A new method for the preparation of the adducts of aromatic hetero nucleophiles (NH, SH, ОH) to the activated C=C bond of N-aryl-substituted maleimides using Michael reaction was developed. A possibility to obtain mono-adducts was demonstrated for 2-aminopyridine derivatives. It was proven that in the case of amino phenols, which possess three potential nucleophilic centers, only the addition to amino group occurs. Utility of the method for the formation of C–C bond in Michael reaction was also demonstrate
Thia-Michael addition reactions are significant for organic syntheses of important class of compound...
A series of N-arylmaleimides (N-aryl-MI) and N-aryl-2,3-dimethylmaleimides (N-aryl-DiMeMI) were prep...
The intramolecular hetero-Michael addition is one of the most convergent strategies for the synthesi...
We have studied the asymmetric Michael-addition of aldehydes to maleimides using optically pure 1,2-...
A primary amine-salicylamide derived from chiral trans-cyclohexane-1,2-diamine was used as an organo...
Several b-substituted alanines are synthesised in high yields by a Michael addition of nucleophiles ...
Along this PhD work, we have reported that the unique combination of hexafluoroisopropanol (HFIP), e...
The aza-Michael reaction is one of the most important reactions in modern organic synthesis since a ...
Enantiomerically pure mono-N-Boc-protected trans-cyclohexa-1,2-diamines are used as organocatalysts ...
This manuscript reviews the possibilities offered by 2,5-dimethylfuran-protected maleimides. Suitabl...
Palladium-catalysed enantioselective additions of aromatic amines to α,β-unsaturated N-imides are re...
International audienceA simple metal-free, step-economic and selective access to pyr- idines from re...
Au cours de cette thèse, nous avons rapporté que la combinaison unique de l'hexafluoroisopropanol (H...
Asymmetric Michael additions of isobutyraldehyde to maleimides catalyzed by optically pure diamines ...
Thia-Michael addition reactions are significant for organic syntheses of important class of compound...
A series of N-arylmaleimides (N-aryl-MI) and N-aryl-2,3-dimethylmaleimides (N-aryl-DiMeMI) were prep...
The intramolecular hetero-Michael addition is one of the most convergent strategies for the synthesi...
We have studied the asymmetric Michael-addition of aldehydes to maleimides using optically pure 1,2-...
A primary amine-salicylamide derived from chiral trans-cyclohexane-1,2-diamine was used as an organo...
Several b-substituted alanines are synthesised in high yields by a Michael addition of nucleophiles ...
Along this PhD work, we have reported that the unique combination of hexafluoroisopropanol (HFIP), e...
The aza-Michael reaction is one of the most important reactions in modern organic synthesis since a ...
Enantiomerically pure mono-N-Boc-protected trans-cyclohexa-1,2-diamines are used as organocatalysts ...
This manuscript reviews the possibilities offered by 2,5-dimethylfuran-protected maleimides. Suitabl...
Palladium-catalysed enantioselective additions of aromatic amines to α,β-unsaturated N-imides are re...
International audienceA simple metal-free, step-economic and selective access to pyr- idines from re...
Au cours de cette thèse, nous avons rapporté que la combinaison unique de l'hexafluoroisopropanol (H...
Asymmetric Michael additions of isobutyraldehyde to maleimides catalyzed by optically pure diamines ...
Thia-Michael addition reactions are significant for organic syntheses of important class of compound...
A series of N-arylmaleimides (N-aryl-MI) and N-aryl-2,3-dimethylmaleimides (N-aryl-DiMeMI) were prep...
The intramolecular hetero-Michael addition is one of the most convergent strategies for the synthesi...