The explosively-growing applications of the Cu-catalyzed Huisgen 1,3-dipolar cycloaddition reaction between organic azides and alkynes (CuAAC) have stimulated an impressive number of reports, in the last years, focusing on recoverable variants of the homogeneous or quasihomogeneous catalysts. Recent advances in the field are reviewed, with particular emphasis on systems immobilized onto polymeric organic or inorganic supports
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
Copper(II) carboxylates are reduced efficiently by methanol in the presence of alkynes and form yell...
The Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC, known as the click reaction) is an establishe...
The explosively-growing applications of the Cu-catalyzed Huisgen 1,3-dipolar cycloaddition reaction...
Abstract : The copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction is arguably the flagship...
Readily prepared copper nanoparticles were found to catalyse the 1,3-dipolar cycloaddition of azides...
The three‐coordinated homoleptic Cu(I) complex with 2,6‐dimethylphenyl isocyanide in the coordinatio...
Click chemistry is a molecular synthesis strategy based on reliable, highly selective reactions with...
1,4-Disubstituted-1,2,3-triazoles, considered as an important and useful class of heterocycles with ...
The copper(I)-catalyzed azide−alkyne cycloaddition (CuAAC) reaction is considered to be the most rep...
One-pot three-component regioselective azide-alkyne cycloadditions are central reactions for synthes...
The lack of supported versions of the tris[(1-benzyl-1H-1,2,3-triazol-4-yl)methyl]amine (TBTA) ligan...
The three-coordinated homoleptic Cu(I) complex with 2,6-dimethylphenyl isocyanide in the coordinatio...
Copper(I) Cu2(µ-Br)2(tBuImCH2pyCH2L)]n (L = OMe, NEt2, NHtBu) compounds supported by flexible functi...
Two complementary catalytic systems are reported for the 1,3-dipolar cycloaddition of azides and iod...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
Copper(II) carboxylates are reduced efficiently by methanol in the presence of alkynes and form yell...
The Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC, known as the click reaction) is an establishe...
The explosively-growing applications of the Cu-catalyzed Huisgen 1,3-dipolar cycloaddition reaction...
Abstract : The copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction is arguably the flagship...
Readily prepared copper nanoparticles were found to catalyse the 1,3-dipolar cycloaddition of azides...
The three‐coordinated homoleptic Cu(I) complex with 2,6‐dimethylphenyl isocyanide in the coordinatio...
Click chemistry is a molecular synthesis strategy based on reliable, highly selective reactions with...
1,4-Disubstituted-1,2,3-triazoles, considered as an important and useful class of heterocycles with ...
The copper(I)-catalyzed azide−alkyne cycloaddition (CuAAC) reaction is considered to be the most rep...
One-pot three-component regioselective azide-alkyne cycloadditions are central reactions for synthes...
The lack of supported versions of the tris[(1-benzyl-1H-1,2,3-triazol-4-yl)methyl]amine (TBTA) ligan...
The three-coordinated homoleptic Cu(I) complex with 2,6-dimethylphenyl isocyanide in the coordinatio...
Copper(I) Cu2(µ-Br)2(tBuImCH2pyCH2L)]n (L = OMe, NEt2, NHtBu) compounds supported by flexible functi...
Two complementary catalytic systems are reported for the 1,3-dipolar cycloaddition of azides and iod...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
Copper(II) carboxylates are reduced efficiently by methanol in the presence of alkynes and form yell...
The Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC, known as the click reaction) is an establishe...