A very simple approach has been developed for conjugate addition of a variety of aliphatic and aromatic amines to electron deficient alkenes in presence tea extract at room temperature. General applicability, operational simplicity, aqueous media, mild reaction conditions, environment friendly, high yields and applications of inexpensive and easily available catalyst are the advantages of the present procedure
Studies have demonstrated how mixing primary-tertiary or secondary-tertiary amines have improved the...
Amines undergo smooth nucleophilic addition to α,β-unsaturated compounds in the presence of a cataly...
A novel, microwave-assisted method producing anilines and phenols from activated aryl halides is rep...
A very simple approach has been developed for conjugate addition of a variety of aliphatic and aroma...
Dimethyl maleate was found to be a very reactive and selective acceptor for the aza-Michael addition...
Abstract: The utilization of green chemistry techniques are dramatically reduces chemical wastes and...
Different kinds of beta -electron-withdraw group substituted ethyl dithiocarbamates (3) were prepare...
A variety of amines undergo Michael-type additions to α,β-unsaturated nitriles, carboxylic ester and...
Amines undergo smooth conjugate addition to p-quinones in H2O at ambient temperature in the absence ...
The chemoselective, conjugate addition of nitroalkanes to electron-poor alkenes, with two electron-w...
Several aliphatic nitro compounds have been employed as stabilized carbanions in the conjugate addit...
This dissertation describes studies on carbo- and amino-functionalization of alkenes using conjugate...
This dissertation covers two projects utilizing organodiol catalyzed conjugate addition. The first p...
A comparative study of various widely used methods of reductive amination is reported. Specifically,...
Homoallylic amines prepared via addition of allylsilanes often require preformed imine substrates, m...
Studies have demonstrated how mixing primary-tertiary or secondary-tertiary amines have improved the...
Amines undergo smooth nucleophilic addition to α,β-unsaturated compounds in the presence of a cataly...
A novel, microwave-assisted method producing anilines and phenols from activated aryl halides is rep...
A very simple approach has been developed for conjugate addition of a variety of aliphatic and aroma...
Dimethyl maleate was found to be a very reactive and selective acceptor for the aza-Michael addition...
Abstract: The utilization of green chemistry techniques are dramatically reduces chemical wastes and...
Different kinds of beta -electron-withdraw group substituted ethyl dithiocarbamates (3) were prepare...
A variety of amines undergo Michael-type additions to α,β-unsaturated nitriles, carboxylic ester and...
Amines undergo smooth conjugate addition to p-quinones in H2O at ambient temperature in the absence ...
The chemoselective, conjugate addition of nitroalkanes to electron-poor alkenes, with two electron-w...
Several aliphatic nitro compounds have been employed as stabilized carbanions in the conjugate addit...
This dissertation describes studies on carbo- and amino-functionalization of alkenes using conjugate...
This dissertation covers two projects utilizing organodiol catalyzed conjugate addition. The first p...
A comparative study of various widely used methods of reductive amination is reported. Specifically,...
Homoallylic amines prepared via addition of allylsilanes often require preformed imine substrates, m...
Studies have demonstrated how mixing primary-tertiary or secondary-tertiary amines have improved the...
Amines undergo smooth nucleophilic addition to α,β-unsaturated compounds in the presence of a cataly...
A novel, microwave-assisted method producing anilines and phenols from activated aryl halides is rep...