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Au/Ag-Cocatalyzed aldoximes to amides rearrangement under solvent- and acid-free conditions
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[(NHC)CuX] complexes : synthesis, characterization and catalytic activities in reduction reactions and Click Chemistry : on the advantage of using well-defined catalytic systems
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N-Heterocyclic carbenes in late transition metal catalysis
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Synthesis of (+/-)-1,2,3-triazolo-4'-hydroxymethyl carbanucleosides
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Synthesis of (+/-)-1,2,3-triazolo-3'-deoxy-4'-hydroxymethyl carbanucleosides via 'click' cycloaddition
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Toxicity of copper(I)-NHC complexes against human tumor cells : induction of cell cycle arrest, apoptosis, and DNA cleavage
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Copper, silver, and gold complexes in hydrosilylation reactions
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N-heterocyclic carbene-copper complexes : synthesis and applications in catalysis
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[(NHC)(2)Cu]X Complexes as efficient catalysts for azide-alkyne click chemistry at low catalyst loadings
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A [(NHC)CuCl] complex as a latent Click catalyst
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Synthesis and characterization of [Cu(NHC)(2)]X complexes : catalytic and mechanistic studies of hydrosilylation reactions
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Study of copper(I) catalysts for the synthesis of carbanucleosides via azide-alkyne 1,3-dipolar cycloaddition
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Transition metal-catalyzed hydrosilylation of carbonyl compounds and imines : a review
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N-heterocyclic carbene-copper(I) complexes in homogeneous catalysis
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Stereoelectronic parameters associated with N-heterocyclic carbene (NHC) ligands : a quest for understanding
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N-heterocyclic carbenes as organocatalysts
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Copper-carbene complexes as catalysts in the synthesis of functionalized styrenes and aliphatic alkenes
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N-Heterocyclic carbene copper(I)-catalyzed [3+2]-cycloaddition of azides and mono- or disubstituted alkynes
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N-Heterocyclic carbene copper(I) complexes as versatile catalysts in organic synthesis
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Catalytic activity of N-heterocyclic carbene cationic copper(I) complexes
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(NHC)copper(I)-catalyzed [3+2] cycloaddition of azides and mono- or disubstituted alkynes
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A three-component tandem reductive aldol reaction catalyzed by N-heterocyclic carbene-copper complexes
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Au-I-catalyzed tandem [3,3] rearrangement-intramolecular hydroarylation : mild and efficient formation of substituted indenes