The copper(I)-catalyzed azide–alkyne cycloaddition reaction has been extensively studied and widely applied in organic synthesis. However, the formation of 1,2,3-triazoles with electron-deficient azide has been a challenging problem. In this report, we have demonstrated the formation of regioselective 1,4-disubstituted 1,2,3-triazoles from various types of aryl terminal alkynes and azidoformates, which are electron-deficient azides, using a commercialized [Cu(CH<sub>3</sub>CN)<sub>4</sub>]PF<sub>6</sub> copper(I) catalyst under mild conditions
Silver acetylides and organic azides react under copper(i) catalysis to afford 1,4-disubstituted 1,2...
Copper(II) carboxylates are reduced efficiently by methanol in the presence of alkynes and form yell...
3-Azidoquinoline-2,4(1H,3H)-diones 1, which are readily available from 4-hydroxyquinolin-2(1H)-ones ...
The copper(I)-catalyzed azide–alkyne cycloaddition reaction has been extensively studied and widely...
The copper(I)-catalyzed azide-alkyne cycloaddition reaction has been extensively studied and widely ...
Electron deficient azides are challenging substrates in CuAAC reactions. Particularly, when N-carbo...
A copper-catalyzed azide–alkyne cycloaddition (CuAAC) reaction for the synthesis of 1,4-disubstitute...
A copper(I)-catalyzed tandem CuAAC/alkynylation reaction of various alkynes, organic azides, and br...
We report a copper-catalyzed cycloaddition of hydrogen azide (hydrazoic acid, HN$_3$) with terminal ...
Successful copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reactions may be achieved by sever...
1,4-Disubstituted-1,2,3-triazoles were obtained in excellent yields from azides and terminal alkynes...
A one-pot protocol for the synthesis of 1,2,3-triazoles has been developed starting from inactivated...
International audienceAluminotriazoles are obtained in a fully chemo‐ and regioselective manner by a...
The copper(I) catalyzed azide-alkyne cycloaddition (CuAAC) is the premier example of a click reactio...
A copper-catalyzed three-component reaction of methyl ketones, organic azides, and various one-carbo...
Silver acetylides and organic azides react under copper(i) catalysis to afford 1,4-disubstituted 1,2...
Copper(II) carboxylates are reduced efficiently by methanol in the presence of alkynes and form yell...
3-Azidoquinoline-2,4(1H,3H)-diones 1, which are readily available from 4-hydroxyquinolin-2(1H)-ones ...
The copper(I)-catalyzed azide–alkyne cycloaddition reaction has been extensively studied and widely...
The copper(I)-catalyzed azide-alkyne cycloaddition reaction has been extensively studied and widely ...
Electron deficient azides are challenging substrates in CuAAC reactions. Particularly, when N-carbo...
A copper-catalyzed azide–alkyne cycloaddition (CuAAC) reaction for the synthesis of 1,4-disubstitute...
A copper(I)-catalyzed tandem CuAAC/alkynylation reaction of various alkynes, organic azides, and br...
We report a copper-catalyzed cycloaddition of hydrogen azide (hydrazoic acid, HN$_3$) with terminal ...
Successful copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reactions may be achieved by sever...
1,4-Disubstituted-1,2,3-triazoles were obtained in excellent yields from azides and terminal alkynes...
A one-pot protocol for the synthesis of 1,2,3-triazoles has been developed starting from inactivated...
International audienceAluminotriazoles are obtained in a fully chemo‐ and regioselective manner by a...
The copper(I) catalyzed azide-alkyne cycloaddition (CuAAC) is the premier example of a click reactio...
A copper-catalyzed three-component reaction of methyl ketones, organic azides, and various one-carbo...
Silver acetylides and organic azides react under copper(i) catalysis to afford 1,4-disubstituted 1,2...
Copper(II) carboxylates are reduced efficiently by methanol in the presence of alkynes and form yell...
3-Azidoquinoline-2,4(1H,3H)-diones 1, which are readily available from 4-hydroxyquinolin-2(1H)-ones ...