Melamine Trisulfonic Acid (MTSA) on Neutral Alumina is used as an efficient catalyst for aza-Michael addition of primary and secondary aliphatic amines to a series of α,β-unsaturated carbonyl compounds and nitriles in acetonitrile to produce the corresponding β-amino derivatives in high yields. The method being simple and offers chemoselectivity, as aromatic amines were found to be unreactive
Zirconium chloride efficiently catalyzes the conjugate addition of a variety of aliphatic amines to ...
The aza-Michael addition reaction is a vital transformation for the synthesis of functionalized chir...
Amines undergo smooth nucleophilic addition to α,β-unsaturated compounds in the presence of a cataly...
Melamine Trisulfonic Acid (MTSA) on Neutral Alumina is used as an efficient catalyst for aza-Michael...
A highly efficient, inexpensive, recyclable, convenient, and green protocol for chemoselective aza-M...
Aza-Michael reactions between primary aliphatic and aromatic amines and various Michael acceptors ha...
Aza-Michael reactions between primary amines and methyl propenoate have been investigated under env...
The aza-Michael reaction is one of the most important reactions in modern organic synthesis since a ...
Aliphatic and aromatic amines under go nucleophilic addition to α-β unsaturated ketone under ...
[[abstract]]Lewis acid, Me3SiOTf, has been shown to be a promising promoter for aza-Michael reaction...
Synthesis of a new series of 5-amino-7-aryl-6-cyano-4H-pyrano[3,2-b]pyrrole derivatives has been rep...
Dimethyl maleate was found to be a very reactive and selective acceptor for the aza-Michael addition...
The goal of this research was to explore new opportunities for the atom efficient synthesis of amine...
Vinylalumination is a highly useful reaction for the preparation of functionalized allylic alcohols....
1346-1349Aza-Micheal addition of aromatic and aliphatic amines and sulfonamides to α,β-unsaturated ...
Zirconium chloride efficiently catalyzes the conjugate addition of a variety of aliphatic amines to ...
The aza-Michael addition reaction is a vital transformation for the synthesis of functionalized chir...
Amines undergo smooth nucleophilic addition to α,β-unsaturated compounds in the presence of a cataly...
Melamine Trisulfonic Acid (MTSA) on Neutral Alumina is used as an efficient catalyst for aza-Michael...
A highly efficient, inexpensive, recyclable, convenient, and green protocol for chemoselective aza-M...
Aza-Michael reactions between primary aliphatic and aromatic amines and various Michael acceptors ha...
Aza-Michael reactions between primary amines and methyl propenoate have been investigated under env...
The aza-Michael reaction is one of the most important reactions in modern organic synthesis since a ...
Aliphatic and aromatic amines under go nucleophilic addition to α-β unsaturated ketone under ...
[[abstract]]Lewis acid, Me3SiOTf, has been shown to be a promising promoter for aza-Michael reaction...
Synthesis of a new series of 5-amino-7-aryl-6-cyano-4H-pyrano[3,2-b]pyrrole derivatives has been rep...
Dimethyl maleate was found to be a very reactive and selective acceptor for the aza-Michael addition...
The goal of this research was to explore new opportunities for the atom efficient synthesis of amine...
Vinylalumination is a highly useful reaction for the preparation of functionalized allylic alcohols....
1346-1349Aza-Micheal addition of aromatic and aliphatic amines and sulfonamides to α,β-unsaturated ...
Zirconium chloride efficiently catalyzes the conjugate addition of a variety of aliphatic amines to ...
The aza-Michael addition reaction is a vital transformation for the synthesis of functionalized chir...
Amines undergo smooth nucleophilic addition to α,β-unsaturated compounds in the presence of a cataly...