Add to ORKGA variety of amines undergo Michael-type additions to α,β-unsaturated nitriles, carboxylic ester and ketones in a neat mixture without any solvent and catalyst to produce the corresponding β-amino derivatives in excellent yields
A new method for the preparation of the adducts of aromatic hetero nucleophiles (NH, SH, ОH) to the ...
Dimethyl maleate was found to be a very reactive and selective acceptor for the aza-Michael addition...
Several aliphatic nitro compounds have been employed as stabilized carbanions in the conjugate addit...
A variety of amines undergo Michael-type additions to α,β-unsaturated nitriles, carboxylic ester and...
Melamine Trisulfonic Acid (MTSA) on Neutral Alumina is used as an efficient catalyst for aza-Michael...
Conjugate addition of heteroatom nucleophiles to carbon−carbon double bonds conjugated with a strong...
Conjugate addition of heteroatom nucleophiles to carbon-carbon double bonds conjugated with a stron...
A variety of primary and secondary amines give the conjugate reaction with beta-nitroacrylates, via ...
Aliphatic and aromatic amines under go nucleophilic addition to α-β unsaturated ketone under ...
The authors thank the Royal Society for a University Research Fellowship (ADS), The Carnegie Trust f...
—Synthesis of some novel 3-alkylated indoles via an uncatalyzed Michael addition of indoles using th...
Various aminoalkyl substituted triazines have been synthesised and their activity as organocatalyst ...
Abstract The first Mukaiyama-Michael vinylogous reaction of a dioxinone-derived silyl...
Asymmetric Michael addition of β-keto esters with trans-β-nitroolefins using chiral amino amide orga...
(S)-Binam-L-prolinamide (20 mol%) catalyze the enantioselective Michael addition of several α-alkoxy...
A new method for the preparation of the adducts of aromatic hetero nucleophiles (NH, SH, ОH) to the ...
Dimethyl maleate was found to be a very reactive and selective acceptor for the aza-Michael addition...
Several aliphatic nitro compounds have been employed as stabilized carbanions in the conjugate addit...
A variety of amines undergo Michael-type additions to α,β-unsaturated nitriles, carboxylic ester and...
Melamine Trisulfonic Acid (MTSA) on Neutral Alumina is used as an efficient catalyst for aza-Michael...
Conjugate addition of heteroatom nucleophiles to carbon−carbon double bonds conjugated with a strong...
Conjugate addition of heteroatom nucleophiles to carbon-carbon double bonds conjugated with a stron...
A variety of primary and secondary amines give the conjugate reaction with beta-nitroacrylates, via ...
Aliphatic and aromatic amines under go nucleophilic addition to α-β unsaturated ketone under ...
The authors thank the Royal Society for a University Research Fellowship (ADS), The Carnegie Trust f...
—Synthesis of some novel 3-alkylated indoles via an uncatalyzed Michael addition of indoles using th...
Various aminoalkyl substituted triazines have been synthesised and their activity as organocatalyst ...
Abstract The first Mukaiyama-Michael vinylogous reaction of a dioxinone-derived silyl...
Asymmetric Michael addition of β-keto esters with trans-β-nitroolefins using chiral amino amide orga...
(S)-Binam-L-prolinamide (20 mol%) catalyze the enantioselective Michael addition of several α-alkoxy...
A new method for the preparation of the adducts of aromatic hetero nucleophiles (NH, SH, ОH) to the ...
Dimethyl maleate was found to be a very reactive and selective acceptor for the aza-Michael addition...
Several aliphatic nitro compounds have been employed as stabilized carbanions in the conjugate addit...