Click chemistry is a set of highly selective and efficient reactions used in organic synthesis. It's often characterized by its simplicity, reliability, and regioselectivity. Click chemistry reactions are typically used to form covalent bonds between molecules. Examples of click reactions include the Huisgen 1,3-dipolar cycloaddition, azide-alkyne cycloaddition, and thiol-ene reactions.
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C20H14BrN3O5
1,3-bis(3-(1-(4-(3-(pyrrolidin-1-yl)propanamido)phenyl)-1H-1,2,3-triazol-4-yl)phenyl)urea
prop-2-ynyl 4-sulfamoylbenzoate
TVB-2640
TPP-3
C23H32N2O5
4-(n-butyl)-1-cyclohexyl-1H-1,2,3-triazole
1-(4-azidobutyl)-4-(2-methoxyphenyl)piperazine
tricosan-11-ylmethyl 2,3-di-O-acetyl-6-O-benzoyl-β-D-glucopyranoside
C43H51N4O9P
N-(2-((1-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)phenyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)benzamide
Dichloromethane
Triethylamine
7-((1-(4-methoxybenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-4H-chromen-4-one
8-hydroxy-5-(4-cyclohex-1-enyl-1H-1,2,3-triazol-1-yl)quinoline
3-Fluorobicyclo[1.1.1]pentane-1-carboxylicacid
C54H59N3O11
C49H69FN14O11S
o-Azidobenzylbenzoat
1-(2,5-dimethoxyphenyl)-1H-benzo[d][1,2,3]triazole
(1R,2S,3r,4R,5S,6s)-6-[((1-dodecyl-1H-1,2,3-triazol-4-yl)methyl)amino]cyclohexane-1,2,3,4,5-pentaol hydrochloride
