Add to ORKGChiral multifunctional thiourea-phosphine catalyzed asymmetric [3 + 2] annulation of Morita–Baylis–Hillman carbonates with maleimide
A series of chiral beta-aminophosphine ligands bearing different carbon backbones and electronically...
The first phosphine-catalyzed highly enantioselective [3 + 3] cycloaddition of Morita–Baylis–Hillman...
Novel aza-michael addition-asymmetric protonation to unsaturated carboxylic acids with chiral thiour...
A highly enantioselective [3 + 2] annulation of MBH carbonates and maleimides catalyzed by chiral ph...
<div><p></p><p>New chiral ferrocenylphosphines <b>LB1</b>–<b>LB9</b> were designed and prepared thro...
anhydride opening; catalytic asymmetric Biginelli reaction; organocatalysis; sulfoximines; thiourea
The asymmetric allylic alkenylation of Morita–Baylis–Hillman (MBH) carbonates with N-itaconimides as...
The chiral phosphine-triggered electrophilic ylide intermediate for a Morita–Baylis–Hillman carbonat...
Bifunctional amino thiourea-catalyzed asymmetric additions of several nucleophiles into electron-def...
Three enantiopure fluorous thioureas featuring a free -NH2 group were synthesized by direct addition...
High on the list of challenges in organic chemistry is the development of new efficient chiral catal...
4,4-Dicyano-2-methylenebut-3-enoates are employed in the phosphine-catalyzed [3 + 2] cycloaddition w...
The asymmetric allylic alkenylation of Morita–Baylis–Hillman (MBH) carbonates with <i>N</i>-itaconim...
Continuing our research on the use of organophosphorus derivatives of aziridines in asymmetric synth...
International audienceThe goal of this review is to collect the recent developments in asymmetric or...
A series of chiral beta-aminophosphine ligands bearing different carbon backbones and electronically...
The first phosphine-catalyzed highly enantioselective [3 + 3] cycloaddition of Morita–Baylis–Hillman...
Novel aza-michael addition-asymmetric protonation to unsaturated carboxylic acids with chiral thiour...
A highly enantioselective [3 + 2] annulation of MBH carbonates and maleimides catalyzed by chiral ph...
<div><p></p><p>New chiral ferrocenylphosphines <b>LB1</b>–<b>LB9</b> were designed and prepared thro...
anhydride opening; catalytic asymmetric Biginelli reaction; organocatalysis; sulfoximines; thiourea
The asymmetric allylic alkenylation of Morita–Baylis–Hillman (MBH) carbonates with N-itaconimides as...
The chiral phosphine-triggered electrophilic ylide intermediate for a Morita–Baylis–Hillman carbonat...
Bifunctional amino thiourea-catalyzed asymmetric additions of several nucleophiles into electron-def...
Three enantiopure fluorous thioureas featuring a free -NH2 group were synthesized by direct addition...
High on the list of challenges in organic chemistry is the development of new efficient chiral catal...
4,4-Dicyano-2-methylenebut-3-enoates are employed in the phosphine-catalyzed [3 + 2] cycloaddition w...
The asymmetric allylic alkenylation of Morita–Baylis–Hillman (MBH) carbonates with <i>N</i>-itaconim...
Continuing our research on the use of organophosphorus derivatives of aziridines in asymmetric synth...
International audienceThe goal of this review is to collect the recent developments in asymmetric or...
A series of chiral beta-aminophosphine ligands bearing different carbon backbones and electronically...
The first phosphine-catalyzed highly enantioselective [3 + 3] cycloaddition of Morita–Baylis–Hillman...
Novel aza-michael addition-asymmetric protonation to unsaturated carboxylic acids with chiral thiour...