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1
Synthesis of 2,5-dihalothiazole-4-carboxylates
2
Synthesis of 2,5-dihydrobenzo[b]oxepines and 5,6-dihydro-2H-benzo[b]oxocines based on a ‘[3+3] cyclization-olefin-metathesis’ strategy
3
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)
4
Synthesis of 2,5-disubstituted-3-cyanoindoles
5
Synthesis of 2,5-thiazole butanoic acids as potent and selective αvβ3 integrin receptor antagonists with improved oral pharmacokinetic properties
6
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
7
Synthesis of 2,6-bis(4R-trialkylsiloxymethyloxazolinyl)pyridines and their use in catalytic asymmetric 1,3-dipolar cycloaddition reactions of nitrones and activated alkenes
8
Synthesis of 2,6-cis-disubstituted 4-methylenetetrahydropyrans by oxy-Michael addition
9
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
10
Synthesis of 2,6-diaryl-1,2-dihydropyridines through a 6π-electrocyclization of N-sulfonylazatrienes
11
Synthesis of 2,6-diaryl-3-(trifluoromethyl)pyridines by regioselective Suzuki–Miyaura reactions of 2,6-dichloro-3-(trifluoromethyl)pyridine
12
Synthesis of 2,6-diaryl-4,4-diphenyldithienosiloles and their luminescent properties
13
Synthesis of 2,6-dichlorobenzonitrile from 2,6-dichlorotoluene by gas phase ammoxidation over VPO catalysts
14
Synthesis of 2,6-dimethyl-9-aryl-9-phosphabicyclo[3.3.1]nonanes: their application to asymmetric synthesis of chiral tetrahydroquinolines and relatives
15
Synthesis of 2,6-dimethylnaphthalene by methylation of methylnaphthalene on various medium and large-pore zeolite catalysts Original Research Article
16
Synthesis of 2,6-dioxabicyclo[3.3.0]octenes by tandem ring-rearrangement/cross metathesis
17
Synthesis of 2,6-dioxatricyclo[3.3.1.03,7]nonanes by intramolecular haloetherification and/or transannular hydroxycyclization of alkenes in [4+3]-cycloadducts
18
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
19
Synthesis of 2,6-disubstituted dihydropyrans via an efficient BiBr3-initiated three component, one-pot cascade
20
Synthesis of 2,6-disubstituted morpholines through regioselective oxiranes ring opening by tosylamide under PTC conditions
21
Synthesis of 2,6-disubstituted piperidine alkaloids from ladybird beetles Calvia 10-guttata and Calvia 14-guttata
22
Synthesis of 2,6-disubstituted pyrido[2,3-b][1,4]oxazines
23
Synthesis of 2,6-disubstituted-7,8-dihydro-6H-pyrano[2,3-6]pyrazines
24
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
25
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
26
Synthesis of 2-[(Z)-1-hydropolyfluoro-1-alkenyl]-4H-3,1-benzoxazin-4-ones
27
Synthesis of 2-[18F]fluoro-image-tyrosine via regiospecific fluoro-de-stannylation
28
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
29
Synthesis of 2-[3,5-substituted pyrazol-1-yl]-4,6-trisubstituted triazine derivatives as antimalarial agents
30
Synthesis of 2-[4-(substituted benzylidene)-5-Oxo- 4,5-dihydro-oxazol-2-ylmethyl]-isoindole-1,3-dione Derivatives as Novel Potential Antimicrobial Agents
31
Synthesis of 2-[5-amino-2,3-dihydro-4H-imidazol-4-ylidene]malononitriles
32
Synthesis of 2-[6-(2,4-Dinitrophenoxy)hexyl]oxiranecarboxylic acid: A selective carnitine palmitoyltransferase-1 inhibitor Original Research Article
33
Synthesis of 2’-(5-Chloro-2-Hydroxybenzylidene) Benzenesulfanohydrazide Schiff Base and its Anti-Ulcer Activity in Ethanol-Induced Gastric Mucosal Lesions in Rats
34
Synthesis of 2′,3′-dideoxy-2′-monofluoromethyl azanucleosides Original Research Article
35
Synthesis of 2′,3′-dideoxy-3′,4′-dihydroxymethyl substituted pyrimidine nucleoside analogues
36
Synthesis of 2′,3′-dideoxy-3′-C-(hydroxymethyl)-4′-thiopentofuranosyl nucleosides as potential antiviral agent
37
Synthesis of 2′,3′-dideoxy-3′-fluoro-l-ribonucleosides as potential antiviral agents from d-sorbitol Original Research Article
38
Synthesis of 2′,3′-dideoxy-6′,6′-difluoro-3′-azanucleosides
39
Synthesis of 2′,3′-dideoxy-6′-fluorocarbocyclic nucleosides via Reformatskii–Claisen rearrangement
40
Synthesis of 2′,3′-dideoxynucleosides via C–S bond cleavage: N-glycosylation of 2,3-dideoxy-1-[(2-pyridylmethyl)thio]glycoside
41
Synthesis of 2′,3′-dihydrosolanesyl analogues of β-d-arabinofuranosyl-1-monophosphoryldecaprenol with promising antimycobacterial activity
42
Synthesis of 2′,5′-oligoadenylate analogs containing an adenine acyclonucleoside and their ability to activate human RNase L
43
Synthesis of 2′-aminoalkyl-1-benzylisoquinoline derivatives and medium sized ring analogues with mu opiod receptor binding activities
44
Synthesis of 2′-C-methyl-branched isonucleosides
45
Synthesis of 2′-C-α-difluoromethylarauridine and its 3′-O-phosphoramidite incorporation into a hammerhead ribozyme
46
Synthesis of 2′-dealkylmumbaistatin
47
Synthesis of 2′-deoxy-2′-fluororibo- and 2′-deoxy-2′,2′-difluororibonucleosides derived from 6-(het)aryl-7-deazapurines
48
Synthesis of 2′-deoxyibosylnucleosides using new 2′-deoxyribosyltransferase microorganism producers
49
Synthesis of 2′-deoxyuridine 5′-(α,β-imido)triphosphate: a substrate analogue and potent inhibitor of dUTPase Original Research Article
50
Synthesis of 2′-hydrazine oligonucleotides and their efficient conjugation with aldehydes and 1,3-diketones
51
Synthesis of 2′-O,3′-O bicyclic adenosine analogues using ring closing metathesis
52
Synthesis of 2′-O-[2-[(N,N-dialkylamino)oxy]ethyl]-modified oligonucleotides: hybridization affinity, resistance to nuclease, and protein binding characteristics
53
Synthesis of 2′-O-modified adenosine building blocks and application for RNA interference Original Research Article
54
Synthesis of 2′-O-α-d-ribofuranosyladenosine, monomeric unit of poly(ADP–ribose)
55
Synthesis of 2′-paclitaxel methyl 2-glucopyranosyl succinate for specific targeted delivery to cancer cells
56
Synthesis of 2′-β-C-methyl toyocamycin and sangivamycin analogues as potential HCV inhibitors
57
Synthesis of 2′-β-C-methyl-neplanocin derivatives as anti-HCV agents
58
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
59
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
60
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
61
Synthesis of 21,31-O-(propane-1,2-diyl)- and 21,31-O-(3-hydroxypropane-1,2-diyl)-cyclomaltoheptaose
62
Synthesis of 21-nor-22-oxa-1α,25-dihydroxyvitamin D3 derivatives in quest of a drug with low calcemic activity
63
Synthesis of 21-oxoporphyrin building blocks and energy donor appended systems
64
Synthesis of 21-thia and 21-oxaporphyrin building blocks and boron–dipyrrin appended systems
65
Synthesis of 22-oxaspiro[4.5]decane CD-ring modified analogs of 1α,25-dihydroxyvitamin D3
66
Synthesis of 25-aminosterols, new antifungal agents
67
Synthesis of 26,27-bisnorcastasterone analogs and analysis of conformation–activity relationship for brassinolide-like activity Original Research Article
68
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
69
Synthesis of 28-19F-amphotericin B methyl ester
70
Synthesis of 2-acetamido-1,2-dideoxy-d-galacto-nojirimycin [DGJNAc] from d-glucuronolactone: the first sub-micromolar inhibitor of α-N-acetylgalactosaminidases
71
Synthesis of 2-acetamido-2-deoxy-5-thio-β-d-altropyranose
72
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)
73
Synthesis of 2-acetamido-3-O-acetyl-2-deoxy-d-mannose phosphoramidites
74
Synthesis of 2-acetoxy[5]helicene by sequential double aromatic oxy-Cope rearrangement
75
Synthesis of 2-acylamino-2-deoxy-d-glucofuranoses and their transformation into hex-2-enofuranoses
76
Synthesis of 2-acylindole-3-acetic acids: a novel base-mediated indole synthesis
77
Synthesis of 2-alkoxy-8-hydroxyadenylpeptides: Towards synthetic epitope-based vaccines
78
Synthesis of 2-alkoxymethyl-3-trifluoromethyl-1,4-naphthoquinones
79
Synthesis of 2-alkyl (and aryl)-1-aryl-2-propen-1-ones via m-CPBA mediated oxidation of γ-(benzotriazol-1-yl)allylic selenides
80
Synthesis of 2-alkyl-2-arylcyanoacetates via CuI/sodium picolinate-catalyzed direct arylation of α-substituted cyanoacetates
81
Synthesis of 2-alkyl-3-aryl-substituted quinuclidines as novel dopamine transporter inhibitors
82
Synthesis of 2-alkylidene-cycloalkane-1,3-diols via enantioselective intramolecular carbolithiation
83
Synthesis of 2-alkylidenetetrahydrofurans by Ru-catalyzed regio- and stereoselective codimerization of dihydrofurans with ,(alpha),(beta)-unsaturated esters
84
Synthesis of 2-alkynylquinolines from 2-chloro and 2,4-dichloroquinoline via Pd/C-catalyzed coupling reaction in water
85
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
86
Synthesis of 2-amido-3-hydroxypyridin-4(1H)-ones: novel iron chelators with enhanced pFe3+ values Original Research Article
87
Synthesis of 2-amino-1,3,4-oxadiazoles from isoselenocyanates via cyclodeselenization
88
Synthesis of 2-amino-1,3-dienes by chromium-catalyzed addition of silylated propargyl bromides to imines
89
Synthesis of 2-amino-1,3-diols incorporating the cyclobutane ring
90
Synthesis of 2-amino-2,4-anhydro-3-O-(2-tetrahydropyranyl)-psicofuranose: a versatile intermediate for S-type locked nucleosides
91
Synthesis of 2-Amino-3,5-dicarbonitrile-6-thiopyridines Using Silica-bonded N-Propyldiethylenetriamine as a Heterogeneous Solid Base Catalyst
92
Synthesis of 2-amino-3-cyano-4H-chromen-4-ylphosphonates and 2-amino-4H-chromenes catalyzed by tetramethylguanidine
93
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
94
Synthesis of 2-amino-4-(4-methoxyphenyl)-1,3-thiazole coatedmagnetic nanoparticles: A potential antibacterial compound
95
Synthesis of 2-amino-4-(7-azaindol-3-yl)pyrimidines as cyclin dependent kinase 1 (CDK1) inhibitors
96
Synthesis of 2-amino-4,6-diarylnicotininitriles using 3-propyldiethylenetriamine-silica as a recyclable solid base catalyst
97
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
98
Synthesis of 2-Amino-4H-chromene Derivatives under Solvent-Free Condition Using MOF-5
99
Synthesis of 2-amino-4H-pyran derivatives in aqueous media with nano-SnO2 as recyclable catalyst
100
Synthesis of 2Amino4hydroxy1HPyrrole3Carbonitrile from Glycine Under Microwave Irradiation
101
Synthesis of 2-amino-5-alkylidenethiazol-4-ones from ketones, rhodanine, and amines with the aid of re-usable heterogeneous silica-pyridine based catalyst
102
Synthesis of 2-amino-5-chloro-3-(trifluoromethyl)benzenethiol and conversion into 4H-1,4-benzothiazines and their sulfones
103
Synthesis of 2-amino-5-substituted-1,3,4-oxadiazoles using 1,3-dibromo-5,5-dimethylhydantoin as oxidant
104
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
105
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
106
Synthesis of 2-amino-8-chloro-4-phenyl-5,11-dihydro-6H-pyrido[2,3-a]carbazole-3-carbonitrile: Structural and biological evaluation
107
Synthesis of 2-aminoazulene derivatives. Nucleophilic and palladium-catalyzed amination of 2-substituted azulene
108
Synthesis of 2-aminobenzoxazoles via copper-catalyzed electrophilic amination of benzoxazoles with O-benzoyl hydroxylamines
109
Synthesis of 2-aminocyclopropyl pyrrolidines from glycoaminonitriles
110
Synthesis of 2-aminoethyl-5-carbethoxythiazoles utilizing a Michael-like addition strategy
111
Synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolin-1-ols and their conversion to 7-aryl-9H-6-oxa-5,8-diaza-benzocycloheptenes
112
Synthesis of 2-aryl-1h-benzimidazole derivatives using nano montmorillonite clay as an efficient catalyst
113
Synthesis of 2-aryl1-H-benzo[d]imidazole derivatives using nano montmorillonite clay as an efficient catalyst
114
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
115
Synthesis of 2-aryl-2H-indazoles by base catalysed reaction of 2-nitrobenzyl triphenylphosphonium bromide and aryl isocyanates
116
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
117
Synthesis of 2-aryl-3-hydroxymethyl-5,5-difluoropiperidines
118
Synthesis of 2-aryl-4-chloropyrroles via ring expansion of 2-aryl-1-chlorocyclopropanecarbaldehydes
119
Synthesis of 2-aryl-4H-pyrano[2,3-b]pyridin-4-ones by a one-pot deprotection–cyclization reaction
120
Synthesis of 2-aryl-6-methyl-5-nitroquinoline derivatives as potential prodrug systems for reductive activation
121
Synthesis of 2-arylacrylic esters from aryl methyl ketones via Wittig reaction/singlet oxygen ene reaction
122
Synthesis of 2-arylbenzimidazoles via microwave Suzuki–Miyaura reaction of unprotected 2-chlorobenzimidazoles
123
Synthesis of 2-arylbenzoxazoles via DDQ promoted oxidative cyclization of phenolic Schiff bases—a solution-phase strategy for library synthesis
124
Synthesis of 2-aryl-imidazo[4,5-d][1,2,3]triazoles from a 4-nitro-imidazol-5-yl phosphoramidate and aryl isocyanates
125
Synthesis of 2-arylpropionic acids by electrocarboxylation of benzylchlorides catalysed by PdCl2(PPh3)2
126
Synthesis of 2-azaspiro[4.4]nonan-1-ones via phosphine-catalysed [3+2]-cycloadditions
127
Synthesis of 2-azidoethyl α-d-mannopyranoside orthogonally protected and selective deprotections
128
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
129
Synthesis of 2-benzyl-2H-pyrazole-3,4-diamine dihydrochloride
130
Synthesis of 2-benzylimidazo[2,1-b][1,3]benzothiazoles through palladium-catalyzed heteroannulation of acetylenic compounds
131
Synthesis of 2-boryl-1,3-butadienes from tributylphosphine stabilized zirconacyclopropenes and alkynes
132
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
133
Synthesis of 2-bromo-1H-indenes via copper-catalyzed intramolecular cross-coupling of gem-dibromoolefins
134
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
135
Synthesis of 2-chloro-1,1-difluoroallyl mesylates through novel rearrangement and CC bond formation by their Pd-catalyzed reaction with diethylzinc
136
Synthesis of 2-chloro-4-nitrophenyl α-l-fucopyranoside: a substrate for α-l-fucosidase (AFU)
137
Synthesis of 2-chloro-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one
138
Synthesis of 2-C-hydroxymethylribofuranosylpurines as potent anti-hepatitis C virus (HCV) agents
139
Synthesis of 2-C-methylerythritols and 2-C-methylthreitols via enantiodivergent Sharpless dihydroxylation of trisubstituted olefins
140
Synthesis of 2-C-trifluoromethyl substituted d-ribose
141
Synthesis of 2-cyano-1,4-cycloheptadiene derivatives via divinylcyclopropane rearrangement and alkylation of novel cycloheptadienyl anion species
142
Synthesis of 2D metal–organic coordination polymers with large internal cavities and their magnetic properties
143
Synthesis of 2D polymeric dicyanamide bridged hexa-coordinated Cu(II) complex: Structural characterization, spectral studies and TDDFT calculation
144
Synthesis of 2-Dehydro-3-epi-20-hydroxyecdysone
145
Synthesis of 2-deoxy cyclic and linear oligosaccharides by oligomerization of monomers Original Research Article
146
Synthesis of 2-deoxy-2-(4-nitroimidazol-1-yl)-d-alditols
147
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
148
Synthesis of 2-Deoxy-2-C-Alkylglucosides of myo-Inositol as possible inhibitors of a N-Deacetylase enzyme in the biosynthesis of mycothiol
149
Synthesis of 2-deoxy-2-fluoro analogs of polyprenyl β-d-arabinofuranosyl phosphates
150
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
151
Synthesis of 2-deoxy-2-fluoro-glucotropaeolin, a thioglucosidase inhibitor
152
Synthesis of 2-deoxy-2-fluoro-phosphatidylinositol-4,5-bisphosphate and analogues: Probes and modulators of the mammalian PI-PLCS
153
Synthesis of 2-deoxy-d-arabino/lyxo-hexopyranosyl disaccharides Original Research Article
154
Synthesis of 2-deoxy-hexopyranosyl derivatives of uridine as donor substrate analogues for glycosyltransferases
155
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)
156
Synthesis of 2-Diphenylphosphinoyl-2 -Halo Biphenyls Via Suzuki-Miyaura Coupling as Possible Route to Non-Symmetric Biphenyl Phosphines
157
Synthesis of 2-diphenylphosphinoyl-3,5-(diaryl)-3,4-dihydro-2H-thiopyrans by the reaction of a bis[(diphenylphosphinoyl)methyl]sulfide with chalcones
158
Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride
159
Synthesis of 2E,4E,6E,11Z-octadecatetraenoic acid of the Rhizobium leguminosarum biovar viciae Nod factor
160
Synthesis of 2-ethyl-2-hexenal oxime and its flotation performance for copper ore
161
Synthesis of 2-ferrocenylquinoline derivatives and evaluation of their antimalarial activity
162
Synthesis of 2-fluoro and 4-fluoro galactopyranosyl phosphonate analogues of UDP-Gal Original Research Article
163
Synthesis of 2-fluoronoraristeromycin and its inhibitory activity against Plasmodium falciparum S-Adenosyl- -homocysteine hydrolase
164
Synthesis of 2-fluorotetralones by oxidative radical cyclization of α-fluoroacetophenones and olefins
165
Synthesis of 2H-1,2-oxaphosphorin 2-oxides
166
Synthesis of 2H-1,4-benzothiazin-3(4H)-ones and 2H-1,4-benzoselenazin-3(4H)-ones with the aid of samarium(II) iodide
167
Synthesis of 2H-1,5-benzodioxepin and 2,5-dihydro-1,6-benzodioxocin derivatives via ring-closing metathesis reaction
168
Synthesis of 2-halo-2H-azirines
169
Synthesis of 2H-chromenes and 1,2-dihydroquinolines from aryl aldehydes, amines, and alkenylboron compounds
170
Synthesis of 2H-pyrroles by treatment of pyrrolidines with DDQ
171
Synthesis of 2H-pyrroles via the 1,3-dipolar cycloaddition reaction of nitrile ylides with acrylamides
172
Synthesis of 2-hydroxy acid from 2-amino acid by Clostridium butyricum
173
Synthesis of 2-hydroxy-3-indolinones and 3-hydroxy-2-indolinones by anionic cyclization, in situ oxidation and rearrangement
174
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
175
Synthesis of 2-hydroxy-3-substituted naphthoquinones using the Heck reaction
176
Synthesis of 2-imidazolidinylidene propanedinitrile derivatives as stimulators of gastrointestinal motility—III Original Research Article
177
Synthesis of 2-iminothiazoline derivatives by sequential conjugate addition/annulation/ring-opening reactions
178
Synthesis of 2-iodo- and 2-phenyl-[11C]melatonin: potential PET tracers for melatonin binding sites
179
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
180
Synthesis of 2-iodoynamides and regioselective [2+2] cycloadditions with ketene
181
Synthesis of 2-isoxazoline and α-hydroxy ketomethylene dipeptide isosteres Original Research Article
182
Synthesis of 2-mercapto-3-substituted-5,6-dimethylthieno[2,3-d] pyrimidin-4(3H)-ones as new analgesic, anti-inflammatory agents
183
Synthesis of 2-Mercaptobenzimidazole and Some of its Derivatives
184
Synthesis of 2-mesityl-3-methylpyrrole via the Trofimov reaction for a new BODIPY with hindered internal rotation
185
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
186
Synthesis of 2-methyl- and 2-methylenecyclobutane amino acids
187
Synthesis of 2-methyl-4-methoxydiphenylamine by palladium catalyzed C–N coupling—high synthetic versatility by use of a flexible catalytic system
188
Synthesis of 2-methylidene-1-silacyclohexanes by intramolecular hydrosilylation
189
Synthesis of 2-methylidene-1-silacyclohexanes from 2,6-dibromohex-1-ene and polyhalosilanes
190
Synthesis of 2-modified aristeromycins and their analogs as potent inhibitors against Plasmodium falciparum S-adenosyl-l-homocysteine hydrolase Original Research Article
191
SYNTHESIS OF 2-MONO- AND 2,7-DISUBSTITUTED-1,8-DIHYDROXY9-ANTHRONES, A NOVEL MEMBER OF THE ANTHRONE CLASS OF ANTIPSORIATIC AGENTS
192
Synthesis of 2-monoacylglycerols and structured triacylglycerols rich in polyunsaturated fatty acids by enzyme catalyzed reactions
193
Synthesis of 2-N-alkyl(aryl)amino-7-nitrobenzothiazoles
194
Synthesis of 2-naphthylacrylamides and 2-naphthylacrylates via homogeneous catalytic carbonylation of 1-iodo-1-naphthylethene derivatives
195
Synthesis of 2-NBDLG, a fluorescent derivative of l-glucosamine; the antipode of d-glucose tracer 2-NBDG
196
Synthesis of 2-N-substituted benzothiazoles via domino condensation-hetero cyclization process, mediated by copper oxide nanoparticles under ligand-free conditions
197
Synthesis of 2-O-(2-iodoethyl)-d-glucose, a stable iodinated analogue of 2-deoxy-2-fluoro-d-glucose
198
Synthesis of 2-O-heteroaroyl taxanes: evaluation of microtubule assembly promotion and cytotoxicity
199
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
200
Synthesis of 2-oxazolidinones by salen-Co-complexes catalyzed oxidative carbonylation of β-amino alcohols
201
Synthesis of 2-oxazolidones by sulfur-assisted thiocarboxylation with carbon monoxide and oxidative cyclization with molecular oxygen under mild conditions
202
Synthesis of 2-oxazolines and related N-containing heterocycles using [Et2NSF2]BF4 as a cyclodehydration agent
203
Synthesis of 2-oxazolines mediated by N,N′-diisopropylcarbodiimide
204
Synthesis of 2-oxazolines via boron esters of N-(2-hydroxyethyl) amides
205
Synthesis of 2-pentafluorosulfanylnaphthalene
206
Synthesis of 2-phenylethyl acetate in the presence of Yarrowia lipolytica KKP 379 biomass
207
Synthesis of 2-phenylquinoline-based ambipolar molecules containing multiple 1,3,4-oxadiazole spacer groups
208
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
209
Synthesis of 2-pyranosyl benzothiazoles, benzimidazoles and benzoxazoles via nucleophilic addition reactions of pyranosyl nitrile oxides
210
Synthesis of 2-pyranylidene or (2-furyl)carbene–chromium complexes from conjugated enyne carbonyl compounds with Cr(CO)5(THF)
211
Synthesis of 2-pyridones as tissue factor VIIa inhibitors
212
Synthesis of 2-pyrolyl-2-hydroxy-2-cyanoacetamide through FeCl3–TBHP mediated hydroxylation of captodative stabilized radical intermediate
213
Synthesis of 2-pyrone-4-carboxaldehydes from acetylene dicarboxaldehyde monoacetal
214
Synthesis of 2S-(2-hydroxyethyl)-3R-hydroxy-4S-(thymin-1-yl or adenin-9-yl)-tetrahydrofuran
215
Synthesis of 2-selenoxoperhydro-1,3-selenazin-4-ones via diselenocarbamate intermediates
216
Synthesis of 2-Substitued Benzimidazoles Using P2O5-SiO2
217
Synthesis of 2-Substitued Benzimidazoles Using P2O5-SiO2
218
Synthesis of 2-substituted -tryptophan-containing peptide derivatives with endothelin receptor antagonist activity
219
Synthesis of 2-substituted 1-benzyl-2,3,4,5-tetrahydro-1-benzazepines by palladium catalysis. Observation of a competitive β-hydride elimination pathway
220
Synthesis of 2-substituted 2H-chromenes using potassium vinyltrifluoroborates
221
Synthesis of 2-substituted 3-ethyl-3H-imidazo[4,5-b]pyridines catalyzed by Al3+-exchanged K10 clay as solid acids
222
Synthesis of 2-substituted bamipine derivatives
223
Synthesis of 2-Substituted Benzimidazoles and Bis-benzimidazoles by Microwave in the Presence of Alumina-Methanesulfonic Acid
224
Synthesis of 2-substituted chromenes via ring-closing metathesis and stable 1-benzopyrylium ions
225
Synthesis of 2-substituted endo-hymenialdisine derivatives
226
Synthesis of 2-substituted indoles by palladium-catalyzed heteroannulation with Pd–NaY zeolite catalysts
227
Synthesis of 2-substituted indoles via a palladium-catalyzed domino Heck reaction and dealkylation
228
Synthesis of 2-substituted piperazines via direct α-lithiation
229
Synthesis of 2-substituted pyrrolidines from nitriles
230
Synthesis of 2-substituted quinones, vitamin K3, and vitamin K1 from p-cresol. BF3·OEt2-catalyzed methyl migration of 4-tert-butyldioxycyclohexadienones
231
Synthesis of 2-substituted-7-azaindoles from 2-amino-3-picolin
232
Synthesis of 2-substituted-benzothiazoles by palladium-catalyzed intramolecular cyclization of o-bromophenylthioureas and o-bromophenylthioamides
233
Synthesis of 2-substituted-pyrrolidinethiourea derivatives and their antagonist effect on vanilloid receptor
234
Synthesis of 2-thioxoimidazolines via reaction of 1-unsubstituted 3-aminoquinoline-2,4-diones with isothiocyanates
235
Synthesis of 2-TIPS-oxazol-5-ylboronic acid pinacol ester: efficient route to 5-(het)aryloxazoles via Suzuki cross-coupling reaction
236
Synthesis of 2-trifluoromethoxyethyl trifluoromethoxyacetate and derived 2-trifluoromethoxyacrylates
237
Synthesis of 2-trifluoromethyl-1(substituted aryl)-4(1H)-quinolones using trifluoroacetamidoyl chlorides
238
Synthesis of 2-trifluoromethylthioacrylate and its derivatives via the Knoevenagel condensation
239
Synthesis of 2-ynamides by direct palladium-catalyzed oxidative aminocarbonylation of alk-1-ynes
240
Synthesis of 2α- and 2β-substituted-14-epi-previtamin D3 and their genomic activity
241
Synthesis of 3- and 5-amino-5-(3)-(pyrrol-2-yl)isoxazoles
242
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
243
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
244
Synthesis of 3-(1H-benzimidazol-2-yl)-5-isoquinolin-4-ylpyrazolo[1,2-b]pyridine, a potent cyclin dependent kinase 1 (CDK1) inhibitor
245
Synthesis of 3-(1H-benzo[d]imidazol-1-yl)isoindolin-1-one derivatives promoted by EtOH–AcOH solvent system
246
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
247
Synthesis of 3-(2-nitroalkyl) indoles by reaction of 3-(1-arylsulfonylalkyl) indoles with nitroalkanes
248
Synthesis of 3-(2-pyridyl)-2-substituted-quinazolin-4(3H)-ones as new analgesic and anti-inflammatory agents
249
Synthesis of 3-(3,4-dihydroxyphenyl)-propionic acid derivatives by N-coupling of amines using laccase
250
Synthesis of 3-(4-heteroaryl-phenyl)-8-oxabicyclo[3.2.1]octane-2-carboxylic acid methyl esters
251
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
252
Synthesis of 3-(benzylideneamino)-2-phenyl-5H-imidazo[1,2-b]pyrazole-7-carbonitriles via a four-component condensation reaction
253
Synthesis of 3-(Trifluoromethyl)benzo[c][1,6]naphthyridines from Substituted 4H-Pyran-4-ones via 4-Amino-5-Aryl-2-(trifluoromethyl)pyridines
254
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
255
Synthesis of 3-(Trimethoxysilyl)PropylMethacrylateFunctionalized GrapheneOxideBased Mixed MatrixMembrane andItsApplication for O2/N2Separation
256
Synthesis of 3-(α- and β-d-arabinofuranosyl)-6-chloro-1,2,4-triazolo[4,3-b]pyridazine Original Research Article
257
Synthesis of 3, 4-Dihydropyrimidin-2-(1H)-ones Using a Hydrogel as a Green and Reusable Catalyst
258
Synthesis of 3,20-disubstituted chlorophyll-a derivatives and reactivity of the substituents
259
Synthesis of 3,3,3-trifluoroprop-1-enyl compounds from some enolizable aldehydes
260
Synthesis of 3,3,4,4-tetrafluoro-1,2-bis(imino)cyclobutanes: A cyclic version of fluorinated α-diimines
261
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
262
Synthesis of 3,3′-neotrehalosadiamine and related 1,1′-aminodisaccharides using disarmed, armed, and superarmed building blocks
263
Synthesis of 3,3-bis(difluoramino)octahydro-1,5,7,7-tetranitro-1,5-diazocine (TNFX), a diversified energetic heterocycle
264
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
265
Synthesis of 3,3-disubstituted oxetane building blocks
266
Synthesis of 3,3-disubstituted oxindoles
267
Synthesis of 3,3-disubstituted oxindoles through Pd-catalyzed intramolecular cyanoamidation
268
Synthesis of 3,3-Disubstituted-2,2-bipyridines from 1,10-Phenanthroline-5,6-quinone
269
Synthesis of 3,4,5-trisubstituted indoles via iterative directed lithiation of 1-(triisopropylsilyl)gramines
270
Synthesis of 3,4-diaryl-1-phenyl-4,5-dihydro-1H-pyrazole-5-carbonitriles via 1,3-dipolar cycloaddition reactions
271
Synthesis of 3,4-dihydrobenzo[g]isoquinoline-1(2H)-ones and 3,4-dihydroisoquinoline-1(2H)-ones skeleton via intramolecular electrophilic cyclization
272
Synthesis of 3,4-Dihydropyrano[c]Chromene Derivatives Using Sulfonic Acid Functionalized Silica (SiO2PrSO3H)
273
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
274
Synthesis of 3,4-dihydropyrimidin-2(1H)-ones and 1,4-dihydropyridines using ammonium carbonate in water
275
Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones Catalyzed by Nafion-H Under Ultrasound Irradiation and Solvent-Free Conditions
276
Synthesis of 3,4-dihydropyrimidin-2-ones (DHPMs) using mesoporous aluminosilicate (AlKIT-5) catalyst with cage type pore structure
277
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
278
Synthesis of 3,4-Dihydropyrimidinones using Nano γ-Al2O3/BF3/ Fe3O4 as an Efficient Magnetic Nanocatalyst under Solvent-free Conditions
279
Synthesis of 3,4-dihydropyrrolo[2,1-a]isoquinolines based on [3+2] cycloaddition initiated by Rh2(cap)4-catalyzed oxidation
280
Synthesis of 3,4-dihydroquinazolin-4-one: selenium-catalyzed reductive N-heterocyclization of N-(2-nitrobenzoyl)amides with carbon monoxide
281
Synthesis of 3,4-Dihydroquinoxalin-2-Amine, Diazepine-Tetrazole and Benzodiazepine-2-Carboxamide Derivatives with the Aid of H6P2W18O62/Pyridino-Fe3O4
282
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
283
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
284
Synthesis of 3,4-disubstituted 2(1H)-quinolinones via intramolecular Friedel–Crafts reaction of N-arylamides of Baylis–Hillman adducts
285
Synthesis of 3,4-disubstituted 2,5-dihydrofurans starting from the Baylis–Hillman adducts via consecutive radical cyclization, halolactonization, and decarboxylation strategy
286
Synthesis of 3,4-disubstituted cinnolines by the Pd-catalyzed annulation of 2-iodophenyltriazenes with an internal alkyne
287
Synthesis of 3,4-disubstituted piperidines by ene cyclisation of 4-aza-1,7-dienes
288
Synthesis of 3,4-disubstituted α-methylene-γ-lactones via sonochemical Barbier-type reaction
289
Synthesis of 3,4-fused cycloalkanopyrroles by 1,3-dipolar cycloaddition
290
Synthesis of 3,4-substituted cyclopentenones via an intramolecular Pauson–Khand reaction of NO linked enynes
291
Synthesis of 3,5,6-trisubstituted α-pyrones from Baylis–Hillman adducts
292
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
293
Synthesis of 3,5-Diaryl Azoline and [1,4] Diazepine Derivatives via Microwave Irradiation
294
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
295
Synthesis of 3,5-diazabicyclo [5.1.0] octenes. A new platform to mimic glycosidase transition states
296
Synthesis of 3,5-difunctionalized 1-methyl-1H-pyrazolo[3,4-b]pyridines involving palladium-mediated coupling reactions
297
Synthesis of 3,5-dioxoalkanoates, 3,5-dioxopimelates and 2,4-dioxoadipates by acylation of 1,3-bis-silyl enol ethers
298
Synthesis of 3,5-disubstituted 1,2,4-oxadiazoles and their behavior of liquid crystallines
299
Synthesis of 3,5-disubstituted 1,2,4-oxadiazoles as peptidomimetic building blocks
300
Synthesis of 3,5-disubstituted 1,2,4-oxadiazoles using ionic liquid-phase organic synthesis (IoLiPOS) methodology
301
Synthesis of 3,5-disubstituted-1,2,4-oxadiazoles using tetrabutylammonium fluoride as a mild and efficient catalyst
302
Synthesis of 3,5-lutidine from propionaldehyde over modified ZSM-5 catalysts Original Research Article
303
Synthesis of 3,6-bicyclolides: A novel class of macrolide antibiotics
304
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
305
Synthesis of 3,6-branched arabinogalactan-type tetra- and hexasaccharides for characterization of monoclonal antibodies Original Research Article
306
Synthesis of 3,6-branched oligomannoside fragments of the mannan from Candida albicans cell wall corresponding to the antigenic factor 4 Original Research Article
307
Synthesis of 3,6-diazabicyclo[3.1.1]heptanes as novel ligands for neuronal nicotinic acetylcholine receptors
308
Synthesis of 3,6-diazabicyclo[3.1.1]heptanes as novel ligands for the opioid receptors Original Research Article
309
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
310
Synthesis of 3,6-dioxa-Δ7-4-trifluoromethyl perfluorooctyl trifluoromethyl sulfonimide: bis[(perfluoroalkyl)sulfonyl] superacid monomer and polymer
311
Synthesis of 3,6-epoxy[1,5]dioxocines from 2-hydroxyaromatic benzaldehydes
312
Synthesis of 3,7-dihydroimidazo[1,2a]pyrazine-3-ones and their chemiluminescent properties
313
Synthesis of 3,8,13,18-tetrachloro-2,7,12,17-tetramethoxyporphyrin
314
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
315
Synthesis of 3/8-carbonylated chlorophyll derivatives and regiodependent reductivity of their carbonyl substituents
316
Synthesis of 3-[(N-carboalkoxy)ethylamino]-indazole-dione derivatives and their biological activities on human liver carbonyl reductase Original Research Article
317
Synthesis of 3-[2-(1,3-butadienyl)]-1H-indoles en route to murrapanine analogue
318
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
319
Synthesis of 3′-, 4′- and 6′-deoxy and other analogues of d-glucosaminylphosphatidylinositol
320
Synthesis of 3′,4′-epoxynoraristeromycin analogs for molecular labeling probe of S-adenosyl-l-homocysteine hydrolase Original Research Article
321
Synthesis of 3′-allylindoline spirobenzopyrans derived from 3-allyl-3H-indoles
322
Synthesis of 3′-azido-4′-ethynyl-3′,5′-dideoxy-5′-norarabinouridine: a new anti-HIV nucleoside analogue
323
Synthesis of 3′-C-substituted thymidine derivatives by free-radical techniques: scope and limitations
324
Synthesis of 3′-deoxy-3′-C-methyl nucleoside derivatives Original Research Article
325
Synthesis of 3′-deoxy-3′-C-methyl-β-d-ribonucleoside analogs
326
Synthesis of 3′-O-phosphonomethyl nucleosides with an adenine base moiety
327
Synthesis of 30 wt%BAS/Si3N4 composite by spark plasma sintering
328
Synthesis of 32-nitro-chlorophyll-a derivatives and their electronic absorption/emission data
329
Synthesis of 32-substituted bacteriochlorophyll-d analogs and their self-aggregation in a nonpolar organic solvent
330
Synthesis of 35–40 mers of RNA oligomers from unblocked monomers. A simple approach to the RNA world
331
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
332
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
333
Synthesis of 3-acetamido-1,2,4-tri-O-acetyl-3,5-dideoxy-5-C-[(R)- and (S)-phenylphosphinyl]-α- and -β-d-xylopyranoses
334
Synthesis of 3-acetonyl- and 3-(2-oxoethyl)glutarates
335
Synthesis of 3-acyltetrahydrofurans from formaldehyde acetals of allylic diols
336
Synthesis of 3-alkenyl-2-arylchromones and 2,3-dialkenylchromones via acid-catalysed retro-Michael ring opening of 3-acylchroman-4-ones
337
Synthesis of 3-alkoxycarbonyl-1β-methylcarbapenem using palladium-catalyzed amidation of vinyl halide
338
Synthesis of 3-alkyl naphthalenes as novel estrogen receptor ligands
339
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
340
Synthesis of 3-alkyl-1-isoindolinones by alkylation of a benzotriazolyl substituted N-dimethylamino-phthalimidine
341
Synthesis of 3-alkyl-5-hydroxycyclohex-2-enones via aldolic addition/sulfinate elimination tandem reactions
342
Synthesis of 3-alkylidene-piperidin-4-ones via one-pot cascade transylidation–olefination
343
Synthesis of 3-alkyloxazolidin-2,4-diones using 2-chloroacetamides, carbon dioxide and 1,8-diazabicyclo[5.4.0]undecene (DBU)
344
Synthesis of 3-amido-3-deoxy-β-d-talopyranosides: all-cis-substituted pyranosides as lectin inhibitors
345
SYNTHESIS OF 3-AMINO-1-PHENYL-1H-PYRAZOLE-4, 5-DIONE-4-ARYLHYDRAZONES AS FAST DYES
346
Synthesis of 3-amino-5H-pyrrolo[2,3-e]-1,2,4-triazines by Sonogashira/copper(I)-catalyzed heteroannulation
347
Synthesis of 3-amino-5-methyl-[1,1 -biaryl]-2,4-dicarbonitriles using ZnFe2O4 magnetic nanoparticles
348
Synthesis of 3-aminoaspartic acid derivatives from glycine precursors
349
Synthesis of 3-aminoindole derivatives: combination of Thorpe–Ziegler cyclization and unexpected allylindium-mediated decyanation
350
Synthesis of 3-aminopyrrolidines and piperidines from endocyclic enamine derivatives
351
Synthesis of 3-aminopyrrolidines by cyclization of neutral C-centered α-aminoalkyl radicals
352
Synthesis of 3-aryl substituted benzo[1,2,5]triazepin-4-ones via intramolecular imine formation
353
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
354
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
355
Synthesis of 3-aryl-4-chalcogen-2H-benzopyrans from 3-iodo-4-chalcogen-2H-benzopyrans using a Suzuki cross-coupling
356
Synthesis of 3-aryl-4-methyl-1,2-benzenedisulfonimides, new chiral Brønsted acids. A combined experimental and theoretical study
357
Synthesis of 3-arylcoumarins through N-heterocyclic carbene catalyzed condensation and annulation of 2-chloro-2-arylacetaldehydes with salicylaldehydes
358
Synthesis of 3-arylcoumarins via Suzuki-cross-coupling reactions of 3-chlorocoumarin
359
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
360
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
361
Synthesis of 3-Aryl-Substituted Tetrahydropyran-4-ones and Tetrahydrothiopyran-4-ones
362
Synthesis of 3-azabicyclo[4.1.0]heptane-1-carboxylic acid
363
Synthesis of 3-azido-3-deoxy-β-d-galactopyranosides Original Research Article
364
Synthesis of 3-benzazepines and azepino[4,5-b]heterocyclic ring systems via intramolecular Friedel–Crafts cyclization
365
Synthesis of 3-benzyl-2-substituted quinoxalines as novel monoamine oxidase A inhibitors
366
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
367
Synthesis of 3-buten-1-ol from 1,4-butanediol over indium oxide Original Research Article
368
Synthesis of 3-C-(6-O-acetyl-2,3,4-tri-O-benzyl-α-d-mannopyranosyl)-1-propene: a caveat
369
Synthesis of 3-C-(methyl β-d-xylofuranosid-3-yl)-5-phenyl-1,2,4-oxadiazole
370
Synthesis of 3-chloroanthranilates from α,γ,γ-trichloro-β-iminoesters
371
Synthesis of 3-C-Spiro Ring Nucleoside Analogues, of Possible Biological Activity
372
Synthesis of 3-cyano-2-fluoropyridines
373
Synthesis of 3-cyclohexylpropyl caffeate from 5-caffeoylquinic acid with consecutive enzymatic conversions in ionic liquid
374
Synthesis of 3D hierarchical Ag microspheres assembled with dendritic morphology
375
Synthesis of 3D hierarchical porous carbon as an electrode material for electric double layer capacitors
376
Synthesis of 3D hierarchical porous carbon as electrode material for electric double layer capacitors
377
Synthesis of 3-deaza-3-nitro-2′-deoxyadenosine Original Research Article
378
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
379
Synthesis of 3-deoxy-2-ulosonic acid KDO and 4-epi-KDN, a highly efficient approach of 3-C homologation by propargylation and oxidation
380
Synthesis of 3-deoxy-3,3-difluoro-d-ribohexose from gem-difluorohomoallyl alcohol
381
Synthesis of 3-Deoxyclarithromycin through Biotransformation of Clarithromycin by Aspergillus niger and its Antibacterial Activity
382
Synthesis of 3-derivatized pyrroles precursors polymers for functionalization with biomolecules toward biosensor devices
383
Synthesis of 3-dimensional mesoporous silica using a di-block copolymer template
384
Synthesis of 3-fluoro-2-(diethoxyphosphoryl)imidazo[1,2-a]pyridine
385
Synthesis of 3-fluorobenzoyl chloride functionalized magnetic sorbent for highly efficient enrichment of perfluorinated compounds from river water samples
386
Synthesis of 3-fluoroimidazo[1,2-a]pyrimidines and 5-fluoroimidazo[2,1-b][1,3]thiazoles via heterocyclization of (N-heteroarylimino)trifluoropyruvates
387
Synthesis of 3-functionalized 3-methylazetidines
388
Synthesis of 3-halo-2,5-disubstituted furans via CuX mediated cyclization–halogenation reactions
389
Synthesis of 3-halo-analogues of HHQ, subsequent cross-coupling and first crystal structure of Pseudomonas quinolone signal (PQS)
390
Synthesis of 3-hexuloses from 1,2:5,6-di-O-isopropylidenehexitols
391
Synthesis of 3H-labeled Efomycine M
392
Synthesis of 3H-labeled N-(3-iodoprop-2E-enyl)-2β-carbomethoxy-3β-(4-methylphenyl)nortropane (PE2I) and its interaction with mice striatal membrane fragments
393
Synthesis of 3H-spiro[benzofuran-2,1′-cyclohexane] derivatives from naturally occurring filifolinol and their classical complement pathway inhibitory activity
394
Synthesis of 3-hydroxyindolin-2-one alkaloids, (±)-donaxaridine and (±)-convolutamydines A and E, through enolization–Claisen rearrangement of 2-allyloxyindolin-3-ones
395
Synthesis of 3I-O and 2I-O-monosubstituted derivatives of per-6-azido-β-cyclodextrin—potential molecular scaffolds Original Research Article
396
Synthesis of 3-iodobenzo[b]thiophenes via iodocyclization/etherification reaction sequence
397
Synthesis of 3-iodothiophenes via iodocyclization of (Z)-thiobutenynes
398
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
399
Synthesis of 3-methoxyquinolines via cyclization of 1-isocyano-2-(2-lithio-2-methoxyethenyl)benzenes
400
Synthesis of 3-methoxy-quinoxalin-2-ones from methyl trimethoxyacetate and phenylenediamines
401
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
402
Synthesis of 3-methyl-2-cyclohexenones catalyzed by mercury(II) salts and their microwave assisted BiCl3 catalyzed aldol condensations
403
Synthesis of 3-methyl-4-arylmethylene isoxazole-5(4H)-ones by visible light in aqueous ethanol
404
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
405
Synthesis of 3-methyleneisoindolin-1-ones via palladium-catalyzed C–Cl bond cleavage and cyclocarbonylation of ortho-chloro ketimines
406
Synthesis of 3-Nitro-lH-indole-2-carboxylic Acid Ethyl Ester Derivatives from Baylis-Hillman Adducts
407
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
408
Synthesis of 3-O-acyl/3-benzylidene/3-hydrazone/3-hydrazine/17-carboxyacryloyl ester derivatives of betulinic acid as anti-angiogenic agents
409
Synthesis of 3-O-methylviridicatin analogues with improved anti-TNF-α properties
410
Synthesis of 3-O-sulfoglucuronyl lacto-N-neotetraose 2-aminoethyl glycoside and biotinylated neoglycoconjugates thereof Original Research Article
411
Synthesis of 3-oxagranatane-type alkaloid analogs from carbohydrates
412
Synthesis of 3-Oxa-guaianolides from Santonin
413
Synthesis of 3-oxo oxacycloalkenes by ring closing metathesis
414
Synthesis of 3-oxo-4-benzoyl-1-phenylsuccinimide and its reactions with 1,2- dinucleophiles
415
Synthesis of 3-oxooxa- and 3-oxoazacycloalk-4-enes by ring-closing metathesis. Application to the synthesis of an inhibitor of cathepsin K
416
Synthesis of 3-pentanone from 1-propanol over CeO2–Fe2O3 catalysts Original Research Article
417
Synthesis of 3-Phenyl-2,1-benzisoxazoles via Conversion of Diethyl α-(o-Nitroaryl)benzylphosphonates
418
Synthesis of 3-phenylnaphthalenic derivatives as new selective MT2 melatoninergic ligands Original Research Article
419
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
420
Synthesis of 3-Phenylsulfanyl-1,2-dihydronaphthalenes from Methylenecyclopropanes and Benzenethiol
421
Synthesis of 3-pyrroline via domino Heck–aza-Michael reaction
422
Synthesis of 3-pyrroline-2-ones from amino acids and an aryl amine
423
Synthesis of 3-quinolinecarboxylic acid esters from the Baylis–Hillman adducts of 2-halobenzaldehyde N-tosylimines
424
Synthesis of 3-S-alkyl-3-thio-d-glucose derivatives as new non-ionic surfactants and calcium antagonists
425
Synthesis of 3-silyl-2(5H)-furanone by rhodium-catalyzed cyclocarbonylation
426
Synthesis of 3-spiropyrrolidine-3-spirooxindoles from Baylis–Hillman adducts of chromone with azomethine ylides via [3+2] cycloaddition reaction
427
Synthesis of 3-substituted 3H-indol-3-ols by the reaction of 2-isocyanophenyl ketones with Grignard reagents
428
Synthesis of 3-substituted 8,9-didehydroazepino[4,5-b]indolines via ring expansion reaction of pyrroloindolines
429
Synthesis of 3-substituted 8-hydroxy-3,4-dihydroisocoumarins via successive lateral and ortho-lithiations of 4,4-dimethyl-2-(o-tolyl)oxazoline
430
Synthesis of 3-Substituted and 2,3-Disubstituted-4H-1,4-Benzoxazines
431
Synthesis of 3-substituted and 3,4-disubstituted pyrazolin-5-ones
432
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
433
Synthesis of 3-substituted benzo[g]isoquinoline-5,10-diones: a convenient one-pot Sonogashira coupling/iminoannulation procedure
434
Synthesis of 3-substituted carbazole derivative as a host material for deep blue phosphorescent organic light-emitting diodes
435
Synthesis of 3-substituted imidazo[1,5-a]pyridines having 1-(N-picolinamidin-2-yl) group
436
Synthesis of 3-substituted indazoles and benzoisoxazoles via Pd-catalyzed cyclization reactions: application to the synthesis of nigellicine
437
Synthesis of 3-substituted Indoles through Yonemitsu Reaction with Copper Benzene-1,3,5-tricarboxylate acid Catalyst
438
Synthesis of 3-substituted isoindolin-1-ones via a palladium-catalysed 3-component carbonylation/amination/Michael addition process
439
Synthesis of 3-substituted-4-hydroxyquinoline N-oxides from the Baylis–Hillman adducts of o-nitrobenzaldehydes
440
Synthesis of 3-sulfanylpropanols containing three consecutive stereocenters via tandem Michael–aldol reaction of enoylthioamides with acetals as key reaction
441
Synthesis of 3-trialkylsilyl pyrazoles from β-oxo acylsilanes
442
Synthesis of 3-vinyl-2,5-dihydrofuran ring system via enyne metathesis
443
Synthesis of 3Y–ZrO2 nano-powders via a W/O emulsion
444
Synthesis of 3β-(5′-d-ribityl)cholestane, a putative biological precursor for fossil 3-alkylsteranes
445
Synthesis of 3β,6α-dihydroxy-5α-cholan-23-one
446
Synthesis of 3-β-d-ribofuranosyl-1 H-pyrazole-4-carboxamide
447
Synthesis of 3-β-d-ribofuranosylpyrazole-1-carboxamide
448
Synthesis of 4- and 6-substituted nitroindoles
449
Synthesis of 4-(1-oxo-isoindoline) and 4-(5,6-dimethoxy-1-oxo-isoindoline)-substituted phenoxypropanolamines and their β1-, β2-adrenergic receptor binding studies
450
Synthesis of 4-(2-arylvinyl)-8-hydroxyquinolines via anhydrous Heck coupling reaction and the PL properties of their Al complexes
451
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
452
Synthesis of 4-(2-hydroxyaryl)-3-nitro-4H-chromenes
453
Synthesis of 4-(2-Methylthiazol-4-yl)-Hexahydroquinoline and 1,4-Dihydropyrimidin Derivatives
454
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
455
Synthesis of 4(5)-phenylimidazole-based analogues of sphingosine-1-phosphate and FTY720: Discovery of potent S1P1 receptor agonists
456
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
457
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
458
Synthesis of 4-(cyclic dialkylamino)-7-azaindoles by microwave heating of 4-halo-7-azaindoles and cyclic secondary amines
459
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
460
Synthesis of 4-(thien-2-yl)-substituted coumarins through Lewis acid catalyzed Michael addition of thiophenes to 3-benzoylcoumarins followed by oxidation
461
Synthesis of 4-(trifluoromethyl) coumarins using nano sulfated-titania as solid acid catalyst under solvent-free conditions
462
Synthesis of 4-(trifluoromethyl)isoquinolines. Influence of trifluoromethyl group on the Pictet–Gams ring closure reaction
463
Synthesis of 4-, 5-, 6-, and 7-azidotryptamines
464
Synthesis of 4-, 8-, 12-arm star-branched polybutadienes with three different chain-end functionalities using a functionalized initiator
465
Synthesis of 4,17-diazasteroid inhibitors of human 5α-reductase Original Research Article
466
Synthesis of 4,4-(arylmethylene)bis(1H-pyrazol-5-ols) via multi-component reactions by using silica-bonded sulfamic acid derivatives
467
Synthesis of 4,4-(arylmethylene)bis(1H-pyrazol-5-ols) via multi-component reactions by using silica-bonded sulfamic acid derivatives
468
Synthesis of 4,4´-(arylmethylene)bis(1H-pyrazol-5-ols) catalyzed by nanosilica supported perchloric acid in water
469
Synthesis of 4,4΄-Diaminotriphenylmethane Derivatives Using H3PW12O40 and HZSM5 Zeolite under Solvent-Free Conditions
470
Synthesis of 4,4-bis(2-hydroperoxyalkyl)pyrazolidine-3,5-diones using manganese(III)-catalyzed autoxidation
471
Synthesis of 4,4-dialkoxy-3-piperidinols. Application to the synthesis of γ-acetate dehydropipecolinonitrile
472
Synthesis of 4,4-dimethyl-3,5-bis(diphenylphosphino)cyclohexanone
473
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
474
Synthesis of 4,5-diaryl-1,2,3-benzenetricarboxylates by reaction of 4-hydroxycyclopent-2-en-1-one-2-carboxylates with dimethyl acetylenedicarboxylate
475
Synthesis of 4,5-diarylquinazolines: a system with cofacial aromatic rings. Diazines. Part 39
476
Synthesis of 4,5-difluoroimidazole
477
Synthesis of 4,5-disubstituted-3-trihalomethylisothiazoles
478
Synthesis of 4,5-fused tricyclic quinolines via an acid-promoted intramolecular Friedel–Crafts allenylation of aniline derivatives
479
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
480
Synthesis of 4,6-diamino-5-(polyhydroxyalkylamido)pyrimidines: conformation of the sugar chain
481
Synthesis of 4,6-dimethyl-tetrahydro- and hexahydro-dibenzothiophene
482
Synthesis of 4,6-disubstituted pyrimidines via Suzuki and Kumada coupling reaction of 4,6-dichloropyrimidine
483
Synthesis of 4,7-indoloquinones from indole-7-carbaldehydes by Dakin oxidation
484
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
485
Synthesis of 4,8-Diarylcinnolines and Quinazolines with Potential Applications in Nonlinear Optics. Diazines. Part 28
486
Synthesis of 4-[N-methyl-4-pyridinio]-phenolate (POMP) and negative solvatochromism of this model molecule in view of nonlinear optical applications
487
Synthesis of 4′,4′-C-diaminomethyl nucleoside derivative as a building block for constructing libraries via amide bond formation
488
Synthesis of 4′-aryl-2′,3′-dideoxynucleoside analogues
489
Synthesis of 4′-benzoyloxycordycepin from adenosine
490
Synthesis of 4′-C, 3′-O bicyclic thymidine analogues using ring closure metathesis
491
Synthesis of 4′-epi-iodo-4′-deoxy-daunorubicin, a potential cancer radiotherapeutic agent
492
Synthesis of 4′-fluoroadenosine as an inhibitor of S-adenosyl-L-homocysteine hydrolase
493
Synthesis of 4′-modified noraristeromycins to clarify the effect of the 4′-hydroxyl groups for inhibitory activity against S-adenosyl-l-homocysteine hydrolase
494
Synthesis of 4′-O-acetyl-maltose and α-d-galactopyranosyl-(1→4)-d-glucopyranose for biochemical studies of amylose biosynthesis Original Research Article
495
Synthesis of 4′-substituted 2,2′:6′,2″-terpyridines via a Mitsunobu reaction
496
Synthesis of 4′-thionucleosides by 1,3-dipolar cycloadditions of the simplest thiocarbonyl ylide with alkenes bearing electron-withdrawing groups
497
Synthesis of 4″-alkoxy avermectin derivatives using rhodium carbenoid-mediated O–H insertion reaction
498
Synthesis of 45S5 Bioglass® via a straightforward organic, nitrate-free sol–gel process
499
Synthesis of 4A zeolites from kaolin for obtaining 5A zeolites through ionic exchange for adsorption of arsenic
500
Synthesis of 4-acylpyrazolone Schiff base ligand grafted silica and selectivity in adsorption of lanthanides from aqueous solutions
501
Synthesis of 4-alkoxy-2-phenylquinoline derivatives as potent antiplatelet agents
502
Synthesis of 4-alkoxy-4-methyl- and 4-alkoxy-4-fluoromethyl-1,3-benzoxazinones
503
Synthesis of 4-alkoxycarbonyl-butenolides by uncatalyzed one-pot cyclization of 1,3-bis(silyloxy)alk-1-enes with oxalyl chloride
504
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
505
Synthesis of 4-alkyl-3-bromo-2(5H)-furanones and unsymmetrically disubstituted 3,4-dialkyl-2(5H)-furanones by palladium-catalyzed cross-coupling reactions
506
Synthesis of 4-alkyl-pyrrolidine-3-carboxylic acid stereoisomers
507
Synthesis of 4-allenyl and 4-proparyl-2-azetidinone via Zn-mediated Barbier-type reaction and Pt-catalyzed intramolecular amidation to carbapenem skeletons
508
Synthesis of 4-allylquinazolines from N-(2-cyanoaryl)amides via the In-mediated allylation of nitrile and dehydrative cyclization cascade
509
Synthesis of 4-amino-1,2,3,4-tetrahydropyridine derivatives by intramolecular nucleophilic addition of tertiary enamides to in-situ generated imines
510
Synthesis of 4-amino-3-oxo-tetrahydroazepino[3,4-b]indoles: new conformationally constrained Trp analogs
511
Synthesis of 4-amino-4,5-dideoxy-l-lyxofuranose derivatives and their evaluation as fucosidase inhibitors Original Research Article
512
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
513
Synthesis of 4-aminoguaiazulene and its δ-lactam derivatives
514
Synthesis of 4-anilinopiperidine methyl esters, intermediates in the production of carfentanil, sufentanil, and remifentanil
515
Synthesis of 4-arms hydroxy-functionalized PMMA-b-PE through combining free radical polymerization with coordination polymerization
516
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
517
Synthesis of 4-aryl-2,3-dihydropyrroles via Rh-catalyzed intramolecular hydroamino-methylation reaction
518
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
519
Synthesis of 4-Aryl-4H-Chromene Derivatives with Boric Acid: Evaluation of Their in vitro Anti-Angiogenesis Effects and Possible Mechanism of Action
520
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
521
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
522
Synthesis of 4-aryl-6-indolylpyridine-3-carbonitriles and evaluation of their antiproliferative activity
523
Synthesis of 4-Arylaminoquinazolines and 2-Aryl-4-arylaminoquinazolines from 2-Aminobenzonitrile, Anilines and Formic Acid or Benzaldehydes
524
Synthesis of 4-aryl-azetidinones via intramolecular alkylation of nucleophilic arenes using acyliminium cations
525
Synthesis of 4-arylidenecyclohexane-1,3-diones from the Baylis–Hillman acetates
526
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
527
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
528
Synthesis of 4-azacyclopent-2-enones and 5,5-dialkyl-4-azacyclopent-2-enones
529
Synthesis of 4-azepanones and heteroaromatic-fused azepines
530
Synthesis of 4-aziridino[C60]fullerene-1,8-naphthalimide (C60-NI dyads) and their photophysical properties
531
Synthesis of 4-Azo-3,5-Substituted-1,2,4-Triazole Polymers and Study of their Applications
532
Synthesis of 4b,5,10a,11-tetrahydroindeno[1,2-b]quinolin-10-ones from Baylis–Hillman adducts
533
Synthesis of 4-benzyl-3-phenylbutenolide natural products
534
Synthesis of 4-butyl-1-substituted-4H-[1,2,4]triazolo[4,3-a]quinazolin-5-ones as new class of H1-antihistaminic agents
535
Synthesis of 4-carboxy-4-pyridylpiperidines through palladium-catalyzed α-arylation of esters
536
Synthesis of 4-cyano and 4-nitrophenyl 1,6-dithio-d-manno-, l-ido- and d-glucoseptanosides possessing antithrombotic activity Original Research Article
537
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
538
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
539
Synthesis of 4-cyanophenyl 2-azido-2-deoxy- and 3-azido-3-deoxy-1,5-dithio-β-d-xylopyranosides
540
Synthesis of 4-cyanophenyl 2-deoxy-1,5-dithio-β-d-threo-pentopyranoside
541
Synthesis of 4-cyanophenyl 4-azido-4-deoxy-1,5-dithio-β-d-xylopyranoside
542
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
543
Synthesis of 4-cyanophenyl and 4-nitrophenyl 1,5-dithio-l- and -d-arabinopyranosides possessing antithrombotic activity
544
Synthesis of 4-cyanophenyl and 4-nitrophenyl 2-azido-2-deoxy-1,5-dithio-β-d-arabino- and -β-d-lyxopyranosides possessing antithrombotic activity
545
Synthesis of 4-demethoxyadriamycinone utilizing ruthenium-catalyzed oxidation of allyl acetates
546
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
547
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
548
Synthesis of 4-dialkylaminopyridine derivatives through ring-rearrangement of 3-nitro-2H-pyran-2-one acetamidines
549
Synthesis of 4-Diphosphocytidyl-2-C-Methyl-D-Erythritol 2-Phosphate and Kinetic Studies of Mycobacterium tuberculosis IspF
550
Synthesis of 4-epi-2-deoxy-2-Heq-N-acetylneuraminic acid and 2,4-dideoxy-2-Heq N-acetylneuraminic acid
551
Synthesis of 4-fluoroalkyl-substituted pyridazines from fluorinated diazodiketones
552
Synthesis of 4-functionalized aryl-3,5-diacyl-1,4-dihydropyridines
553
Synthesis of 4-functionalized terdendate pyridine-based ligands
554
Synthesis of 4H-[1,3]dithiolo[4,5-b]pyrroles through the reaction of benzoyl isothiocyanate and dialkyl acetylenedicarboxylates in the presence of Ph3P
555
Synthesis of 4-halophosphaisocoumarins via halocyclization of 2-(1-alkynyl)phenylphosphonates
556
Synthesis of 4-haloserotonin derivatives and synthesis of the toad alkaloid dehydrobufotenine
557
Synthesis of 4H-benzo[e]-1,2-selanazin-4-one derivatives: a new heterocyclic ring system
558
Synthesis of 4H-pyrano[2,3-d]pyrimidine derivatives under solvent-free conditions
559
Synthesis of 4H-pyrans catalyzed by thermol-regulated PEG1000-based ionic liquid/EM
560
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
561
Synthesis of 4-hydroxy-1-methylindole and benzo[b]thiophen-4-ol based unnatural flavonoids as new class of antimicrobial agents Original Research Article
562
Synthesis of 4-hydroxy-3-[(E)-2-(6-substituted-9H-purin-9-yl)vinyl]coumarins as lipoxygenase inhibitors
563
Synthesis of 4-hydroxy-7-dimethylamino-3-pyrazolinylcoumarins and their polarity-sensitive properties
564
Synthesis of 4-hydroxyderricin and related derivatives
565
Synthesis of 4-hydroxymethyl-2,4-methanoproline
566
Synthesis of 4-hydroxysphinganine and characterization of sphinganine hydroxylase activity in corn
567
Synthesis of 4-Methoxy-1, 3-Benzenediolylhydrazones and Evaluation of Their Anti-Platelet Aggregation Activity
568
Synthesis of 4-methoxy-1H-phenalen-1-one: a subunit related to natural phenalenone-type compounds
569
Synthesis of 4-methoxy-3,5-dinitrobenzaldehyde: a correction to supposed tele nucleophilic aromatic substitution
570
Synthesis of 4-methylcoumarin-7-yl β-d-galactofuranoside, a fluorogenic substrate for galactofuranosidase
571
Synthesis of 4-methyl-thio-phenyl-propylamine and the evaluation of its interaction with different amine oxidases Original Research Article
572
Synthesis of 4-methylumbelliferyl-β-d-glucan oligosaccharides as specific chromophoric substrates of (1 → 3),(1 → 4)-β-d-glucan 4-glucanohydrolases
573
Synthesis of 4-monofluoromethylenyl- and cis-4-monofluoromethyl-l-pyroglutamic acids via a novel dehydrofluorination
574
Synthesis of 4-N-alkyl and ribose-modified AICAR analogues on solid support
575
Synthesis of 4-nitromethylene-1,4-dihydropyrimidine derivatives as pyrimidine nucleoside analogues
576
Synthesis of 4-Nitrophenyl Sulfones and Application in the Modified Julia Olefination
577
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
578
Synthesis of 4-O- and 6-O-(2′-iodoethyl)-d-glucose
579
Synthesis of 4-O-[3-(aryl)prop-2-ynyl]-Neu5Ac2en and its 4-epi-analogs modified at C-4 by Sonogashira coupling reaction
580
Synthesis of 4-O-d-Mannopyranosyl-α-d-glucopyranosides by Intramolecular Glycosylation of 6-O-Tethered Mannosyl Donors
581
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
582
Synthesis of 4-O-glycosylated 1-deoxynojirimycin derivatives as disaccharide mimics-based inhibitors of human β-glucocerebrosidase
583
Synthesis of 4-oxepanones by the Lewis acid-promoted ring-expansion reaction of cyclopropapyranones
584
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
585
Synthesis of 4-oxo-4,7-dihydrofuro[2,3-b]pyridine-5-carboxamides with broad-spectrum human herpesvirus polymerase inhibition
586
Synthesis of 4-pentenoic and 5-hexenoic acids on polystyrene resin and their use as cleavable linkers
587
Synthesis of 4-phenoxybenzamide adenine dinucleotide as NAD analogue with inhibitory activity against enoyl-ACP reductase (InhA) of Mycobacterium tuberculosis
588
Synthesis of 4-Phenyl-4,5-dihydropyranopyrazolone Derivatives with Activated Potassium Carbonate: Evaluation of Anticancer Activity on Cancer Cell Lines and Apoptosis Mechanism
589
Synthesis of 4-phenylpyrrolidin-2-one via dynamic kinetic resolution catalyzed by ω-transaminases
590
Synthesis of 4-phosphono-β-lactams via phosphite addition to acyliminium salts
591
Synthesis of 4-Pyrazolylmethylidene-2-Oxazoline and -2-Imidazoline Derivatives
592
Synthesis of 4-pyrido-6-aryl-2-substituted amino pyrimidines as a new class of antimalarial agents Original Research Article
593
Synthesis of 4-substituted 3-(indol-3-yl)maleimides and azepines with annelated indole and maleimide nuclei
594
Synthesis of 4-substituted 4-arylpiperidines
595
Synthesis of 4-substituted and 3,4-disubstituted indazole derivatives by palladium-mediated cross-coupling reactions
596
Synthesis of 4-substituted azepino[3,4-b]indole-1,5-diones
597
Synthesis of 4-substituted homoallylic alcohols via a one-pot tandem Lewis-acid catalyzed crotylboration-[3,3]-sigmatropic rearrangement
598
Synthesis of 4-substituted phenyl 2,5-anhydro-1,6-dithio-α-d-gluco- and -α-l-guloseptanosides possessing antithrombotic activity Original Research Article
599
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
600
Synthesis of 4-Substituted Phosphacoumarins via Cross-Coupling of 4-Tosylphosphacoumarins with Organozinc Reagents
601
Synthesis of 4-substituted pyrano[4,3-b]pyran-2,5-diones in an ionic liquid
602
Synthesis of 4-substituted tetrahydropyridines by cross-coupling of enol phosphates
603
Synthesis of 4-substituted-2-acetamido-2,4-dideoxy-mannopyranoses using 1,6-anhydro sugar chemistry
604
Synthesis of 4-sulfonatooxy-2,2,6,6-tetramethylpiperidine-1-yloxyl derivatives for investigation of ionic liquids
605
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
606
Synthesis of 4-thiofuranoid 1,2-glycals and their application to stereoselective synthesis of 4′-thionucleosides
607
Synthesis of 4-thiophen-2′-yl-1,4-dihydropyridines as potentiators of the CFTR chloride channel Original Research Article
608
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
609
Synthesis of 4-trifluoromethylpyrido[1,2-a]pyrimidin-2-ones utilizing activated alkynoates
610
Synthesis of 4-trifluoromethylsteroids: A novel class of steroid 5α-reductase inhibitors
611
Synthesis of 4-trimethylammonio-2,2,6,6-tetramethylpiperidine-1-yloxyl with various anions for investigation of ionic liquids
612
Synthesis of 4-unsubstituted 2H-1,2,3-benzothiadiazine 1,1-dioxides via ortho lithiation of protected benzaldehyde derivatives
613
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
614
Synthesis of 4-unsubstituted dihydropyrimidines. Nucleophilic substitution at position-2 of dihydropyrimidines
615
Synthesis of 5- and 6-(6-Chloro-3-pyridyl)-2-azabicyclo[2.2.0]hexanes. Epibatidine Analogs
616
Synthesis of 5-(1-H or 1-alkyl-5-oxopyrrolidin-3-yl)-8-hydroxy-[1,6]-naphthyridine-7-carboxamide inhibitors of HIV-1 integrase
617
Synthesis of 5(20)deoxydocetaxel, a new active docetaxel analogue
618
Synthesis of 5-(2-amino-2-deoxy-β- -glucopyranosyloxymethyl)-2′-deoxyuridine and its incorporation into oligothymidylates
619
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
620
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
621
Synthesis of 5-(3-indolyl)oxazole natural products. Structure revision of Almazole D
622
Synthesis of 5(6)-dihydro-OSW-1 by using the intact skeleton of tigogenin
623
Synthesis of 5-(7′-indolyl)oxazoles and 2,5-di-(7′-indolyl)oxazoles
624
Synthesis of 5-(7-hydroxyhept-3-enyl)-1,2-dithiolan-3-one 1-oxide, a core functionality of antibiotic leinamycin
625
Synthesis of 5-(mercaptomethyl)-3(E)-undecene-1,11-dioic acid, a non-peptide glutathione analog
626
Synthesis of 5-(perfluoroalkylmethyl)-1,3-dioxolan-4-ones
627
Synthesis of 5-(phenylsulfanyl)-1,4-dihydropyrazine-2,3-diones via an unexpected microwave-assisted cascade reaction
628
Synthesis of 5-(sulfamoylmethyl)indoles
629
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
630
Synthesis of 5-(trifluoromethyl)cyclohexane-1,3-dione and 3-amino-5-(trifluoromethyl)cyclohex-2-en-1-one: new trifluoromethyl building block
631
Synthesis of 5-(ω-sulfhydrylalkyl)salicylaldehydes as precursors for the preparation of alkanethiol-modified metal salens
632
Synthesis of 5,10,15,20-tetrakis(2-amino-5-methoxyphenyl)-porphyrin: a versatile building block for porphyrin face selection
633
Synthesis of 5,10-diphenylporphyrin
634
Synthesis of 5,15-diarylporphyrins via orthoesters condensation with aryldipyrromethanes
635
Synthesis of 5,5,6,6,21,21,22,22-octamethyl-5,6,21,22-tetragerma[10.10]paracyclophane
636
Synthesis of 5,5′-bis-benzofurans and 5-arylbenzofurans
637
Synthesis of 5,5′-diarylated 2,2′-bithiophenes via palladium-catalyzed arylation reactions
638
Synthesis of 5,6-bis(alkyn-1-yl)pyrimidines and related nucleosides
639
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
640
Synthesis of 5,6-dihydro-2H-thiins and 2,3-dihydro-1,4-oxathiins based on 1-benzylsulfonyl-1,1-dihydropolyfluoroalkan-2-ones
641
Synthesis of 5,6-dihydro-4H-1,3-thiazine containing peptide mimics from N-(3-hydroxypropyl)thioamides and epimerization studies
642
Synthesis of 5,6-dihydro-4-hydroxy-2-pyrones via formal cycloaddition reactions
643
Synthesis of 5,6-dihydrobenz[c]acridines: a comparative study
644
Synthesis of 5,6-dihydrophenanthridines via N,O-acetal TMS ethers
645
Synthesis of 5,7,12,14-Tetraarylpentacenes from Pentacene-5,7,12,14-tetrone and Characterisation of the Tetrol Intermediates
646
Synthesis of 5,8-dimethoxy-3-hydroxy-4-quinolone, a reported inhibitor of HIV RT, and evidence the original proposed structure was incorrect
647
Synthesis of 5′,9-anhydro-3-(β-d-ribofuranosyl)xanthine, and 3,5′-anhydro-xanthosine as potential anti-hepatitis C virus agents
648
Synthesis of 5′-C-methyl-1′,3′-dioxolan-4′-yl nucleosides
649
Synthesis of 5′-functionalized adenosine: suppression of cyclonucleoside formation
650
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
651
Synthesis of 5′-seleno-xylofuranosides
652
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
653
Synthesis of 5″-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca2+-mobilizing agent: The first antagonists modified at the N1-ribose moiety
654
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
655
Synthesis of 5-Acetoxy-2(5H)-Furanones through Manganese(III)-Promoted Functionalization of Arylacetylenes
656
Synthesis of 5-acetyl-2-aminopyrrole C-deoxyribonucleoside
657
Synthesis of 5-alkoxymethyl- and 5-aminomethyl-substituted 8-hydroxyquinoline derivatives and their luminescent Al(III) complexes for OLED applications
658
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
659
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
660
Synthesis of 5-alkyl-4-amino-2-(trifluoromethyl)pyridines and their transformation into trifluoromethylated 1H-pyrazolo[4,3-c]pyridines
661
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
662
Synthesis of 5-alkylidene-2,5-dihydropyrrol-2-ones based on cyclizations of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with oxalyl chloride
663
Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles
664
Synthesis of 5-alkynylated uracil–morpholino monomers using Sonogashira coupling
665
Synthesis of 5-amino-1-aryl-4-cyanoimidazoles from formamidines under solvent-free condition
666
Synthesis of 5-amino-2-aminoalkyl-1,3-oxazol-4-ylphosphonic acid derivatives and their use in the preparation of phosphorylated peptidomimetics
667
Synthesis of 5-amino-2-selenoxo-1,3-imidazole-4-carboselenoamides by the reaction of isoselenocyanates with aminoacetonitriles
668
Synthesis of 5-aminoisoxazolines from N-allyl compounds and nitrile oxides via tandem isomerization-1,3-dipolar cycloaddition
669
Synthesis of 5-aminothiazoles as building blocks for library synthesis
670
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
671
Synthesis of 5-aryl-5′-formyl-2,2′-bithiophenes as new precursors for nonlinear optical (NLO) materials
672
Synthesis of 5-arylamino-1-arylpyrazoles from 5-aminopyrazoles with arylhalides via CuI catalyzed Ullman coupling reaction
673
Synthesis of 5-arylhistidines via a Suzuki–Miyaura cross-coupling
674
Synthesis of 5-arylidene-2-amino-4-azolones and evaluation of their anticancer activity Original Research Article
675
Synthesis of 5-arylidene-2-aryl-3-(2-chlorophenothiazinoacetamidyl)l,3-thiazolidin-4-ones as antifungal and anticonvulsant agents
676
Synthesis of 5-arylmethylene-pyrimidine-2,4,6-trione and 2-arylidenemalononitriles derivatives using a new Brønsted acid nano magnetic catalyst
677
Synthesis of 5-arylpyrrolo[2,1-c][1,4]benzodiazepines under mild cyclodehydration conditions
678
Synthesis of 5-arylthiazoles. Comparative study between Suzuki cross-coupling reaction and direct arylation
679
Synthesis of 5-aryltriazole ribonucleosides via Suzuki coupling and promoted by microwave irradiation
680
Synthesis of 5-aza-analogues of angucyclines: manipulation of the 2-deoxy-C-glycoside subunit
681
Synthesis of 5-benzoylacenaphthene in the presence of Lewis acidic ionic liquids
682
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
683
Synthesis of 5-bromo-6-methyl imidazopyrazine, 5-bromo and 5-chloro-6-methyl imidazopyridine using electron density surface maps to guide synthetic strategy
684
Synthesis of 5-chloro-N-aryl-1H-indole-2-carboxamide derivatives as inhibitors of human liver glycogen phosphorylase a Original Research Article
685
Synthesis of 5-deazaflavin derivatives and their activation of p53 in cells Original Research Article
686
Synthesis of 5-deazathiogirollines: analogs of a natural antitumor agent
687
Synthesis of 5-deoxy-5-epifluoro derivatives of arbekacin, amikacin, and 1-N-[(S)-4-amino-2-hydroxybutanoyl]tobramycin (study on structure — toxicity relationships)
688
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
689
Synthesis of 5-deoxypterocarpens, pterocarpens, and coumestans by intramolecular Heck reaction
690
Synthesis of 5-deoxy-β-d-galactofuranosides as tools for the characterization of β-d-galactofuranosidases Original Research Article
691
Synthesis of 5-endo-, 5-exo-, 6-endo- and 6-exo-hydroxylated analogues of epibatidine
692
Synthesis of 5-epiaragusterol A
693
Synthesis of 5-ethoxymethylfurfural from 5-hydroxymethylfurfural and fructose in ethanol catalyzed by MCM-41 supported phosphotungstic acid
694
Synthesis of 5-Fluorouracil nanoparticles via supercritical gas antisolvent process
695
Synthesis of 5-fluorouridine 5′-diphosphate galactose from 5-fluorouridine by chemical phosphorylation and microbial uridylyl transfer
696
Synthesis of 5-fluorovinyl derivatives of pyrimidines via Suzuki–Miyaura coupling and their 1,3-dipolar cycloaddition reactions with nitrones
697
Synthesis of 5-haloethynyl- and 5-(1,2-dihalo)vinyluracil nucleosides: Antiviral activity and cellular toxicity Original Research Article
698
Synthesis of 5-halogenated 1,2,3-triazoles under stoichiometric Cu(I)-mediated azide–alkyne cycloaddition (CuAAC or ‘Click Chemistry’) Original Research Article
699
Synthesis of 5-heteroarylazulenes: first selective electrophilic substitution at the 5-position of azulene
700
Synthesis of 5H-pyridazino[4,5-b]indoles and their benzofurane analogues utilizing an intramolecular Heck-type reaction
701
Synthesis of 5-HT3 receptor antagonists, [11C]Y-25130 and [11C]YM060
702
Synthesis of 5-Hydroxy- and 5-Amino-1-tosyl-5-phenyl-3-(2-arylvinyl)4,5-dihydropyrazoles
703
Synthesis of 5-hydroxy-2-(β-d-ribofuranosyl)pyran-4-one from a pyranulose glycoside
704
Synthesis of 5-hydroxyquinolines
705
Synthesis of 5-membered heterocycles using benzoylacetonitriles as synthon
706
Synthesis of 5-methoxylated 3-pyrrolin-2-ones via the rearrangement of chlorinated pyrrolidin-2-ones
707
Synthesis of 5-methylfuro[3,2-c]quinolin-4(5H)-one via palladium-catalysed cyclisation of N-(2-iodophenyl)-N-methyl-3-furamide
708
Synthesis of 5-nitro- and 5-aminobenzimidazolone-2
709
Synthesis of 5-O-methylembelin
710
Synthesis of 5-substituted 1H-tetrazoles catalyzed by ceric ammonium nitrate supported HY-zeolite
711
Synthesis of 5-substituted 1H-tetrazoles catalyzed by ytterbium triflate hydrate
712
Synthesis of 5-substituted 2-(4- or 3-methoxyphenyl)-4(1H)-quinolones
713
Synthesis of 5-substituted 2,3-dihydrobenzofurans in a one-pot oxidation/cyclization reaction
714
Synthesis of 5-substituted 3-mercapto-1,2,4-triazoles via Suzuki–Miyaura reaction
715
Synthesis of 5-substituted analogues of huperzine A
716
Synthesis of 5-substituted derivatives of isophthalic acid as non-polymeric amphiphilic coating for metal oxide nanoparticles
717
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
718
Synthesis of 5-substituted pipecolic acid derivatives as new conformationally constrained ornithine and arginine analogues
719
Synthesis of 5-substituted quinazolinone derivatives and their inhibitory activity in vitro
720
Synthesis of 5-Substituted-1,3,4-Oxadiazole-2(3H)-Thiones Under Microwave Irradiation
721
Synthesis of 5-substituted-3,4-dihydroxycyanopyrrolidines. An easy access to polyhydroxyprolines
722
Synthesis of 5-thio-l-altrose
723
Synthesis of 5-Thiomannose-containing oligomannoside mimics: Binding abilities to concanavalin A
724
Synthesis of 5-thioxo-6H-imidazo[1,2-c]quinazolines and related compounds based on cyclocondensations of 2-isothiocyanatobenzonitrile (ITCB) with α-aminoketones
725
Synthesis of 5-trichloromethyl-Δ4-1,2,4-oxadiazolines and their rearrangement into formamidine derivatives
726
Synthesis of 6- and 7-propargyloxy derivatives of 4-(3-fluoroanilino)-quinazoline
727
Synthesis of 6- or 4-functionalized indoles via a reductive cyclization approach and evaluation as aromatase inhibitors
728
Synthesis of 6-(2-thienyl)purine nucleoside derivatives that form unnatural base pairs with pyridin-2-one nucleosides
729
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
730
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)
731
Synthesis of 6(α,β)-aminocholestanols as ergosterol biosynthesis inhibitors
732
Synthesis of 6-, 7- and 8-membered cyclosiloxanes having multifunctional groups
733
Synthesis of 6-, 7-, and 8-membered lactones via the nickel-catalysed electrochemical arylation of electron-deficient olefins
734
Synthesis of 6,6-bisbenzannulated spiroketals related to the rubromycins using a double intramolecular hetero-Michael addition (DIHMA)
735
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
736
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
737
Synthesis of 6,7-diaza-19-norvitamin D compounds
738
Synthesis of 6,7-dichloropyrido[1,2-a]benzimidazole-8,9-dione and its analogues and their reactions with nucleophiles
739
Synthesis of 6,7-dideoxy-7-isothiocyanatoheptoses: stable fully unprotected monosaccharide isothiocyanates
740
Synthesis of 6,7-dihydro-5H-dibenzo[c,e]azepines and biaryls by palladium-catalyzed Ullmann reaction
741
Synthesis of 6,7-disubstituted-5H-pyrrolo[2,3-b]pyrazines via palladium-catalyzed heteroannulation
742
Synthesis of 6,7-ethylenedioxyquinoxalines and pyrido[2,3-b]pyrazines as intermediates in the preparation of antineoplastic agents
743
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
744
Synthesis of 6′-acylamido-6′-deoxy-α-d-galactoglycerolipids Original Research Article
745
Synthesis of 6′-deoxy-6′-fluorosucrose Original Research Article
746
Synthesis of 6′-GM2, a regioisomer of ganglioside GM2, for studying the mechanism of action of GM2 activator
747
Synthesis of 60- and 72 kDa heat shock proteins in early porcine embryogenesis
748
Synthesis of 61-bis(1-adamantylcarbamoyl)-1,2-methano[60]fullerene and its antagonistic effect on haloperidol-induced catalepsy in mice
749
Synthesis of 6-acyl-5,8-quinolinediols by photo-Friedel–Crafts acylation using sunlight
750
Synthesis of 6-Acylmethylphenanthridine Enaminones
751
Synthesis of 6a-hydroxypterocarpans via intramolecular benzoin condensation
752
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
753
Synthesis of 6-amino-1,6-anhydro-6-deoxysugar derivatives
754
Synthesis of 6-Amino-1H-Indole-4,7- Quinones
755
Synthesis of 6-amino-6-deoxyhyaluronan as an intermediate for conjugation with carboxylate-containing compounds: application to hyaluronan–camptothecin conjugates Original Research Article
756
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
757
Synthesis of 6-aryl-2,4-diamino-pyrimidines and triazines using palladium catalysed Suzuki cross-coupling reactions
758
Synthesis of 6-aryl-2′-deoxyuridine nucleosides via a Liebeskind cross-coupling methodology
759
Synthesis of 6-aryluridines via Suzuki–Miyaura cross-coupling reaction at room temperature under aerobic ligand-free conditions in neat water
760
Synthesis of 6-Aziridineyl and 6-Triazol-yl of D- Glucitol Derivatives
761
Synthesis of 6-bromo-2-arylindoles using 2-iodobenzoic acid as precursor
762
Synthesis of 6-carboxylated phenanthridines by oxidative alkoxycarbonylation–cyclization of 2-isocyanobiphenyls with carbazates
763
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
764
Synthesis of 6-cyano and 6-unsubstituted 2-aryl-8-oxopurine from a common 2-oxoimidazole precursor
765
Synthesis of 6-deoxy-5-thio-d-glucose
766
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
767
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
768
Synthesis of 6-deoxy-6-halolaminarans and conversion of 6-chloro-6-deoxylaminaran into the 6-amino-6-deoxy derivative
769
Synthesis of 6-deoxy-l-idose and l-acovenose from 1,2:5,6-di-O-isopropylidene-α-d-glucofuranose Original Research Article
770
Synthesis of 6-deoxy-N-Cbz-d,l-iminoglycal-derived vinyl epoxides and examination of their regio- and stereoselectivity in nucleophilic addition reactions
771
Synthesis of 6-ethynylpurine derivatives
772
Synthesis of 6-formyl-pyridine-2-carboxylate derivatives and their telomerase inhibitory activities
773
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
774
Synthesis of 6H-benzo[c]chromen-6-ones by cyclocondensation of 1,3-dicarbonyl compounds with 4-chloro-3-formylcoumarin
775
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
776
Synthesis of 6H-naphtho[2,3-c]chromene-7,12-diones via palladium-catalyzed intramolecular cyclization of 2-bromo-3-aryloxymethyl-1,4-naphthoquinones
777
Synthesis of 6-hydroxy-2-naphthoic acid from 2,6-diisopropylnaphthalene using NHPI as a key catalyst
778
Synthesis of 6-hydroxymethyl-5,6-dihydro-4H-1,2-oxazines by one-pot-cyclization of dilithiated oximes with epibromohydrin
779
Synthesis of 6I-amino-6I-deoxy-2I–VII,3I–VII-tetradeca-O-methyl-cyclomaltoheptaose
780
Synthesis of 6-imino-5-tetrahydro-1H-2-pyrrolylidenhexahydro-2,4-pyrimidinediones as intermediates for the synthesis of C-azanucleosides
781
Synthesis of 6-methoxy-4H-1-benzopyran-7-ol, a character donating component of the fragrance of Wisteria sinensis
782
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
783
Synthesis of 6-N-(benzothiazol-2-yl)deoxyadenosine and its exciton-coupled circular dichroism Original Research Article
784
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
785
Synthesis of 6-O-methotrexylhyaluronan as a drug delivery system Original Research Article
786
Synthesis of 6-O-methyl-azithromycin and its ketolide analogue via Beckmann rearrangement of 9(E)-6-O-methyl-erythromycin oxime
787
Synthesis of 6-oxacyclopropa[a]indene derivatives starting from Baylis–Hillman adducts via Pd-mediated C(sp3)–H activation
788
Synthesis of 6-phenyl-2,2′-bipyridine ligands bearing polyaromatic substituents
789
Synthesis of 6-substituted 1-phenylbenzazepines and their dopamine D1 receptor activities Original Research Article
790
Synthesis of 6-substituted 5-cyano-7-hydroxy-2-carboxybenzofurans
791
Synthesis of 6-substituted 7-aryl-5,6-dihydropyrido[2,3-d]pyrimidine(1H,3H)-2,4-diones using the Vilsmeier reaction
792
Synthesis of 6-substituted imidazo[2,1-b]thiazoles via Pd/Cu-mediated Sonogashira coupling in water
793
Synthesis of 6-substituted tetrahydropyridinones and cyclization to indolizidine and quinolizidine structures
794
Synthesis of 6-sulfodisaccharides by beta-N-acetylhexosaminidase-catalyzed transglycosylation
795
Synthesis of 6-thio pseudo glycolipids and their orientation on a gold slide studied by IRRAS
796
Synthesis of 6-vinyl and 5-vinylproline analogues of ascomycin
797
Synthesis of 6Z,8E-heneicosadien-11-one, a sex pheromone of the painted apple moth, Teia anartoides
798
Synthesis of 7- and 10-spermine conjugates of paclitaxel and 10-deacetyl-paclitaxel as potential prodrugs
799
Synthesis of 7-(E)-alkenyl-4-amino-3-quinolinecarbonitriles via Pd-mediated Heck, Stille, and Suzuki reactions
800
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
801
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
802
Synthesis of 7,8-disubstituted benzolactam-V8 and its binding to protein kinase C
803
Synthesis of 7,9-dideoxybaccatin IV analogs from sinenxan A
804
Synthesis of 7′-[123I]iodo-d-luciferin for in vivo studies of firefly luciferase gene expression
805
Synthesis of 7-alkoxy-4-trifluoromethylcoumarins via the von Pechmann reaction catalyzed by molecular iodine
806
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
807
Synthesis of 7-aryl-1,8-naphthyridines via addition of aryl boronic acids to 1,8-naphthyridine N-oxides
808
Synthesis of 7-azabicyclo[2.2.1]heptane derivatives via bridgehead radicals
809
Synthesis of 7-azabicyclo[2.2.1]heptane-1,4-dicarboxylic acid, a rigid non-chiral analogue of 2-aminoadipic acid
810
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
811
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
812
Synthesis of 7-chloro-4-substituted aminoquinolines and their in vitro ability to produce methemoglobin in canine hemolysate
813
Synthesis of 7-cyano- and 7-acetamido-indoles via cyanocarbonation/hydrogenation of 7-formyl indole
814
Synthesis of 7-cycloalkylimino substituted 3-amino-6-fluoro-2-methyl-3H-quinazolin-4-ones
815
Synthesis of 7-deoxycholic amides or cholanes containing distinctive ion-recognizing groups at C3 and C12 and evaluation for ion-selective ionophores
816
Synthesis of 7-hydroxy-4-methylcoumarin via the Pechmann reaction with Amberlyst ion-exchange resins as catalysts
817
Synthesis of 7-hydroxycoumarins by Pechmann reaction using Nafion resin/silica nanocomposites as catalysts
818
Synthesis of 7-membered cyclic hydroxyguanidines: Novel HIV-1 protease inhibitors
819
Synthesis of 7-methoxybenzolactam-V8 using aminomercuration as a key reaction
820
Synthesis of 7-O-(2-deoxy-2-sulfamido-α-d-glucopyranosyl)-4-methylcoumarin sodium salt: a fluorogenic substrate for sulfamidase
821
Synthesis of 7-O-galloyl-d-sedoheptulose
822
Synthesis of 7-oxa-phomopsolide E and its C-4 epimer
823
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
824
Synthesis of 7-Substituted Fluoroquinolone Derivatives Contain- ing Triazolidine Dione Moiety and In Vitro Evaluation of Their Cytotoxic Effects
825
Synthesis of 7-thiaarachidonic acid as a mechanistic probe of prostaglandin H synthase-2
826
Synthesis of 7-trifluoromethylpyrazolo[1,5-a]pyridinedicarboxylate
827
Synthesis of 7α- and 7β-spermidinylcholesterol, squalamine analogues
828
Synthesis of 7α-methoxy-2-(1,3-dithiolan-2-ylidene)cephem sulphones. A new series of human leukocyte elastase inhibitors
829
Synthesis of 7α-substituted androstenediones by a 1,4-conjugate addition approach
830
Synthesis of 8-(2′-deoxy-β-d-ribofuranosyl)imidazo[1,2-a]-s-triazin-4-one
831
Synthesis of 8-(S)-methoxy-11-desmethyl laulimalide: a novel laulimalide analogue
832
Synthesis of 8,9-disubstituted fluoranthenes by domino two-fold Heck/electrocyclization/dehydrogenation of 1,2-dibromoacenaphthylene
833
Synthesis of 8-[18F]Fluoroguanine Derivatives: In Vivo Probes for Imaging Gene Expression with Positron Emission Tomography
834
Synthesis of 8-aminoadenosine 5′-(aminoalkyl phosphates), analogues of aminoacyl adenylates Original Research Article
835
Synthesis of 8-aryl substituted benzo[a]phenanthridine derivatives by consecutive three component tandem reaction and 6-endo carbocyclization
836
Synthesis of 8-arylated catechin and epicatechin derivatives via Suzuki cross-coupling
837
Synthesis of 8-arylsulfoxyl/sulfonyl adenines
838
Synthesis of 8-azidooctyl glycoside derivatives of the O-chain repeating unit of Escherichia coli O9a lipopolysaccharide and a methylated analog Original Research Article
839
Synthesis of 8-C-glucosylflavones Original Research Article
840
Synthesis of 8-chloro-benzo[c]quinolizin-3-ones as potent and selective inhibitors of human steroid 5α-reductase 1
841
Synthesis of 8-geranyloxypsoralen analogues and their evaluation as inhibitors of CYP3A4 Original Research Article
842
Synthesis of 8-hydroxyquinoline functionalised DO3A ligand and Eu(III) and Er(III) complexes: Luminescence properties
843
Synthesis of 8-O-alkylshikonin(alkannin)s: new ketal formation, tautomerism, and nucleophilic aromatic substitution
844
Synthesis of 8-oxa analogues of norcocaine endowed with interesting cocaine-like activity
845
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
846
Synthesis of 8-substituted 5H,9H-6-oxa-7-aza-benzocyclononene-10,11-dione-11-O-methyloximes, a new [1,2]-oxazonine ring system
847
Synthesis of 8-Substituted 7-Azarutaecarpines
848
Synthesis of 8-substituted bicyclo[3.2.1]octane-6-carboxylic acids and anti-convulsant properties of the corresponding amides
849
Synthesis of 8-substituted xanthines via 5,6-diaminouracils: an efficient route to A2A adenosine receptor antagonists
850
Synthesis of 8-thiabicyclo[3.2.1]oct-2-enes and their binding affinity for the dopamine and serotonin transporters
851
Synthesis of 8-vinyladenosine 5′-di- and 5′-triphosphate: evaluation of the diphosphate compound on ribonucleotide reductase
852
Synthesis of 9- and 10-membered macrolactones by selective ozonolysis of 1,4-diazaphenanthrene derivatives
853
Synthesis of 9-(2-β-C-methyl-β-d-ribofuranosyl)-6-substituted purine derivatives as inhibitors of HCV RNA replication
854
Synthesis of 9,9′-biphenanthryl-10,10′-bis(oxazoline)s and their preliminary evaluations in the Friedel–Crafts alkylations of indoles with nitroalkenes
855
Synthesis of 9-[2-O-(2-Methoxyethyl)-β-D-Ribofuranosyl]purines Using 1-Methanesulfonyloxy-2-Methoxyethane
856
Synthesis of 99mTc(CO)3-deoxyuridine derivatives as potential HSV1-tk gene expression imaging agents
857
Synthesis of 99mTc-ciprofloxacin by different methods and its biodistribution
858
Synthesis of 9-alkyl and 9-heteroalkyl substituted 2-amino-6-guanidinopurines and their influence on the NO-production in macrophages Original Research Article
859
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
860
Synthesis of 9-anthrylmethyl-functionalised cyclopentadienyl derivatives of rhodium(I) and iridium(I) and study of their luminescence properties
861
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
862
Synthesis of 9-ethynyl-9-fluorenol and its derivatives for crystallographic and optical properties study
863
Synthesis of 9H-fluoren-9-yl benzodithioates and their application as reversible addition–fragmentation chain transfer agents in living radical polymerization of styrene
864
Synthesis of 9-membered masked enediyne analogues possessing DNA intercalator and sugar moieties
865
Synthesis of 9-oxa-noradamantane derivative, an aesthetically pleasing ‘oxa-basket’
866
Synthesis of 9-oxime-11,12-carbamate ketolides Through a novel N-deamination reaction of 11,12-hydrazonocarbamate ketolide Original Research Article
867
Synthesis of 9-oxiranyl-9H-purine derivatives in β-cyclodextrin cavity
868
Synthesis of 9-substituted tetrahydrodiazepinopurines—asmarine A analogues
869
Synthesis of 9-substituted xanthenes by the condensation of arynes with ortho-hydroxychalcones
870
Synthesis of a (+)-anatoxin-a analogue for monoclonal antibodies production
871
Synthesis of a (B12H11S)2− containing glucuronoside as potential prodrug for BNCT
872
Synthesis of a (piperazin-1-ylmethyl)biaryl library via microwave-mediated Suzuki–Miyaura cross-couplings
873
Synthesis of a (thienylethenyl)benzimidazole platinum acetylide complex
874
Synthesis of a (β-acetamido-α-acetoxyethyl)boronic ester via azido boronic esters
875
Synthesis of a [18F]labeled chelidonine derivative as a possible antitumor agent
876
Synthesis of a [2]benzazepine analogue of clavizepine
877
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
878
Synthesis of a [3.3]biphenylophane, and its photophysical and photochemical properties studied by emission and transient absorption measurements
879
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
880
Synthesis of a ‘direct-linked’ C-disaccharide from a pyranulose glycoside
881
Synthesis of a ‘twisted’ transition-state analogue of biotin
882
Synthesis of a 1,3,4,5-tetrahydrobenzindole β-ketoester
883
Synthesis of a 1,3,5-benzotriazepine-2,4-dione based library
884
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
885
Synthesis of a 10-membered ring with eleutheside functionality by Nozaki–Hiyama–Kishi coupling
886
Synthesis of a 13C,15N labeled imidazole and characterization of the 2,5-endoperoxide and its decomposition
887
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
888
Synthesis of a 188Re-HEDP complex using carrier-free 188Re, and a study of its stability
889
Synthesis of a 1α-amino-1-deoxy analogue of forskolin
890
Synthesis of a 1α-C-methyl analogue of 25-hydroxyvitamin D3: interaction with a mutant vitamin D receptor Arg274Leu
891
Synthesis of a 200-member library of squaric acid N-hydroxylamide amides
892
Synthesis of a 2-benzocymantrenylpyridine and further mechanistic insights
893
Synthesis of a 2-indolylphosphonamide derivative with inhibitory activity against yersiniabactin biosynthesis
894
Synthesis of a 3′-naphthamido-LacNAc fluorescein conjugate with high selectivity and affinity for galectin-3 Original Research Article
895
Synthesis of a 3-aminopiperidin-2,5-dione as a conformationally constrained surrogate of the Ala-Gly dipeptide
896
Synthesis of a 3-deoxy-l-iduronic acid containing heparin pentasaccharide to probe the conformation of the antithrombin III binding sequence Original Research Article
897
Synthesis of a 4′,4′-spirothietane-2′, N3-cycloadenosine as a highly constrained analogue of 5′-deoxy-5′-methylthioadenosine (MTA)
898
Synthesis of a 5-alkoxypyrido[3,4-d]pyrimidin-4(3H)-one derivative via directed ortho-metallation of a pyridine analogue
899
Synthesis of a 5-alkoxypyrido[4,3-d]pyrimidin-4(3H)-one derivative via a regioselective Meisenheimer N-oxide rearrangement
900
Synthesis of a 6V-sulfated mannopentasaccharide analogue related to PI-88 Original Research Article
901
Synthesis of a Ag–AgBiTe hybrid nano-segmented structure by a galvanic displacement reaction
902
Synthesis of a benzothiadiazole/thiophene-based oligomer for bulk heterojunction photovoltaic cells
903
Synthesis of a benzotriazole azo dye phosphoramidite for labelling of oligonucleotides
904
Synthesis of a benzotriazole phosphoramidite for attachment of oligonucleotides to metal surfaces
905
Synthesis of a benzyl-protected analog of arenarioside, a trisaccharide phenylpropanoid glycoside Original Research Article
906
Synthesis of a BF2 complex of indol-2-yl-isoindol-1-ylidene-amine: a fully conjugated azadipyrromethene
907
Synthesis of a bicontinuous electrically conductive nanocomposite via in-situ formation of RuO2 nanoparticles
908
Synthesis of a bicyclic analog of l-iduronic acid adopting the biologically relevant 2S0 conformation Original Research Article
909
Synthesis of a bicyclic double-headed nucleoside
910
Synthesis of a bicyclo[5.3.1]undecene by a facile domino enyne cross-metathesis/IMDA
911
Synthesis of a bifunctional hapten designed to mimic both transition state and to induce “bait and switch” catalysis
912
Synthesis of a binuclear copper(II) compound and its use as a copper source for preparation of an environmental catalyst
913
Synthesis of a bio-based polyamidoamine-epichlorohydrin resin and its application for soy-based adhesives
914
Synthesis of a Biochemically Important Aldehyde, 3,4-Dihydroxyphenylacetaldehyde
915
Synthesis of a Biochemically Important Aldehyde, 3,4-Dihydroxyphenylglycolaldehyde
916
Synthesis of a biocompatible gelatin functionalized graphene nanosheets and its application for drug delivery
917
Synthesis of a biocompatible polymer using siloxane-based surfactants in supercritical carbon dioxide
918
Synthesis of a biologically active isomer of kotalanol, a naturally occurring glucosidase inhibitor Original Research Article
919
Synthesis of a bioprobe for elucidation of target molecule of spongean anti-malarial peroxides
920
Synthesis of a biotinated amphiphile
921
Synthesis of a biotin-conjugate of phosmidosine O-ethyl ester as a G1 arrest antitumor drug Original Research Article
922
Synthesis of a biotin-tagged photoaffinity probe of 2-azetidinone cholesterol absorption inhibitors Original Research Article
923
Synthesis of a biotinylated camptothecin derivative and determination of the binding sequence by T7 phage display technology
924
Synthesis of a biphenyl library for studies of hydrogen bonding in the solid state
925
Synthesis of a biphenyl-based axially chiral amino acid as a highly efficient catalyst for the direct asymmetric aldol reaction
926
Synthesis of a biphenyl-based cyclophane via benzidine rearrangement of a constrained m-nitrophenol derivative
927
Synthesis of a bipyridine-derived achiral thiourea trifluoromethanesulfonic acid salt and its application as an additive in organocatalytic asymmetric reactions
928
Synthesis of a bis(diketiminate)bromosamarium(III) complex and its activity in the polymerization of methyl methacrylate Original Research Article
929
Synthesis of a bis-(N-sec-butyl-dithiocarbamato)-nitrido-99mTc complex: a potential new radiopharmaceutical for brain perfusion studies
930
Synthesis of a bis(phenoxyketimine) palladium(II) complex and its activity in the Suzuki–Miyaura reaction
931
Synthesis of a bis-azido analogue of acromelic acid for radioisotope-free photoaffinity labeling and biochemical studies
932
Synthesis of a bi-structured hybrid in a CaO–SiO2-PTMO system and in vitro evaluation on its potential of bone-bonding property
933
Synthesis of a bis-vinylogous chlorin possessing a fused naphthalene ring
934
Synthesis of a boron analogue of glucose-conjugated nucleoside diphosphate: nucleoside α-P-boranodiphosphoglucose
935
Synthesis of a boron analogue of glucose-conjugated nucleoside diphosphate: nucleoside α-P-boranodiphosphoglucose
936
Synthesis of a boron analogue of glucose-conjugated nucleoside diphosphate: nucleoside α-P-boranodiphosphoglucose
937
Synthesis of a boronated amino acid as a potential neutron therapy agent: 1-amino-3-[(dihydroxyboryl)ethyl]cyclobutanecarboxylic acid
938
Synthesis of a boron-containing conducting polymer from the anodic oxidation of Tris(pyrrolyl)borane
939
Synthesis of a branched chain aza-C-disaccharide via the cycloaddition of a chiral nitrone to an alkene, both sugar derivatives
940
Synthesis of a bromotyrosine-derived natural product inhibitor of mycothiol-S-conjugate amidase
941
Synthesis of a building block for phosphonate analogues of moenomycin A12 from d-tartaric acid
942
Synthesis of a building block for phosphonate analogues of moenomycin A12 from d-tartaric acid
943
Synthesis of a C(4)–C(9) eleutheside template from d-glucal
944
Synthesis of a C1 symmetric BINOL–terpyridine ligand and highly enantioselective methyl propiolate addition to aromatic aldehydes
945
Synthesis of a C1–C9 fragment of rhizoxin
946
Synthesis of a C1-symmetric Box macrocycle and studies towards active-template synthesis of mechanically planar chiral rotaxanes
947
Synthesis of a C3-symmetric (1→6)-N-acetyl-β-d-glucosamine octadecasaccharide using click chemistry Original Research Article
948
Synthesis of a C3-symmetric ferrocenylphosphine and its application to the Suzuki reaction of aryl chlorides
949
Synthesis of a C3-symmetric macrocycle with alternating sugar amino acid and tyrosine residues
950
Synthesis of a C8 oxygenated pyranonaphthoquinone: a useful precursor to dimeric pyranonaphthoquinones
951
Synthesis of a caged glutamate for efficient one- and two-photon photorelease on living cells
952
Synthesis of a cam system for the measurement and follow rest of multi-step shaft necks at machining
953
Synthesis of a carbamide-based dithiocarbamate chelator for the removal of heavy metal ions from aqueous solutions
954
Synthesis of a carbon monolith with trimodal pores
955
Synthesis of a carbon nanofiber/carbon foam composite from coal liquefaction residue for the separation of oil and water Original Research Article
956
Synthesis of a carbon nanotube monolith with controlled macroscopic shape
957
Synthesis of a carbon replica of zeolite Y with large crystallite size
958
Synthesis of a carbon-14 analogue of 8-chloro-11-(4-methyl-1-piperazinyl)-11-[14C]-dibenz[b,f][1,4]oxazepine
959
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
960
Synthesis of a carbon-coated NiO/MgO core/shell nanocomposite as a Pd electro-catalyst support for ethanol oxidation
961
Synthesis of a carboxyl linker containing Pk trisaccharide Original Research Article
962
Synthesis of a carotenobenzoporphyrin from a meso-diphenylporphyrin
963
Synthesis of a caryophyllene isoprenologue, a potential diterpene natural product
964
Synthesis of a cationic pyridoxamine conjugation reagent and application to the mechanistic analysis of an artificial transaminase
965
Synthesis of a cell-permeable analogue of a glycosylphosphatidylinositol (GPI) intermediate that is toxic to the living bloodstream form of Trypanosoma brucei
966
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
967
Synthesis of a C-galactopyranosyl-linked N-substituted 1,2-ethylenediamine
968
Synthesis of a C-glucosylated cyclopropylamide and evaluation as a glycogen phosphorylase inhibitor
969
Synthesis of a C-glycosylpyranonaphthoquinone related to medermycin
970
Synthesis of a chemiluminescent probe useful for the purification of steroid 5α-reductase
971
Synthesis of a chiral alcohol using a rationally designed Saccharomyces cerevisiae reductase and a NADH cofactor regeneration system
972
Synthesis of a chiral micelle-like dendrimer with phenylene dendrons and a 1,1′-binaphthyl core
973
Synthesis of a chiral steroid ring D precursor starting from carvone
974
Synthesis of a chitin-based biocomposite for water treatment: Optimization for fluoride removal
975
Synthesis of a chitosan derivative soluble at neutral pH and gellable by freeze–thawing, and its application in wound care
976
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
977
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
978
Synthesis of a chitosan-linked calix[4]arene chelating polymer and its sorption ability toward heavy metals and dichromate anions
979
Synthesis of a chlorogenin glycoside library using an orthogonal protecting group strategy Original Research Article
980
Synthesis of a chlorothalonil peptide conjugate mimicking protein-bound pesticide residues
981
Synthesis of a cholestane glycoside OSW-1 with potent cytostatic activity Original Research Article
982
Synthesis of a cholesterol-appended Tb–DTPA complex by combined removal of tert-Butyl protecting groups and complexation of terbium(III)
983
Synthesis of a class of new phosphine-oxazoline ligands and their applications in palladium-catalyzed asymmetric addition of arylboronic acids to isatins Original Research Article
984
Synthesis of a C-linked hyaluronic acid disaccharide mimetic Original Research Article
985
Synthesis of a clinoptilolite–Fe system with high Cu sorption capacity Original Research Article
986
Synthesis of a COMC–estradiol conjugate for targeted, tissue-selective cancer chemotherapy
987
Synthesis of a common key intermediate for (−)-tetrodotoxin and its analogs
988
Synthesis of a common trisaccharide fragment of glycoforms of the outer core region of the Pseudomonas aeruginosa lipopolysaccharide
989
Synthesis of a complementary dimer from mono(imidazolyl)-substituted cobalt(II) porphyrin as a new artificial T-form hemoglobin
990
Synthesis of a complete set of contracted graphs for planar non-fractionated simple-jointed kinematic chains with all possible DOFs
991
Synthesis of a complete set of l-difluorophenylalanines, l-(F2)Phe, as molecular explorers for the CH/π interaction between peptide ligand and receptor
992
Synthesis of a complex disaccharide precursor of phosphonate analogues of the antibiotic moenomycin A12
993
Synthesis of a composite consisting of carbon nanotubes and graphite shell-encapsulated cobalt nanoparticles using plasma-enhanced chemical vapor deposition
994
Synthesis of a compound having the essential structural unit for the hetisine-type of aconite alkaloids
995
Synthesis of a conformationally constrained threonine–valine dipeptide mimetic: design of a potential inhibitor of plasminogen activator inhibitor-1
996
Synthesis of a conformationally constrained tyrosine–glycine dipeptide mimetic: design of a potential substrate of Syk kinase
997
Synthesis of a conformationally restricted dipeptide analogue and its evaluation as a β-turn mimic
998
Synthesis of a conformationally restricted polyoxygenated crownophane
999
Synthesis of a constrained polyfunctional bicyclic iminocyclitol scaffold from l-sorbose via a tandem sequence including stereoselective intramolecular Huisgen cycloaddition
1000
Synthesis of a constrained tricyclic scaffold based on trans-4-hydroxy-l-proline
