Abstract- We review some applications of copper derivatives as synthetic tools: stoichiometric organocopper reagents and organomagnesium derivatives in the presence of catalytic amounts of copper salts are able to give a regioselective addition on to acetylenic substrates and to alkylate alkyl or vinyl halides, bromohydrines, their tosylates and carboxylates, and a large variety of allylic substrates
Department of Chemistry, University of Calcutta, 92, Acharya Prafulla Chandra Road, Kolkata-700 009,...
The preparation of Rieke copper by the direct reduction of lithium (2-thienylcyano)cuprate with pref...
A convenient and synthetically attractive protocol for the allylation of aldehydes using stannous ch...
Highly reactive copper was prepared by the lithium naphthalide reductions of various copper(I) salt/...
A method has been developed for producing a highly activated zero-valent copper of sufficient reacti...
The preparation of organocopper reagents by transmetalation protocols has emerged as a versatile new...
The syn addition of alkylcopper reagents to various propargyl derivatives, i.e. HCtriple bond; lengt...
The Rieke method of metal activation has been employed to generate new forms of highly reactive copp...
Halohydrins, protected as ethers, acetals or chloro-magnesium alcoholates are sequentially transform...
The preparation of organocopper reagents by transmetalation protocols has emerged as a versatile new...
The thesis is divided into two separate parts, one treating conjugate addition and the other reducti...
We have developed a copper-catalyzed substitution reaction of propargylic ammonium salts with aryl G...
Allylic alkylations and substitutions promoted by copper(l) have been studied. These reactions are v...
Although soluble catalysts have been used in organic chemistry for many years, until the 1960s they ...
Copper is one of the most efficient and attractive metals for catalysis. In addition to their availa...
Department of Chemistry, University of Calcutta, 92, Acharya Prafulla Chandra Road, Kolkata-700 009,...
The preparation of Rieke copper by the direct reduction of lithium (2-thienylcyano)cuprate with pref...
A convenient and synthetically attractive protocol for the allylation of aldehydes using stannous ch...
Highly reactive copper was prepared by the lithium naphthalide reductions of various copper(I) salt/...
A method has been developed for producing a highly activated zero-valent copper of sufficient reacti...
The preparation of organocopper reagents by transmetalation protocols has emerged as a versatile new...
The syn addition of alkylcopper reagents to various propargyl derivatives, i.e. HCtriple bond; lengt...
The Rieke method of metal activation has been employed to generate new forms of highly reactive copp...
Halohydrins, protected as ethers, acetals or chloro-magnesium alcoholates are sequentially transform...
The preparation of organocopper reagents by transmetalation protocols has emerged as a versatile new...
The thesis is divided into two separate parts, one treating conjugate addition and the other reducti...
We have developed a copper-catalyzed substitution reaction of propargylic ammonium salts with aryl G...
Allylic alkylations and substitutions promoted by copper(l) have been studied. These reactions are v...
Although soluble catalysts have been used in organic chemistry for many years, until the 1960s they ...
Copper is one of the most efficient and attractive metals for catalysis. In addition to their availa...
Department of Chemistry, University of Calcutta, 92, Acharya Prafulla Chandra Road, Kolkata-700 009,...
The preparation of Rieke copper by the direct reduction of lithium (2-thienylcyano)cuprate with pref...
A convenient and synthetically attractive protocol for the allylation of aldehydes using stannous ch...