The concept of the remote activation of reactivity was first applied in asymmetric organocatalysis. An isatin 3-phenylimine derivative acts as a donor in the thiourea catalyzed asymmetric addition to unsaturated 1,4-ketoesters, affording aza-Michael adducts in high enantiomeric purity and yield
A family of 9-amino(9-deoxy) epicinchonine derivatives, possessing a range of mono- and bidentate hy...
The 1,4-conjugate addition of nucleophiles to \u3b1,\u3b2-unsaturated carbonyl compounds represents ...
A series of new thiourea catalysts prepared from natural amino acids have been applied in organocata...
The concept of the remote activation of reactivity was first applied in asymmetric organocatalysis. ...
[EN] Isatin and its derivatives have been widely studied due to their biological activities. Recentl...
A quinine-derived thiourea organocatalyst promoted the highly enantioselective addition of naphthols...
Bifunctional amino thiourea-catalyzed asymmetric additions of several nucleophiles into electron-def...
Michael addition is an important reaction because it can be used to synthesize a wide range of natur...
A convenient and functional-group-tolerant organocatalytic asymmetric 1,4-addition of azlactones and...
Michael addition is one of the most important carbon–carbon bond formation reactions. In this study,...
A new class of Michael acceptors based on α,β-unsaturated amino acids has been prepared and applied ...
International audienceThe organocatalytic enantioselective conjugate addition of secondary β-ketoami...
A novel type of primary amine thiourea organocatalysts derived from 1,2-diaminocyclohexane and 9-ami...
A kind of simple primary amine thiourea organocatalysts was developed. And their application in asym...
The growing importance of structurally diverse and functionalized enantiomerically pure unnatural am...
A family of 9-amino(9-deoxy) epicinchonine derivatives, possessing a range of mono- and bidentate hy...
The 1,4-conjugate addition of nucleophiles to \u3b1,\u3b2-unsaturated carbonyl compounds represents ...
A series of new thiourea catalysts prepared from natural amino acids have been applied in organocata...
The concept of the remote activation of reactivity was first applied in asymmetric organocatalysis. ...
[EN] Isatin and its derivatives have been widely studied due to their biological activities. Recentl...
A quinine-derived thiourea organocatalyst promoted the highly enantioselective addition of naphthols...
Bifunctional amino thiourea-catalyzed asymmetric additions of several nucleophiles into electron-def...
Michael addition is an important reaction because it can be used to synthesize a wide range of natur...
A convenient and functional-group-tolerant organocatalytic asymmetric 1,4-addition of azlactones and...
Michael addition is one of the most important carbon–carbon bond formation reactions. In this study,...
A new class of Michael acceptors based on α,β-unsaturated amino acids has been prepared and applied ...
International audienceThe organocatalytic enantioselective conjugate addition of secondary β-ketoami...
A novel type of primary amine thiourea organocatalysts derived from 1,2-diaminocyclohexane and 9-ami...
A kind of simple primary amine thiourea organocatalysts was developed. And their application in asym...
The growing importance of structurally diverse and functionalized enantiomerically pure unnatural am...
A family of 9-amino(9-deoxy) epicinchonine derivatives, possessing a range of mono- and bidentate hy...
The 1,4-conjugate addition of nucleophiles to \u3b1,\u3b2-unsaturated carbonyl compounds represents ...
A series of new thiourea catalysts prepared from natural amino acids have been applied in organocata...
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