A unique approach to asymmetric synthesis of various optically pure multisubstituted 2,3-dihydropyrroles catalyzed by a novel rosin-derived tertiary amine-thiourea via a tandem Michael/cyclization sequence with high yield (up to 97%) and good to excellent enantioselectivities (up to 97% ee) is present. This strategy provides an efficient and convenient method to access enantioenrich nitrogen heterocycles.Department of Applied Biology and Chemical Technolog
The scope of dihydropyranone and dihydropyridinone products accessible by isothiourea-catalysed proc...
An unprecedented organocatalytic highly enantioselective approach to a 3,4-dihydro-2<i>H</i>-thiopyr...
An enantioselective cascade Michael–Michael reaction between chalcones enolates and nitromethane cat...
A new class of dehydroabietic amine-substituted primary amine-thiourea bifunctional catalysts were d...
International audienceThe asymmetric synthesis of enantiopure pyrrolidines is reported via a streaml...
High on the list of challenges in organic chemistry is the development of new efficient chiral catal...
Reported is a new and efficient strategy for rapid construction of the chiral tetrahydropyrrolo[2,1-...
(Chemical Equation Presented) Chiral multifunctionalized pyrrolines have been synthesized by a ruthe...
International audienceOOrganocatalyzed enantioselective consecutive Michael addition of diethyl glut...
A simple chiral diamine catalyst (<b>1a</b>) was successfully applied in the asymmetric Michael reac...
A highly efficient one-pot process via a tandem reaction of catalytic asymmetric hydrogenation and o...
The first catalytic asymmetric construction of the biologically important hexahydrocoumarin scaffold...
ABSTRACT: The highly enantioselective preparation of trisubstituted pyrrolidine derivatives employin...
The stereoselective synthesis of trisubstituted 2-trifluoromethyl pyrrolidines by asymmetric Michael...
The bifunctional organocatalyst C3 <i>N</i>,<i>N</i>′-dioxide has been successfully applied to the a...
The scope of dihydropyranone and dihydropyridinone products accessible by isothiourea-catalysed proc...
An unprecedented organocatalytic highly enantioselective approach to a 3,4-dihydro-2<i>H</i>-thiopyr...
An enantioselective cascade Michael–Michael reaction between chalcones enolates and nitromethane cat...
A new class of dehydroabietic amine-substituted primary amine-thiourea bifunctional catalysts were d...
International audienceThe asymmetric synthesis of enantiopure pyrrolidines is reported via a streaml...
High on the list of challenges in organic chemistry is the development of new efficient chiral catal...
Reported is a new and efficient strategy for rapid construction of the chiral tetrahydropyrrolo[2,1-...
(Chemical Equation Presented) Chiral multifunctionalized pyrrolines have been synthesized by a ruthe...
International audienceOOrganocatalyzed enantioselective consecutive Michael addition of diethyl glut...
A simple chiral diamine catalyst (<b>1a</b>) was successfully applied in the asymmetric Michael reac...
A highly efficient one-pot process via a tandem reaction of catalytic asymmetric hydrogenation and o...
The first catalytic asymmetric construction of the biologically important hexahydrocoumarin scaffold...
ABSTRACT: The highly enantioselective preparation of trisubstituted pyrrolidine derivatives employin...
The stereoselective synthesis of trisubstituted 2-trifluoromethyl pyrrolidines by asymmetric Michael...
The bifunctional organocatalyst C3 <i>N</i>,<i>N</i>′-dioxide has been successfully applied to the a...
The scope of dihydropyranone and dihydropyridinone products accessible by isothiourea-catalysed proc...
An unprecedented organocatalytic highly enantioselective approach to a 3,4-dihydro-2<i>H</i>-thiopyr...
An enantioselective cascade Michael–Michael reaction between chalcones enolates and nitromethane cat...