Description  Claims  Drawing  Cited references 

US7375234B   [0006] 
US7763736B2   [0007] 
WO2012021390A   [0013] 
WO2009038685A   [0013] 

Library of 1,4-Disubstituted 1,2,3-Triazole Analogs of Oxazolidinone RNA-Binding Agents   [0015] 
Anisotropy studies of tRNA-T box antiterminator RNA complex in the presence of 1 ,4-disubstituted 1 ,2,3-triazoles   [0016] 
J. Für Prakt. Chemie.   [0062] 
Kinetics and Mechanism of 1,3-Dipolr Cycloadditions   [0062] 
1,3-Dipolar Cycloadditions. Past and Future   [0062] 
Click Chemistry: Diverse Chemical Function from a Few Good Reactions   [0062] 
Peptidotriazoles: Copper (I)-catalyzed 1, 3-dipolar cycloadditions on solid-phase   [0062] 
A Stepwise Huisgen Cycloaddition Process: Copper(1)-Catalyzed Regioselective ''Ligation'' of Azides and Terminal Alkynes   [0062] 
Cu-catalyzed azide-alkyne cycloaddition.   [0062] 
Ruthenium-catalyzed cycloaddition of alkynes and organic azides   [0062] 
Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism   [0062] 
Keynote review: Medicinal chemistry strategies to CB1 cannabinoid receptor antagonists   [0062] 
Click chemistry reactions in medicinal chemistry: applications of the 1,3-dipolar cycloaddition between azides and alkynes   [0062] 
The growing impact of click chemistry on drug discovery   [0062] 
Click chemistry, a powerful tool for pharmaceutical sciences   [0062] 
Click chemistry for drug development and diverse chemical-biology applications   [0062] 
''Click'' Chemistry in Polymer and Materials Science   [0062] 
''Click''chemistry in polymer and material science: an update   [0062] 
Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides   [0062] 
''Click'' Cycloadditions from a Mechanistic and Synthetic Perspective   [0062] 
Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper(I) acetylides   [0062] 
Electronic spectra and chemical reactivity   [0062] 
Multivalent neoglycoconjugates by regiospecific cycloaddition of alkynes and azides using organic-soluble copper catalysts   [0062] 
Structurally Diverse Dendritic Libraries:   A Highly Efficient Functionalization Approach Using Click Chemistry   [0062] 
Efficiency and fidelity in a click-chemistry route to triazole dendrimers by the copper(I)-catalyzed ligation of azides and alkynes   [0062] 
Highly active copper-catalysts for azide-alkyne cycloaddition   [0062] 
(NHC) CuI (NHC = N-Heterocyclic carbene) complexes as efficient catalysts for the reduction of carbonyl compounds   [0062] 
[(NHC)2Cu]X complexes as efficient catalysts for azide-alkyne click chemistry at low catalyst loadings   [0062] 
(NHC)copper(I)-catalyzed [3+2] cycloaddition of azides and Mono- Or disubstituted alkynes   [0062] 
Well-defined copper(i) complexes for Click azide-alkyne cycloaddition reactions: one Click beyond   [0062] 
A [(NHC)CuCl] complex as a latent Click catalyst   [0062] 
Catalyst Performance in “Click” Coupling Reactions of Polymers Prepared by ATRP:  Ligand and Metal Effects   [0062] 
Polytriazoles as copper(I)-stabilizing ligands in catalysis   [0062] 
A highly active catalyst for Huisgen 1,3-dipolar cycloadditions based on the tris(triazolyl)methanol-Cu(I) structure   [0062] 
Covalently immobilized tris(triazolyl)methanol-Cu(i) complexes: highly active and recyclable catalysts for CuAAC reactions   [0062] 
2-Ethynylpyridine-Promoted Rapid Copper(I) Chloride Catalyzed Azide-Alkyne Cycloaddition Reaction in Water   [0062]