Dimethyl maleate was found to be a very reactive and selective acceptor for the aza-Michael addition in comparison to other commonly used electron-deficient alkenes. It reacts efficiently with a variety of aliphatic amines in complete absence of any catalyst and solvent at room temperature. Under these environmentally-friendly conditions, high yields of selectively mono-adducts were obtained within short reaction times
A very simple approach has been developed for conjugate addition of a variety of aliphatic and aroma...
The rate of Michael addition of primary amines to acrylates under different initial conditions was i...
We present a study on sequential conjugate addition of Grignard reagents to alkenyl-heteroarenes fol...
Dimethyl maleate was found to be a very reactive and selective acceptor for the aza-Michael addition...
Aza-Michael reactions between primary amines and methyl propenoate have been investigated under env...
Aza-Michael reactions between primary aliphatic and aromatic amines and various Michael acceptors ha...
The aza-Michael reaction is one of the most important reactions in modern organic synthesis since a ...
The addition of amines to conjugated alkenes has been carried out in water at room temperature very ...
Melamine Trisulfonic Acid (MTSA) on Neutral Alumina is used as an efficient catalyst for aza-Michael...
The aza-Michael addition is a versatile reaction for the modification of α,β-unsaturated carbonyl co...
International audienceAn aza-Michael addition between a maleimide and amines is described in which t...
A variety of amines undergo Michael-type additions to α,β-unsaturated nitriles, carboxylic ester and...
Dimethylcarbonate (DMC), an environmentally friendly substitute for dimethylsulfate and methyl halid...
Microwave-induced fast addition of several amines to conjugated carbonyl compounds has been carried ...
A new method for the preparation of the adducts of aromatic hetero nucleophiles (NH, SH, ОH) to the ...
A very simple approach has been developed for conjugate addition of a variety of aliphatic and aroma...
The rate of Michael addition of primary amines to acrylates under different initial conditions was i...
We present a study on sequential conjugate addition of Grignard reagents to alkenyl-heteroarenes fol...
Dimethyl maleate was found to be a very reactive and selective acceptor for the aza-Michael addition...
Aza-Michael reactions between primary amines and methyl propenoate have been investigated under env...
Aza-Michael reactions between primary aliphatic and aromatic amines and various Michael acceptors ha...
The aza-Michael reaction is one of the most important reactions in modern organic synthesis since a ...
The addition of amines to conjugated alkenes has been carried out in water at room temperature very ...
Melamine Trisulfonic Acid (MTSA) on Neutral Alumina is used as an efficient catalyst for aza-Michael...
The aza-Michael addition is a versatile reaction for the modification of α,β-unsaturated carbonyl co...
International audienceAn aza-Michael addition between a maleimide and amines is described in which t...
A variety of amines undergo Michael-type additions to α,β-unsaturated nitriles, carboxylic ester and...
Dimethylcarbonate (DMC), an environmentally friendly substitute for dimethylsulfate and methyl halid...
Microwave-induced fast addition of several amines to conjugated carbonyl compounds has been carried ...
A new method for the preparation of the adducts of aromatic hetero nucleophiles (NH, SH, ОH) to the ...
A very simple approach has been developed for conjugate addition of a variety of aliphatic and aroma...
The rate of Michael addition of primary amines to acrylates under different initial conditions was i...
We present a study on sequential conjugate addition of Grignard reagents to alkenyl-heteroarenes fol...