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click chemistry (280) 280
huisgen cycloaddition (280) 280
chemistry, organic (241) 241
chemistry, multidisciplinary (208) 208
terminal alkynes (191) 191
huisgen 1,3-dipolar cycloaddition (190) 190
azides (164) 164
cycloaddition (144) 144
triazoles (129) 129
index medicus (127) 127
copper (121) 121
chemistry (120) 120
alkynes (113) 113
click chemistry approach (112) 112
catalysis (98) 98
azide-alkyne cycloaddition (94) 94
1,3-dipolar cycloaddition (85) 85
chemistry, inorganic & nuclear (83) 83
derivatives (80) 80
polymer science (77) 77
triazole (76) 76
catalysts (73) 73
one-pot synthesis (69) 69
polymers (66) 66
1,2,3-triazoles (65) 65
1,4-disubstituted 1,2,3-triazoles (63) 63
chemistry, medicinal (62) 62
1,3-dipolar cycloadditions (61) 61
click-chemistry (59) 59
synthesis (57) 57
tetrazoles (57) 57
analysis (56) 56
ligands (56) 56
nanoparticles (56) 56
organic chemistry (56) 56
chemistry, applied (49) 49
water (49) 49
azide (47) 47
triazoles - chemistry (47) 47
chemistry, physical (46) 46
biochemistry & molecular biology (44) 44
azides - chemistry (43) 43
complexes (43) 43
molecular structure (42) 42
regioselective synthesis (42) 42
zykloaddition (42) 42
azid (40) 40
huisgen reaction (40) 40
design (39) 39
ligation (39) 39
chemical synthesis (37) 37
alkynes - chemistry (36) 36
click reaction (36) 36
click-chemie (36) 36
organic azides (36) 36
copper nanoparticles (35) 35
solid-phase (35) 35
coordination polymers (34) 34
copper - chemistry (34) 34
analogs (33) 33
cyanides (33) 33
heterogeneous catalyst (33) 33
triazoles - chemical synthesis (32) 32
1,2,3-triazole (31) 31
humans (31) 31
polymer (31) 31
chemical sciences (30) 30
alkine (29) 29
huisgen (29) 29
nitriles (29) 29
polymerization (29) 29
efficient (28) 28
crystallography (27) 27
inhibitors (27) 27
triazol (27) 27
block-copolymers (26) 26
chemical properties (26) 26
kupfer (26) 26
transfer radical polymerization (26) 26
5-substituted 1h-tetrazoles (24) 24
catalyst (24) 24
functionalization (24) 24
ligand (24) 24
reactivity (24) 24
biological evaluation (23) 23
cyclization (23) 23
cycloaddition reaction (23) 23
efficient synthesis (23) 23
huisgen 3+2 cycloaddition (23) 23
poly (23) 23
chemical reactions (22) 22
triazoles - pharmacology (22) 22
copper compounds (21) 21
cycloadditions (21) 21
heterogeneous catalysis (21) 21
highly efficient (21) 21
in-situ (21) 21
inorganic chemistry (21) 21
one-pot (20) 20
agents (19) 19
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Chemistry : a European journal, ISSN 0947-6539, 2015, Volume 21, Issue 2, pp. 554 - 558
...] cycloaddition of azides and alkynes to give optically pure products containing succinimide‐ and triazole‐substituted quaternary carbon stereogenic centers... 
click chemistry | copper | asymmetric catalysis | azides | alkynes | Azides | Click chemistry | Copper | Asymmetric catalysis | Alkynes | HUISGEN | MECHANISM | COMPLEXES | REACTIVITY | ALDEHYDES | CHEMISTRY, MULTIDISCIPLINARY | ACYCLIC SYSTEMS | QUATERNARY STEREOGENIC CENTERS | Yuan (China) | Catalysis | Enantiomers | Triazoles | Azide | Cycloaddition | Asymmetry | Catalysts | Ligands | Carbon | Phosphines
Journal Article
Journal of Molecular Catalysis. A, Chemical, ISSN 1381-1169, 11/2014, Volume 393, pp. 56 - 61
Journal Article
Beilstein journal of organic chemistry, ISSN 1860-5397, 2013, Volume 9, Issue 1, pp. 2715 - 2750
Journal Article
Dalton transactions : an international journal of inorganic chemistry, ISSN 1477-9226, 2011, Volume 40, Issue 32, pp. 8140 - 8144
This report describes the synthesis and characterization of 1,5-bis-triphenylphosphinegold(I) 1,2,3-triazolate (3((1,5))). The synthesis of the dinuclear... 
BASIS SETS | GOLD | HUISGEN CYCLOADDITION | LIGANDS | MOLECULAR-ORBITAL METHODS | TETRAZOLATO COMPLEXES | CHEMISTRY | TERMINAL ALKYNES | STRUCTURAL-CHARACTERIZATION | SUPRAMOLECULAR STRUCTURES | CHEMISTRY, INORGANIC & NUCLEAR
Journal Article
Catalysis Science and Technology, ISSN 2044-4753, 05/2011, Volume 1, Issue 2, pp. 166 - 178
The discovery of copper(I) species as excellent catalysts for the regioselective cycloaddition reactions of azides and alkynes served as proof-of-concept of the importance of Click chemistry and opened a broad field... 
1,4-DISUBSTITUTED 1,2,3-TRIAZOLES | BLOCK-COPOLYMERS | SULFONYL AZIDES | ONE-POT SYNTHESIS | AMIDE SYNTHESIS | CATALYZED CYCLOADDITION | EFFICIENT SYNTHESIS | REGIOSELECTIVE SYNTHESIS | CHEMISTRY, PHYSICAL | TERMINAL ALKYNES | HUISGEN 1,3-DIPOLAR CYCLOADDITION | Cycloaddition | Catalysts | Ligands | Biochemistry | Transformations | Catalysis | Copper | Alkynes
Journal Article
ACS Catalysis, ISSN 2155-5435, 06/2016, Volume 6, Issue 6, pp. 3629 - 3636
...–alkyne cycloaddition (CuAAC) has become a ubiquitous molecular linking platform. Easy access to substituted 1,4-triazoles can be exploited to engender asymmetry to a myriad of potentially useful targets in high yields... 
cycloaddition | desymmetrization | copper-catalyzed | kinetic resolution | alkyne | asymmetric catalysis | azide | ORGANIC-SYNTHESIS | UPDATE 1 | HUISGEN | ENANTIOSELECTIVE ENZYMATIC DESYMMETRIZATIONS | CLICK CHEMISTRY | SOLID-PHASE | CHEMISTRY, PHYSICAL | TERMINAL ALKYNES | 1,3-DIPOLAR CYCLOADDITION | QUATERNARY OXINDOLES
Journal Article
Monatshefte für Chemie, ISSN 0026-9247, 2018, Volume 149, Issue 8, pp. 1469 - 1474
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2015, Volume 54, Issue 40, pp. 11795 - 11799
... situ cycloaddition reaction of nitrile with azide to form tetrazoles. It has been shown that metal catalysis serves to activate the cyano group in the nitrile reagent by a coordinative interaction. A key role... 
reaction mechanisms | cycloaddition | structure elucidation | tetrazoles | metal catalysis | AZIDES | MECHANISM | CHEMISTRY, MULTIDISCIPLINARY | CLICK CHEMISTRY APPROACH | LIGANDS | NITRILES | HUISGEN 1,3-DIPOLAR CYCLOADDITION | 5-SUBSTITUTED TETRAZOLES | COORDINATION POLYMERS | CYANIDES | Nitriles | Catalysis
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 05/2015, Volume 56, Issue 22, pp. 2853 - 2859
.... The click-chemistry approaches based on Huisgen’s cycloaddition reaction are particularly attractive and have received enormous attention over the last decade and a half, due to their utility in preparing compounds with diverse applications... 
1,2,3-Triazoles | Amide isosters | Regioselectivity | Metal-free cycloaddition | Click-chemistry | AZIDE-ALKYNE CYCLOADDITION | HUISGEN CYCLOADDITION | RUTHENIUM-CATALYZED CYCLOADDITION | SOLID-PHASE | CHEMISTRY, ORGANIC | 1,5-DISUBSTITUTED 1,2,3-TRIAZOLES | TERMINAL ALKYNES | IONIC LIQUID | METAL-FREE SYNTHESIS | 1,3-DIPOLAR CYCLOADDITION | REGIOSELECTIVE SYNTHESIS | Triazoles | Methods
Journal Article
Synthesis, ISSN 0039-7881, 12/2012, Volume 44, Issue 24, pp. 3722 - 3730
Journal Article