Allylic chlorides and acetates accelerate the reaction between copper(II) perchlorate and copper metal powder to form copper(I) perchlorate which in turn is an extremely good catalyst for the activation of these substrates towards nucleophilic substitution
A convenient and synthetically attractive protocol for the allylation of aldehydes using stannous ch...
A mild method for the synthesis of allylic amines by using a mixture of copper(II)perchlorate and co...
In this thesis we are going to first discuss the application of a copper hydride system, which was p...
Allylic chlorides and acetates accelerate the reaction between copper(II) perchlorate and copper met...
Allylic alkylations and substitutions promoted by copper(l) have been studied. These reactions are v...
Allylic alcohols, acetates, carbonates and chlorides can be activated by copper(I) salts towards nuc...
Copper is one of the most efficient and attractive metals for catalysis. In addition to their availa...
A method has been developed for producing a highly activated zero-valent copper of sufficient reacti...
International audienceModern organic synthesis now requires efficient atom economical synthetic meth...
This thesis deals with the copper-catalyzed substitution of allylic substrates. In the first part of...
This mini-review discusses the rapidly growing field of asymmetric copper-catalyzed chemistry. Altho...
The Rieke method of metal activation has been employed to generate new forms of highly reactive copp...
La substitution allylique est une réaction fondamentale pour la formation de liaison C-C. L'emploi d...
This thesis describes the study of organozirconium reagents used in copper-catalyzed asymmetric synt...
A catalyst system able to perform highly enantioselective Cu-catalysed allylic alkylations with Grig...
A convenient and synthetically attractive protocol for the allylation of aldehydes using stannous ch...
A mild method for the synthesis of allylic amines by using a mixture of copper(II)perchlorate and co...
In this thesis we are going to first discuss the application of a copper hydride system, which was p...
Allylic chlorides and acetates accelerate the reaction between copper(II) perchlorate and copper met...
Allylic alkylations and substitutions promoted by copper(l) have been studied. These reactions are v...
Allylic alcohols, acetates, carbonates and chlorides can be activated by copper(I) salts towards nuc...
Copper is one of the most efficient and attractive metals for catalysis. In addition to their availa...
A method has been developed for producing a highly activated zero-valent copper of sufficient reacti...
International audienceModern organic synthesis now requires efficient atom economical synthetic meth...
This thesis deals with the copper-catalyzed substitution of allylic substrates. In the first part of...
This mini-review discusses the rapidly growing field of asymmetric copper-catalyzed chemistry. Altho...
The Rieke method of metal activation has been employed to generate new forms of highly reactive copp...
La substitution allylique est une réaction fondamentale pour la formation de liaison C-C. L'emploi d...
This thesis describes the study of organozirconium reagents used in copper-catalyzed asymmetric synt...
A catalyst system able to perform highly enantioselective Cu-catalysed allylic alkylations with Grig...
A convenient and synthetically attractive protocol for the allylation of aldehydes using stannous ch...
A mild method for the synthesis of allylic amines by using a mixture of copper(II)perchlorate and co...
In this thesis we are going to first discuss the application of a copper hydride system, which was p...