene Derivatives with Boric Acid: Evaluation of Their in vitro Anti-Angiogenesis Effects and Possible Mechanism of Action
541
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
542
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
543
Synthesis of 4-aryl-6-indolylpyridine-3-carbonitriles and evaluation of their antiproliferative activity
544
Synthesis of 4-Arylaminoquinazolines and 2-Aryl-4-arylaminoquinazolines from 2-Aminobenzonitrile, Anilines and Formic Acid or Benzaldehydes
545
Synthesis of 4-aryl-azetidinones via intramolecular alkylation of nucleophilic arenes using acyliminium cations
546
Synthesis of 4-arylidenecyclohexane-1,3-diones from the Baylis–Hillman acetates
547
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
548
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
549
Synthesis of 4-azacyclopent-2-enones and 5,5-dialkyl-4-azacyclopent-2-enones
550
Synthesis of 4-azepanones and heteroaromatic-fused azepines
551
Synthesis of 4-aziridino[C60]fullerene-1,8-naphthalimide (C60-NI dyads) and their photophysical properties
552
Synthesis of 4-Azo-3,5-Substituted-1,2,4-Triazole Polymers and Study of their Applications
553
Synthesis of 4b,5,10a,11-tetrahydroindeno[1,2-b]quinolin-10-ones from Baylis–Hillman adducts
554
Synthesis of 4-benzyl-3-phenylbutenolide natural products
555
Synthesis of 4-butyl-1-substituted-4H-[1,2,4]triazolo[4,3-a]quinazolin-5-ones as new class of H1-antihistaminic agents
556
Synthesis of 4-carboxy-4-pyridylpiperidines through palladium-catalyzed α-arylation of esters
557
Synthesis of 4-cyano and 4-nitrophenyl 1,6-dithio-d-manno-, l-ido- and d-glucoseptanosides possessing antithrombotic activity Original Research Article
558
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
559
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
560
Synthesis of 4-cyanophenyl 2-azido-2-deoxy- and 3-azido-3-deoxy-1,5-dithio-β-d-xylopyranosides
561
Synthesis of 4-cyanophenyl 2-deoxy-1,5-dithio-β-d-threo-pentopyranoside
562
Synthesis of 4-cyanophenyl 4-azido-4-deoxy-1,5-dithio-β-d-xylopyranoside
563
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
564
Synthesis of 4-cyanophenyl and 4-nitrophenyl 1,5-dithio-l- and -d-arabinopyranosides possessing antithrombotic activity
565
Synthesis of 4-cyanophenyl and 4-nitrophenyl 2-azido-2-deoxy-1,5-dithio-β-d-arabino- and -β-d-lyxopyranosides possessing antithrombotic activity
566
Synthesis of 4-demethoxyadriamycinone utilizing ruthenium-catalyzed oxidation of allyl acetates
567
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
568
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
569
Synthesis of 4-dialkylaminopyridine derivatives through ring-rearrangement of 3-nitro-2H-pyran-2-one acetamidines
570
Synthesis of 4-Diphosphocytidyl-2-C-Methyl-D-Erythritol 2-Phosphate and Kinetic Studies of Mycobacterium tuberculosis IspF
571
Synthesis of 4-epi-2-deoxy-2-Heq-N-acetylneuraminic acid and 2,4-dideoxy-2-Heq N-acetylneuraminic acid
572
Synthesis of 4-fluoroalkyl-substituted pyridazines from fluorinated diazodiketones
573
Synthesis of 4-functionalized aryl-3,5-diacyl-1,4-dihydropyridines
574
Synthesis of 4-functionalized terdendate pyridine-based ligands
575
Synthesis of 4H-[1,3]dithiolo[4,5-b]pyrroles through the reaction of benzoyl isothiocyanate and dialkyl acetylenedicarboxylates in the presence of Ph3P
576
Synthesis of 4-halophosphaisocoumarins via halocyclization of 2-(1-alkynyl)phenylphosphonates
577
Synthesis of 4-haloserotonin derivatives and synthesis of the toad alkaloid dehydrobufotenine
578
Synthesis of 4H-benzo[e]-1,2-selanazin-4-one derivatives: a new heterocyclic ring system
579
Synthesis of 4H-pyrano[2,3-d]pyrimidine derivatives under solvent-free conditions
580
Synthesis of 4H-pyrans catalyzed by thermol-regulated PEG1000-based ionic liquid/EM
581
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
582
Synthesis of 4-hydroxy-1-methylindole and benzo[b]thiophen-4-ol based unnatural flavonoids as new class of antimicrobial agents Original Research Article
583
Synthesis of 4-hydroxy-3-[(E)-2-(6-substituted-9H-purin-9-yl)vinyl]coumarins as lipoxygenase inhibitors
584
Synthesis of 4-hydroxy-7-dimethylamino-3-pyrazolinylcoumarins and their polarity-sensitive properties
585
Synthesis of 4-hydroxyderricin and related derivatives
586
Synthesis of 4-hydroxymethyl-2,4-methanoproline
587
Synthesis of 4-hydroxysphinganine and characterization of sphinganine hydroxylase activity in corn
588
Synthesis of 4-Methoxy-1, 3-Benzenediolylhydrazones and Evaluation of Their Anti-Platelet Aggregation Activity
589
Synthesis of 4-methoxy-1H-phenalen-1-one: a subunit related to natural phenalenone-type compounds
590
Synthesis of 4-methoxy-3,5-dinitrobenzaldehyde: a correction to supposed tele nucleophilic aromatic substitution
591
Synthesis of 4-methylcoumarin-7-yl β-d-galactofuranoside, a fluorogenic substrate for galactofuranosidase
592
Synthesis of 4-methyl-thio-phenyl-propylamine and the evaluation of its interaction with different amine oxidases Original Research Article
593
Synthesis of 4-methylumbelliferyl-β-d-glucan oligosaccharides as specific chromophoric substrates of (1 → 3),(1 → 4)-β-d-glucan 4-glucanohydrolases
594
Synthesis of 4-monofluoromethylenyl- and cis-4-monofluoromethyl-l-pyroglutamic acids via a novel dehydrofluorination
595
Synthesis of 4-N-alkyl and ribose-modified AICAR analogues on solid support
596
Synthesis of 4-nitromethylene-1,4-dihydropyrimidine derivatives as pyrimidine nucleoside analogues
597
Synthesis of 4-Nitrophenyl Sulfones and Application in the Modified Julia Olefination
598
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
599
Synthesis of 4-O- and 6-O-(2′-iodoethyl)-d-glucose
600
Synthesis of 4-O-[3-(aryl)prop-2-ynyl]-Neu5Ac2en and its 4-epi-analogs modified at C-4 by Sonogashira coupling reaction
601
Synthesis of 4-O-d-Mannopyranosyl-α-d-glucopyranosides by Intramolecular Glycosylation of 6-O-Tethered Mannosyl Donors
602
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
603
Synthesis of 4-O-glycosylated 1-deoxynojirimycin derivatives as disaccharide mimics-based inhibitors of human β-glucocerebrosidase
604
Synthesis of 4-oxepanones by the Lewis acid-promoted ring-expansion reaction of cyclopropapyranones
605
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
606
Synthesis of 4-oxo-4,7-dihydrofuro[2,3-b]pyridine-5-carboxamides with broad-spectrum human herpesvirus polymerase inhibition
607
Synthesis of 4-pentenoic and 5-hexenoic acids on polystyrene resin and their use as cleavable linkers
608
Synthesis of 4-phenoxybenzamide adenine dinucleotide as NAD analogue with inhibitory activity against enoyl-ACP reductase (InhA) of Mycobacterium tuberculosis
609
Synthesis of 4-Phenyl-4,5-dihydropyranopyrazolone Derivatives with Activated Potassium Carbonate: Evaluation of Anticancer Activity on Cancer Cell Lines and Apoptosis Mechanism
610
Synthesis of 4-phenylpyrrolidin-2-one via dynamic kinetic resolution catalyzed by ω-transaminases
611
Synthesis of 4-phosphono-β-lactams via phosphite addition to acyliminium salts
612
Synthesis of 4-Pyrazolylmethylidene-2-Oxazoline and -2-Imidazoline Derivatives
613
Synthesis of 4-pyrido-6-aryl-2-substituted amino pyrimidines as a new class of antimalarial agents Original Research Article
614
Synthesis of 4-substituted 3-(indol-3-yl)maleimides and azepines with annelated indole and maleimide nuclei
615
Synthesis of 4-substituted 4-arylpiperidines
616
Synthesis of 4-substituted and 3,4-disubstituted indazole derivatives by palladium-mediated cross-coupling reactions
617
Synthesis of 4-substituted azepino[3,4-b]indole-1,5-diones
618
Synthesis of 4-substituted homoallylic alcohols via a one-pot tandem Lewis-acid catalyzed crotylboration-[3,3]-sigmatropic rearrangement
619
Synthesis of 4-substituted phenyl 2,5-anhydro-1,6-dithio-α-d-gluco- and -α-l-guloseptanosides possessing antithrombotic activity Original Research Article
620
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
621
Synthesis of 4-Substituted Phosphacoumarins via Cross-Coupling of 4-Tosylphosphacoumarins with Organozinc Reagents
622
Synthesis of 4-substituted pyrano[4,3-b]pyran-2,5-diones in an ionic liquid
623
Synthesis of 4-substituted tetrahydropyridines by cross-coupling of enol phosphates
624
Synthesis of 4-substituted-2-acetamido-2,4-dideoxy-mannopyranoses using 1,6-anhydro sugar chemistry
625
Synthesis of 4-sulfonatooxy-2,2,6,6-tetramethylpiperidine-1-yloxyl derivatives for investigation of ionic liquids
626
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
627
Synthesis of 4-thiofuranoid 1,2-glycals and their application to stereoselective synthesis of 4′-thionucleosides
628
Synthesis of 4-thiophen-2′-yl-1,4-dihydropyridines as potentiators of the CFTR chloride channel Original Research Article
629
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
630
Synthesis of 4-trifluoromethylpyrido[1,2-a]pyrimidin-2-ones utilizing activated alkynoates
631
Synthesis of 4-trifluoromethylsteroids: A novel class of steroid 5α-reductase inhibitors
632
Synthesis of 4-trimethylammonio-2,2,6,6-tetramethylpiperidine-1-yloxyl with various anions for investigation of ionic liquids
633
Synthesis of 4-unsubstituted 2H-1,2,3-benzothiadiazine 1,1-dioxides via ortho lithiation of protected benzaldehyde derivatives
634
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
635
Synthesis of 4-unsubstituted dihydropyrimidines. Nucleophilic substitution at position-2 of dihydropyrimidines
636
Synthesis of 5- and 6-(6-Chloro-3-pyridyl)-2-azabicyclo[2.2.0]hexanes. Epibatidine Analogs
637
Synthesis of 5-(1-H or 1-alkyl-5-oxopyrrolidin-3-yl)-8-hydroxy-[1,6]-naphthyridine-7-carboxamide inhibitors of HIV-1 integrase
638
Synthesis of 5(20)deoxydocetaxel, a new active docetaxel analogue
639
Synthesis of 5-(2-amino-2-deoxy-β- -glucopyranosyloxymethyl)-2′-deoxyuridine and its incorporation into oligothymidylates
640
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
641
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
642
Synthesis of 5-(3-indolyl)oxazole natural products. Structure revision of Almazole D
643
Synthesis of 5(6)-dihydro-OSW-1 by using the intact skeleton of tigogenin
644
Synthesis of 5-(7′-indolyl)oxazoles and 2,5-di-(7′-indolyl)oxazoles
645
Synthesis of 5-(7-hydroxyhept-3-enyl)-1,2-dithiolan-3-one 1-oxide, a core functionality of antibiotic leinamycin
646
Synthesis of 5-(mercaptomethyl)-3(E)-undecene-1,11-dioic acid, a non-peptide glutathione analog
647
Synthesis of 5-(perfluoroalkylmethyl)-1,3-dioxolan-4-ones
648
Synthesis of 5-(phenylsulfanyl)-1,4-dihydropyrazine-2,3-diones via an unexpected microwave-assisted cascade reaction
649
Synthesis of 5-(sulfamoylmethyl)indoles
650
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
651
Synthesis of 5-(trifluoromethyl)cyclohexane-1,3-dione and 3-amino-5-(trifluoromethyl)cyclohex-2-en-1-one: new trifluoromethyl building block
652
Synthesis of 5-(ω-sulfhydrylalkyl)salicylaldehydes as precursors for the preparation of alkanethiol-modified metal salens
653
Synthesis of 5,10,15,20-tetrakis(2-amino-5-methoxyphenyl)-porphyrin: a versatile building block for porphyrin face selection
654
Synthesis of 5,10-diphenylporphyrin
655
Synthesis of 5,15-diarylporphyrins via orthoesters condensation with aryldipyrromethanes
656
Synthesis of 5,5,6,6,21,21,22,22-octamethyl-5,6,21,22-tetragerma[10.10]paracyclophane
657
Synthesis of 5,5′-bis-benzofurans and 5-arylbenzofurans
658
Synthesis of 5,5′-diarylated 2,2′-bithiophenes via palladium-catalyzed arylation reactions
659
Synthesis of 5,6-bis(alkyn-1-yl)pyrimidines and related nucleosides
660
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
661
Synthesis of 5,6-dihydro-2H-thiins and 2,3-dihydro-1,4-oxathiins based on 1-benzylsulfonyl-1,1-dihydropolyfluoroalkan-2-ones
662
Synthesis of 5,6-dihydro-4H-1,3-thiazine containing peptide mimics from N-(3-hydroxypropyl)thioamides and epimerization studies
663
Synthesis of 5,6-dihydro-4-hydroxy-2-pyrones via formal cycloaddition reactions
664
Synthesis of 5,6-dihydrobenz[c]acridines: a comparative study
665
Synthesis of 5,6-dihydrophenanthridines via N,O-acetal TMS ethers
666
Synthesis of 5,7,12,14-Tetraarylpentacenes from Pentacene-5,7,12,14-tetrone and Characterisation of the Tetrol Intermediates
667
Synthesis of 5,8-dimethoxy-3-hydroxy-4-quinolone, a reported inhibitor of HIV RT, and evidence the original proposed structure was incorrect
668
Synthesis of 5′,9-anhydro-3-(β-d-ribofuranosyl)xanthine, and 3,5′-anhydro-xanthosine as potential anti-hepatitis C virus agents
669
Synthesis of 5′-C-methyl-1′,3′-dioxolan-4′-yl nucleosides
670
Synthesis of 5′-functionalized adenosine: suppression of cyclonucleoside formation
671
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
672
Synthesis of 5′-seleno-xylofuranosides
673
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
674
Synthesis of 5″-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca2+-mobilizing agent: The first antagonists modified at the N1-ribose moiety
675
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
676
Synthesis of 5-Acetoxy-2(5H)-Furanones through Manganese(III)-Promoted Functionalization of Arylacetylenes
677
Synthesis of 5-acetyl-2-aminopyrrole C-deoxyribonucleoside
678
Synthesis of 5-alkoxymethyl- and 5-aminomethyl-substituted 8-hydroxyquinoline derivatives and their luminescent Al(III) complexes for OLED applications
679
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
680
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
681
Synthesis of 5-alkyl-4-amino-2-(trifluoromethyl)pyridines and their transformation into trifluoromethylated 1H-pyrazolo[4,3-c]pyridines
682
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
683
Synthesis of 5-alkylidene-2,5-dihydropyrrol-2-ones based on cyclizations of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with oxalyl chloride
684
Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles
685
Synthesis of 5-alkynylated uracil–morpholino monomers using Sonogashira coupling
686
Synthesis of 5-amino-1-aryl-4-cyanoimidazoles from formamidines under solvent-free condition
687
Synthesis of 5-amino-2-aminoalkyl-1,3-oxazol-4-ylphosphonic acid derivatives and their use in the preparation of phosphorylated peptidomimetics
688
Synthesis of 5-amino-2-selenoxo-1,3-imidazole-4-carboselenoamides by the reaction of isoselenocyanates with aminoacetonitriles
689
Synthesis of 5-aminoisoxazolines from N-allyl compounds and nitrile oxides via tandem isomerization-1,3-dipolar cycloaddition
690
Synthesis of 5-aminothiazoles as building blocks for library synthesis
691
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
692
Synthesis of 5-aryl-5′-formyl-2,2′-bithiophenes as new precursors for nonlinear optical (NLO) materials
693
Synthesis of 5-arylamino-1-arylpyrazoles from 5-aminopyrazoles with arylhalides via CuI catalyzed Ullman coupling reaction
694
Synthesis of 5-arylhistidines via a Suzuki–Miyaura cross-coupling
695
Synthesis of 5-arylidene-2-amino-4-azolones and evaluation of their anticancer activity Original Research Article
696
Synthesis of 5-arylidene-2-aryl-3-(2-chlorophenothiazinoacetamidyl)l,3-thiazolidin-4-ones as antifungal and anticonvulsant agents
697
Synthesis of 5-arylmethylene-pyrimidine-2,4,6-trione and 2-arylidenemalononitriles derivatives using a new Brønsted acid nano magnetic catalyst
698
Synthesis of 5-arylpyrrolo[2,1-c][1,4]benzodiazepines under mild cyclodehydration conditions
699
Synthesis of 5-arylthiazoles. Comparative study between Suzuki cross-coupling reaction and direct arylation
700
Synthesis of 5-aryltriazole ribonucleosides via Suzuki coupling and promoted by microwave irradiation
701
Synthesis of 5-aza-analogues of angucyclines: manipulation of the 2-deoxy-C-glycoside subunit
702
Synthesis of 5-benzoylacenaphthene in the presence of Lewis acidic ionic liquids
703
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
704
Synthesis of 5-bromo-6-methyl imidazopyrazine, 5-bromo and 5-chloro-6-methyl imidazopyridine using electron density surface maps to guide synthetic strategy
705
Synthesis of 5-chloro-N-aryl-1H-indole-2-carboxamide derivatives as inhibitors of human liver glycogen phosphorylase a Original Research Article
706
Synthesis of 5-deazaflavin derivatives and their activation of p53 in cells Original Research Article
707
Synthesis of 5-deazathiogirollines: analogs of a natural antitumor agent
708
Synthesis of 5-deoxy-5-epifluoro derivatives of arbekacin, amikacin, and 1-N-[(S)-4-amino-2-hydroxybutanoyl]tobramycin (study on structure — toxicity relationships)
709
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
710
Synthesis of 5-deoxypterocarpens, pterocarpens, and coumestans by intramolecular Heck reaction
711
Synthesis of 5-deoxy-β-d-galactofuranosides as tools for the characterization of β-d-galactofuranosidases Original Research Article
712
Synthesis of 5-endo-, 5-exo-, 6-endo- and 6-exo-hydroxylated analogues of epibatidine
713
Synthesis of 5-epiaragusterol A
714
Synthesis of 5-ethoxymethylfurfural from 5-hydroxymethylfurfural and fructose in ethanol catalyzed by MCM-41 supported phosphotungstic acid
715
Synthesis of 5-Fluorouracil nanoparticles via supercritical gas antisolvent process
716
Synthesis of 5-fluorouridine 5′-diphosphate galactose from 5-fluorouridine by chemical phosphorylation and microbial uridylyl transfer
717
Synthesis of 5-fluorovinyl derivatives of pyrimidines via Suzuki–Miyaura coupling and their 1,3-dipolar cycloaddition reactions with nitrones
718
Synthesis of 5-haloethynyl- and 5-(1,2-dihalo)vinyluracil nucleosides: Antiviral activity and cellular toxicity Original Research Article
719
Synthesis of 5-halogenated 1,2,3-triazoles under stoichiometric Cu(I)-mediated azide–alkyne cycloaddition (CuAAC or ‘Click Chemistry’) Original Research Article
720
Synthesis of 5-heteroarylazulenes: first selective electrophilic substitution at the 5-position of azulene
721
Synthesis of 5H-pyridazino[4,5-b]indoles and their benzofurane analogues utilizing an intramolecular Heck-type reaction
722
Synthesis of 5-HT3 receptor antagonists, [11C]Y-25130 and [11C]YM060
723
Synthesis of 5-Hydroxy- and 5-Amino-1-tosyl-5-phenyl-3-(2-arylvinyl)4,5-dihydropyrazoles
724
Synthesis of 5-hydroxy-2-(β-d-ribofuranosyl)pyran-4-one from a pyranulose glycoside
725
Synthesis of 5-hydroxyquinolines
726
Synthesis of 5-membered heterocycles using benzoylacetonitriles as synthon
727
Synthesis of 5-methoxylated 3-pyrrolin-2-ones via the rearrangement of chlorinated pyrrolidin-2-ones
728
Synthesis of 5-methylfuro[3,2-c]quinolin-4(5H)-one via palladium-catalysed cyclisation of N-(2-iodophenyl)-N-methyl-3-furamide
729
Synthesis of 5-nitro- and 5-aminobenzimidazolone-2
730
Synthesis of 5-O-methylembelin
731
Synthesis of 5-substituted 1H-tetrazoles catalyzed by ceric ammonium nitrate supported HY-zeolite
732
Synthesis of 5-substituted 1H-tetrazoles catalyzed by ytterbium triflate hydrate
733
Synthesis of 5-substituted 2-(4- or 3-methoxyphenyl)-4(1H)-quinolones
734
Synthesis of 5-substituted 2,3-dihydrobenzofurans in a one-pot oxidation/cyclization reaction
735
Synthesis of 5-substituted 3-mercapto-1,2,4-triazoles via Suzuki–Miyaura reaction
736
Synthesis of 5-substituted analogues of huperzine A
737
Synthesis of 5-substituted derivatives of isophthalic acid as non-polymeric amphiphilic coating for metal oxide nanoparticles
738
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
739
Synthesis of 5-substituted pipecolic acid derivatives as new conformationally constrained ornithine and arginine analogues
740
Synthesis of 5-substituted quinazolinone derivatives and their inhibitory activity in vitro
741
Synthesis of 5-Substituted-1,3,4-Oxadiazole-2(3H)-Thiones Under Microwave Irradiation
742
Synthesis of 5-substituted-3,4-dihydroxycyanopyrrolidines. An easy access to polyhydroxyprolines
743
Synthesis of 5-thio-l-altrose
744
Synthesis of 5-Thiomannose-containing oligomannoside mimics: Binding abilities to concanavalin A
745
Synthesis of 5-thioxo-6H-imidazo[1,2-c]quinazolines and related compounds based on cyclocondensations of 2-isothiocyanatobenzonitrile (ITCB) with α-aminoketones
746
Synthesis of 5-trichloromethyl-Δ4-1,2,4-oxadiazolines and their rearrangement into formamidine derivatives
747
Synthesis of 6- and 7-propargyloxy derivatives of 4-(3-fluoroanilino)-quinazoline
748
Synthesis of 6- or 4-functionalized indoles via a reductive cyclization approach and evaluation as aromatase inhibitors
749
Synthesis of 6-(2-thienyl)purine nucleoside derivatives that form unnatural base pairs with pyridin-2-one nucleosides
750
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
751
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)
752
Synthesis of 6(α,β)-aminocholestanols as ergosterol biosynthesis inhibitors
753
Synthesis of 6-, 7- and 8-membered cyclosiloxanes having multifunctional groups
754
Synthesis of 6-, 7-, and 8-membered lactones via the nickel-catalysed electrochemical arylation of electron-deficient olefins
755
Synthesis of 6,6-bisbenzannulated spiroketals related to the rubromycins using a double intramolecular hetero-Michael addition (DIHMA)
756
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
757
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
758
Synthesis of 6,7-diaza-19-norvitamin D compounds
759
Synthesis of 6,7-dichloropyrido[1,2-a]benzimidazole-8,9-dione and its analogues and their reactions with nucleophiles
760
Synthesis of 6,7-dideoxy-7-isothiocyanatoheptoses: stable fully unprotected monosaccharide isothiocyanates
761
Synthesis of 6,7-dihydro-5H-dibenzo[c,e]azepines and biaryls by palladium-catalyzed Ullmann reaction
762
Synthesis of 6,7-disubstituted-5H-pyrrolo[2,3-b]pyrazines via palladium-catalyzed heteroannulation
763
Synthesis of 6,7-ethylenedioxyquinoxalines and pyrido[2,3-b]pyrazines as intermediates in the preparation of antineoplastic agents
764
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
765
Synthesis of 6′-acylamido-6′-deoxy-α-d-galactoglycerolipids Original Research Article
766
Synthesis of 6′-deoxy-6′-fluorosucrose Original Research Article
767
Synthesis of 6′-GM2, a regioisomer of ganglioside GM2, for studying the mechanism of action of GM2 activator
768
Synthesis of 60- and 72 kDa heat shock proteins in early porcine embryogenesis
769
Synthesis of 61-bis(1-adamantylcarbamoyl)-1,2-methano[60]fullerene and its antagonistic effect on haloperidol-induced catalepsy in mice
770
Synthesis of 6-acyl-5,8-quinolinediols by photo-Friedel–Crafts acylation using sunlight
771
Synthesis of 6-Acylmethylphenanthridine Enaminones
772
Synthesis of 6a-hydroxypterocarpans via intramolecular benzoin condensation
773
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
774
Synthesis of 6-amino-1,6-anhydro-6-deoxysugar derivatives
775
Synthesis of 6-Amino-1H-Indole-4,7- Quinones
776
Synthesis of 6-amino-6-deoxyhyaluronan as an intermediate for conjugation with carboxylate-containing compounds: application to hyaluronan–camptothecin conjugates Original Research Article
777
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
778
Synthesis of 6-aryl-2,4-diamino-pyrimidines and triazines using palladium catalysed Suzuki cross-coupling reactions
779
Synthesis of 6-aryl-2′-deoxyuridine nucleosides via a Liebeskind cross-coupling methodology
780
Synthesis of 6-aryluridines via Suzuki–Miyaura cross-coupling reaction at room temperature under aerobic ligand-free conditions in neat water
781
Synthesis of 6-Aziridineyl and 6-Triazol-yl of D- Glucitol Derivatives
782
Synthesis of 6-bromo-2-arylindoles using 2-iodobenzoic acid as precursor
783
Synthesis of 6-carboxylated phenanthridines by oxidative alkoxycarbonylation–cyclization of 2-isocyanobiphenyls with carbazates
784
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
785
Synthesis of 6-cyano and 6-unsubstituted 2-aryl-8-oxopurine from a common 2-oxoimidazole precursor
786
Synthesis of 6-deoxy-5-thio-d-glucose
787
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
788
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
789
Synthesis of 6-deoxy-6-halolaminarans and conversion of 6-chloro-6-deoxylaminaran into the 6-amino-6-deoxy derivative
790
Synthesis of 6-deoxy-l-idose and l-acovenose from 1,2:5,6-di-O-isopropylidene-α-d-glucofuranose Original Research Article
791
Synthesis of 6-deoxy-N-Cbz-d,l-iminoglycal-derived vinyl epoxides and examination of their regio- and stereoselectivity in nucleophilic addition reactions
792
Synthesis of 6-ethynylpurine derivatives
793
Synthesis of 6-formyl-pyridine-2-carboxylate derivatives and their telomerase inhibitory activities
794
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
795
Synthesis of 6H-benzo[c]chromen-6-ones by cyclocondensation of 1,3-dicarbonyl compounds with 4-chloro-3-formylcoumarin
796
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
797
Synthesis of 6H-naphtho[2,3-c]chromene-7,12-diones via palladium-catalyzed intramolecular cyclization of 2-bromo-3-aryloxymethyl-1,4-naphthoquinones
798
Synthesis of 6-hydroxy-2-naphthoic acid from 2,6-diisopropylnaphthalene using NHPI as a key catalyst
799
Synthesis of 6-hydroxymethyl-5,6-dihydro-4H-1,2-oxazines by one-pot-cyclization of dilithiated oximes with epibromohydrin
800
Synthesis of 6I-amino-6I-deoxy-2I–VII,3I–VII-tetradeca-O-methyl-cyclomaltoheptaose
801
Synthesis of 6-imino-5-tetrahydro-1H-2-pyrrolylidenhexahydro-2,4-pyrimidinediones as intermediates for the synthesis of C-azanucleosides
802
Synthesis of 6-methoxy-4H-1-benzopyran-7-ol, a character donating component of the fragrance of Wisteria sinensis
803
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
804
Synthesis of 6-N-(benzothiazol-2-yl)deoxyadenosine and its exciton-coupled circular dichroism Original Research Article
805
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
806
Synthesis of 6-O-methotrexylhyaluronan as a drug delivery system Original Research Article
807
Synthesis of 6-O-methyl-azithromycin and its ketolide analogue via Beckmann rearrangement of 9(E)-6-O-methyl-erythromycin oxime
808
Synthesis of 6-oxacyclopropa[a]indene derivatives starting from Baylis–Hillman adducts via Pd-mediated C(sp3)–H activation
809
Synthesis of 6-phenyl-2,2′-bipyridine ligands bearing polyaromatic substituents
810
Synthesis of 6-substituted 1-phenylbenzazepines and their dopamine D1 receptor activities Original Research Article
811
Synthesis of 6-substituted 5-cyano-7-hydroxy-2-carboxybenzofurans
812
Synthesis of 6-substituted 7-aryl-5,6-dihydropyrido[2,3-d]pyrimidine(1H,3H)-2,4-diones using the Vilsmeier reaction
813
Synthesis of 6-substituted imidazo[2,1-b]thiazoles via Pd/Cu-mediated Sonogashira coupling in water
814
Synthesis of 6-substituted tetrahydropyridinones and cyclization to indolizidine and quinolizidine structures
815
Synthesis of 6-sulfodisaccharides by beta-N-acetylhexosaminidase-catalyzed transglycosylation
816
Synthesis of 6-thio pseudo glycolipids and their orientation on a gold slide studied by IRRAS
817
Synthesis of 6-vinyl and 5-vinylproline analogues of ascomycin
818
Synthesis of 6Z,8E-heneicosadien-11-one, a sex pheromone of the painted apple moth, Teia anartoides
819
Synthesis of 7- and 10-spermine conjugates of paclitaxel and 10-deacetyl-paclitaxel as potential prodrugs
820
Synthesis of 7-(E)-alkenyl-4-amino-3-quinolinecarbonitriles via Pd-mediated Heck, Stille, and Suzuki reactions
821
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
822
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
823
Synthesis of 7,8-disubstituted benzolactam-V8 and its binding to protein kinase C
824
Synthesis of 7,9-dideoxybaccatin IV analogs from sinenxan A
825
Synthesis of 7′-[123I]iodo-d-luciferin for in vivo studies of firefly luciferase gene expression
826
Synthesis of 7-alkoxy-4-trifluoromethylcoumarins via the von Pechmann reaction catalyzed by molecular iodine
827
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
828
Synthesis of 7-aryl-1,8-naphthyridines via addition of aryl boronic acids to 1,8-naphthyridine N-oxides
829
Synthesis of 7-azabicyclo[2.2.1]heptane derivatives via bridgehead radicals
830
Synthesis of 7-azabicyclo[2.2.1]heptane-1,4-dicarboxylic acid, a rigid non-chiral analogue of 2-aminoadipic acid
831
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
832
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
833
Synthesis of 7-chloro-4-substituted aminoquinolines and their in vitro ability to produce methemoglobin in canine hemolysate
834
Synthesis of 7-cyano- and 7-acetamido-indoles via cyanocarbonation/hydrogenation of 7-formyl indole
835
Synthesis of 7-cycloalkylimino substituted 3-amino-6-fluoro-2-methyl-3H-quinazolin-4-ones
836
Synthesis of 7-deoxycholic amides or cholanes containing distinctive ion-recognizing groups at C3 and C12 and evaluation for ion-selective ionophores
837
Synthesis of 7-hydroxy-4-methylcoumarin via the Pechmann reaction with Amberlyst ion-exchange resins as catalysts
838
Synthesis of 7-hydroxycoumarins by Pechmann reaction using Nafion resin/silica nanocomposites as catalysts
839
Synthesis of 7-membered cyclic hydroxyguanidines: Novel HIV-1 protease inhibitors
840
Synthesis of 7-methoxybenzolactam-V8 using aminomercuration as a key reaction
841
Synthesis of 7-O-(2-deoxy-2-sulfamido-α-d-glucopyranosyl)-4-methylcoumarin sodium salt: a fluorogenic substrate for sulfamidase
842
Synthesis of 7-O-galloyl-d-sedoheptulose
843
Synthesis of 7-oxa-phomopsolide E and its C-4 epimer
844
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
845
Synthesis of 7-Substituted Fluoroquinolone Derivatives Contain- ing Triazolidine Dione Moiety and In Vitro Evaluation of Their Cytotoxic Effects
846
Synthesis of 7-thiaarachidonic acid as a mechanistic probe of prostaglandin H synthase-2
847
Synthesis of 7-trifluoromethylpyrazolo[1,5-a]pyridinedicarboxylate
848
Synthesis of 7α- and 7β-spermidinylcholesterol, squalamine analogues
849
Synthesis of 7α-methoxy-2-(1,3-dithiolan-2-ylidene)cephem sulphones. A new series of human leukocyte elastase inhibitors
850
Synthesis of 7α-substituted androstenediones by a 1,4-conjugate addition approach
851
Synthesis of 8-(2′-deoxy-β-d-ribofuranosyl)imidazo[1,2-a]-s-triazin-4-one
852
Synthesis of 8-(S)-methoxy-11-desmethyl laulimalide: a novel laulimalide analogue
853
Synthesis of 8,9-disubstituted fluoranthenes by domino two-fold Heck/electrocyclization/dehydrogenation of 1,2-dibromoacenaphthylene
854
Synthesis of 8-[18F]Fluoroguanine Derivatives: In Vivo Probes for Imaging Gene Expression with Positron Emission Tomography
855
Synthesis of 8-aminoadenosine 5′-(aminoalkyl phosphates), analogues of aminoacyl adenylates Original Research Article
856
Synthesis of 8-aryl substituted benzo[a]phenanthridine derivatives by consecutive three component tandem reaction and 6-endo carbocyclization
857
Synthesis of 8-arylated catechin and epicatechin derivatives via Suzuki cross-coupling
858
Synthesis of 8-arylsulfoxyl/sulfonyl adenines
859
Synthesis of 8-azidooctyl glycoside derivatives of the O-chain repeating unit of Escherichia coli O9a lipopolysaccharide and a methylated analog Original Research Article
860
Synthesis of 8-C-glucosylflavones Original Research Article
861
Synthesis of 8-chloro-benzo[c]quinolizin-3-ones as potent and selective inhibitors of human steroid 5α-reductase 1
862
Synthesis of 8-geranyloxypsoralen analogues and their evaluation as inhibitors of CYP3A4 Original Research Article
863
Synthesis of 8-hydroxyquinoline functionalised DO3A ligand and Eu(III) and Er(III) complexes: Luminescence properties
864
Synthesis of 8-O-alkylshikonin(alkannin)s: new ketal formation, tautomerism, and nucleophilic aromatic substitution
865
Synthesis of 8-oxa analogues of norcocaine endowed with interesting cocaine-like activity
866
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
867
Synthesis of 8-substituted 5H,9H-6-oxa-7-aza-benzocyclononene-10,11-dione-11-O-methyloximes, a new [1,2]-oxazonine ring system
868
Synthesis of 8-Substituted 7-Azarutaecarpines
869
Synthesis of 8-substituted bicyclo[3.2.1]octane-6-carboxylic acids and anti-convulsant properties of the corresponding amides
870
Synthesis of 8-substituted xanthines via 5,6-diaminouracils: an efficient route to A2A adenosine receptor antagonists
871
Synthesis of 8-thiabicyclo[3.2.1]oct-2-enes and their binding affinity for the dopamine and serotonin transporters
872
Synthesis of 8-vinyladenosine 5′-di- and 5′-triphosphate: evaluation of the diphosphate compound on ribonucleotide reductase
873
Synthesis of 9- and 10-membered macrolactones by selective ozonolysis of 1,4-diazaphenanthrene derivatives
874
Synthesis of 9-(2-β-C-methyl-β-d-ribofuranosyl)-6-substituted purine derivatives as inhibitors of HCV RNA replication
875
Synthesis of 9,9′-biphenanthryl-10,10′-bis(oxazoline)s and their preliminary evaluations in the Friedel–Crafts alkylations of indoles with nitroalkenes
876
Synthesis of 9-[2-O-(2-Methoxyethyl)-β-D-Ribofuranosyl]purines Using 1-Methanesulfonyloxy-2-Methoxyethane
877
Synthesis of 99mTc(CO)3-deoxyuridine derivatives as potential HSV1-tk gene expression imaging agents
878
Synthesis of 99mTc-ciprofloxacin by different methods and its biodistribution
879
Synthesis of 9-alkyl and 9-heteroalkyl substituted 2-amino-6-guanidinopurines and their influence on the NO-production in macrophages Original Research Article
880
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
881
Synthesis of 9-anthrylmethyl-functionalised cyclopentadienyl derivatives of rhodium(I) and iridium(I) and study of their luminescence properties
882
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
883
Synthesis of 9-ethynyl-9-fluorenol and its derivatives for crystallographic and optical properties study
884
Synthesis of 9H-fluoren-9-yl benzodithioates and their application as reversible addition–fragmentation chain transfer agents in living radical polymerization of styrene
885
Synthesis of 9-membered masked enediyne analogues possessing DNA intercalator and sugar moieties
886
Synthesis of 9-oxa-noradamantane derivative, an aesthetically pleasing ‘oxa-basket’
887
Synthesis of 9-oxime-11,12-carbamate ketolides Through a novel N-deamination reaction of 11,12-hydrazonocarbamate ketolide Original Research Article
888
Synthesis of 9-oxiranyl-9H-purine derivatives in β-cyclodextrin cavity
889
Synthesis of 9-substituted tetrahydrodiazepinopurines—asmarine A analogues
890
Synthesis of 9-substituted xanthenes by the condensation of arynes with ortho-hydroxychalcones
891
Synthesis of a (+)-anatoxin-a analogue for monoclonal antibodies production
892
Synthesis of a (B12H11S)2− containing glucuronoside as potential prodrug for BNCT
893
Synthesis of a (piperazin-1-ylmethyl)biaryl library via microwave-mediated Suzuki–Miyaura cross-couplings
894
Synthesis of a (thienylethenyl)benzimidazole platinum acetylide complex
895
Synthesis of a (β-acetamido-α-acetoxyethyl)boronic ester via azido boronic esters
896
Synthesis of a [18F]labeled chelidonine derivative as a possible antitumor agent
897
Synthesis of a [2]benzazepine analogue of clavizepine
898
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
899
Synthesis of a [3.3]biphenylophane, and its photophysical and photochemical properties studied by emission and transient absorption measurements
900
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
901
Synthesis of a ‘direct-linked’ C-disaccharide from a pyranulose glycoside
902
Synthesis of a ‘twisted’ transition-state analogue of biotin
903
Synthesis of a 1,3,4,5-tetrahydrobenzindole β-ketoester
904
Synthesis of a 1,3,5-benzotriazepine-2,4-dione based library
905
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
906
Synthesis of a 10-membered ring with eleutheside functionality by Nozaki–Hiyama–Kishi coupling
907
Synthesis of a 13C,15N labeled imidazole and characterization of the 2,5-endoperoxide and its decomposition
908
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
909
Synthesis of a 188Re-HEDP complex using carrier-free 188Re, and a study of its stability
910
Synthesis of a 1α-amino-1-deoxy analogue of forskolin
911
Synthesis of a 1α-C-methyl analogue of 25-hydroxyvitamin D3: interaction with a mutant vitamin D receptor Arg274Leu
912
Synthesis of a 200-member library of squaric acid N-hydroxylamide amides
913
Synthesis of a 2-benzocymantrenylpyridine and further mechanistic insights
914
Synthesis of a 2-indolylphosphonamide derivative with inhibitory activity against yersiniabactin biosynthesis
915
Synthesis of a 3′-naphthamido-LacNAc fluorescein conjugate with high selectivity and affinity for galectin-3 Original Research Article
916
Synthesis of a 3-aminopiperidin-2,5-dione as a conformationally constrained surrogate of the Ala-Gly dipeptide
917
Synthesis of a 3-deoxy-l-iduronic acid containing heparin pentasaccharide to probe the conformation of the antithrombin III binding sequence Original Research Article
918
Synthesis of a 4′,4′-spirothietane-2′, N3-cycloadenosine as a highly constrained analogue of 5′-deoxy-5′-methylthioadenosine (MTA)
919
Synthesis of a 5-alkoxypyrido[3,4-d]pyrimidin-4(3H)-one derivative via directed ortho-metallation of a pyridine analogue
920
Synthesis of a 5-alkoxypyrido[4,3-d]pyrimidin-4(3H)-one derivative via a regioselective Meisenheimer N-oxide rearrangement
921
Synthesis of a 6V-sulfated mannopentasaccharide analogue related to PI-88 Original Research Article
922
Synthesis of a Ag–AgBiTe hybrid nano-segmented structure by a galvanic displacement reaction
923
Synthesis of a benzothiadiazole/thiophene-based oligomer for bulk heterojunction photovoltaic cells
924
Synthesis of a benzotriazole azo dye phosphoramidite for labelling of oligonucleotides
925
Synthesis of a benzotriazole phosphoramidite for attachment of oligonucleotides to metal surfaces
926
Synthesis of a benzyl-protected analog of arenarioside, a trisaccharide phenylpropanoid glycoside Original Research Article
927
Synthesis of a BF2 complex of indol-2-yl-isoindol-1-ylidene-amine: a fully conjugated azadipyrromethene
928
Synthesis of a bicontinuous electrically conductive nanocomposite via in-situ formation of RuO2 nanoparticles
929
Synthesis of a bicyclic analog of l-iduronic acid adopting the biologically relevant 2S0 conformation Original Research Article
930
Synthesis of a bicyclic double-headed nucleoside
931
Synthesis of a bicyclo[5.3.1]undecene by a facile domino enyne cross-metathesis/IMDA
932
Synthesis of a bifunctional hapten designed to mimic both transition state and to induce “bait and switch” catalysis
933
Synthesis of a binuclear copper(II) compound and its use as a copper source for preparation of an environmental catalyst
934
Synthesis of a bio-based polyamidoamine-epichlorohydrin resin and its application for soy-based adhesives
935
Synthesis of a Biochemically Important Aldehyde, 3,4-Dihydroxyphenylacetaldehyde
936
Synthesis of a Biochemically Important Aldehyde, 3,4-Dihydroxyphenylglycolaldehyde
937
Synthesis of a biocompatible gelatin functionalized graphene nanosheets and its application for drug delivery
938
Synthesis of a biocompatible polymer using siloxane-based surfactants in supercritical carbon dioxide
939
Synthesis of a biologically active isomer of kotalanol, a naturally occurring glucosidase inhibitor Original Research Article
940
Synthesis of a bioprobe for elucidation of target molecule of spongean anti-malarial peroxides
941
Synthesis of a biotinated amphiphile
942
Synthesis of a biotin-conjugate of phosmidosine O-ethyl ester as a G1 arrest antitumor drug Original Research Article
943
Synthesis of a biotin-tagged photoaffinity probe of 2-azetidinone cholesterol absorption inhibitors Original Research Article
944
Synthesis of a biotinylated camptothecin derivative and determination of the binding sequence by T7 phage display technology
945
Synthesis of a biphenyl library for studies of hydrogen bonding in the solid state
946
Synthesis of a biphenyl-based axially chiral amino acid as a highly efficient catalyst for the direct asymmetric aldol reaction
947
Synthesis of a biphenyl-based cyclophane via benzidine rearrangement of a constrained m-nitrophenol derivative
948
Synthesis of a bipyridine-derived achiral thiourea trifluoromethanesulfonic acid salt and its application as an additive in organocatalytic asymmetric reactions
949
Synthesis of a bis(diketiminate)bromosamarium(III) complex and its activity in the polymerization of methyl methacrylate Original Research Article
950
Synthesis of a bis-(N-sec-butyl-dithiocarbamato)-nitrido-99mTc complex: a potential new radiopharmaceutical for brain perfusion studies
951
Synthesis of a bis(phenoxyketimine) palladium(II) complex and its activity in the Suzuki–Miyaura reaction
952
Synthesis of a bis-azido analogue of acromelic acid for radioisotope-free photoaffinity labeling and biochemical studies
953
Synthesis of a bi-structured hybrid in a CaO–SiO2-PTMO system and in vitro evaluation on its potential of bone-bonding property
954
Synthesis of a bis-vinylogous chlorin possessing a fused naphthalene ring
955
Synthesis of a boron analogue of glucose-conjugated nucleoside diphosphate: nucleoside α-P-boranodiphosphoglucose
956
Synthesis of a boron analogue of glucose-conjugated nucleoside diphosphate: nucleoside α-P-boranodiphosphoglucose
957
Synthesis of a boron analogue of glucose-conjugated nucleoside diphosphate: nucleoside α-P-boranodiphosphoglucose
958
Synthesis of a boronated amino acid as a potential neutron therapy agent: 1-amino-3-[(dihydroxyboryl)ethyl]cyclobutanecarboxylic acid
959
Synthesis of a boron-containing conducting polymer from the anodic oxidation of Tris(pyrrolyl)borane
960
Synthesis of a branched chain aza-C-disaccharide via the cycloaddition of a chiral nitrone to an alkene, both sugar derivatives
961
Synthesis of a bromotyrosine-derived natural product inhibitor of mycothiol-S-conjugate amidase
962
Synthesis of a building block for phosphonate analogues of moenomycin A12 from d-tartaric acid
963
Synthesis of a building block for phosphonate analogues of moenomycin A12 from d-tartaric acid
964
Synthesis of a C(4)–C(9) eleutheside template from d-glucal
965
Synthesis of a C1 symmetric BINOL–terpyridine ligand and highly enantioselective methyl propiolate addition to aromatic aldehydes
966
Synthesis of a C1–C9 fragment of rhizoxin
967
Synthesis of a C1-symmetric Box macrocycle and studies towards active-template synthesis of mechanically planar chiral rotaxanes
968
Synthesis of a C3-symmetric (1→6)-N-acetyl-β-d-glucosamine octadecasaccharide using click chemistry Original Research Article
969
Synthesis of a C3-symmetric ferrocenylphosphine and its application to the Suzuki reaction of aryl chlorides
970
Synthesis of a C3-symmetric macrocycle with alternating sugar amino acid and tyrosine residues
971
Synthesis of a C8 oxygenated pyranonaphthoquinone: a useful precursor to dimeric pyranonaphthoquinones
972
Synthesis of a caged glutamate for efficient one- and two-photon photorelease on living cells
973
Synthesis of a cam system for the measurement and follow rest of multi-step shaft necks at machining
974
Synthesis of a carbamide-based dithiocarbamate chelator for the removal of heavy metal ions from aqueous solutions
975
Synthesis of a carbon monolith with trimodal pores
976
Synthesis of a carbon nanofiber/carbon foam composite from coal liquefaction residue for the separation of oil and water Original Research Article
977
Synthesis of a carbon nanotube monolith with controlled macroscopic shape
978
Synthesis of a carbon replica of zeolite Y with large crystallite size
979
Synthesis of a carbon-14 analogue of 8-chloro-11-(4-methyl-1-piperazinyl)-11-[14C]-dibenz[b,f][1,4]oxazepine
980
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
981
Synthesis of a carbon-coated NiO/MgO core/shell nanocomposite as a Pd electro-catalyst support for ethanol oxidation
982
Synthesis of a carboxyl linker containing Pk trisaccharide Original Research Article
983
Synthesis of a carotenobenzoporphyrin from a meso-diphenylporphyrin
984
Synthesis of a caryophyllene isoprenologue, a potential diterpene natural product
985
Synthesis of a cationic pyridoxamine conjugation reagent and application to the mechanistic analysis of an artificial transaminase
986
Synthesis of a cell-permeable analogue of a glycosylphosphatidylinositol (GPI) intermediate that is toxic to the living bloodstream form of Trypanosoma brucei
987
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
988
Synthesis of a C-galactopyranosyl-linked N-substituted 1,2-ethylenediamine
989
Synthesis of a C-glucosylated cyclopropylamide and evaluation as a glycogen phosphorylase inhibitor
990
Synthesis of a C-glycosylpyranonaphthoquinone related to medermycin
991
Synthesis of a chemiluminescent probe useful for the purification of steroid 5α-reductase
992
Synthesis of a chiral alcohol using a rationally designed Saccharomyces cerevisiae reductase and a NADH cofactor regeneration system
993
Synthesis of a chiral micelle-like dendrimer with phenylene dendrons and a 1,1′-binaphthyl core
994
Synthesis of a chiral steroid ring D precursor starting from carvone
995
Synthesis of a chitin-based biocomposite for water treatment: Optimization for fluoride removal
996
Synthesis of a chitosan derivative soluble at neutral pH and gellable by freeze–thawing, and its application in wound care
997
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
998
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
999
Synthesis of a chitosan-linked calix[4]arene chelating polymer and its sorption ability toward heavy metals and dichromate anions
1000
Synthesis of a chlorogenin glycoside library using an orthogonal protecting group strategy Original Research Article
