A simple and general method in the synthesis of <i>N</i>-alkoxycarbonyl ketimines derived from isatins has been described first. Generally, the enantioselective addition of 1,3-dicarbonyl compounds to this kind of ketimine affords chiral 3-amino oxindoles in high yield and excellent ee
Substituted oxindoles continue to be recognized as important compounds of interest for drug discover...
An efficient asymmetric aza-Henry reaction of isatin-derived ketimines has been achieved by using a ...
Catalyst-controlled chemoselective and enantioselective reactions of tryptophols with isatin-derived...
This review collects the recent developments in the synthesis of chiral 3-substituted 3-amino-2-oxin...
An efficient Ugi three-component reaction of a preformed chiral ketimine derived from isatin with va...
A quinine-derived thiourea organocatalyst promoted the highly enantioselective addition of naphthols...
The reactions at the C-3 carbonyl group of isatins transform them into 2-oxindole derivatives, featu...
Chiral binaphthyl-modified squaramide-catalyzed enantioselective addition of diphenyl phosphonate to...
The reactions at the C-3 carbonyl group of isatins, by nucleophilic addition or spiroannulation, tra...
A highly enantioselective synthesis of 3-amino-2-oxindoles by direct Mannich reaction between acetyl...
Chiral α-hydroxyamide L5 derived from (S)-(+)-mandelic acid catalyzes the enantioselective addition ...
Producción CientíficaEnantioenriched 3‐amino‐3‐substituted oxindoles have been obtained by addition ...
A practical and efficient method for preparation of highly enantiomerically enriched 3-cyano-3-amin...
International audienceThe asymmetric synthesis of the 3-allyl-3-hydroxyoxindole skeleton was accompl...
(Chemical Equation Presented) Addition of Grignard reagents to chiral imines derived from isatine af...
Substituted oxindoles continue to be recognized as important compounds of interest for drug discover...
An efficient asymmetric aza-Henry reaction of isatin-derived ketimines has been achieved by using a ...
Catalyst-controlled chemoselective and enantioselective reactions of tryptophols with isatin-derived...
This review collects the recent developments in the synthesis of chiral 3-substituted 3-amino-2-oxin...
An efficient Ugi three-component reaction of a preformed chiral ketimine derived from isatin with va...
A quinine-derived thiourea organocatalyst promoted the highly enantioselective addition of naphthols...
The reactions at the C-3 carbonyl group of isatins transform them into 2-oxindole derivatives, featu...
Chiral binaphthyl-modified squaramide-catalyzed enantioselective addition of diphenyl phosphonate to...
The reactions at the C-3 carbonyl group of isatins, by nucleophilic addition or spiroannulation, tra...
A highly enantioselective synthesis of 3-amino-2-oxindoles by direct Mannich reaction between acetyl...
Chiral α-hydroxyamide L5 derived from (S)-(+)-mandelic acid catalyzes the enantioselective addition ...
Producción CientíficaEnantioenriched 3‐amino‐3‐substituted oxindoles have been obtained by addition ...
A practical and efficient method for preparation of highly enantiomerically enriched 3-cyano-3-amin...
International audienceThe asymmetric synthesis of the 3-allyl-3-hydroxyoxindole skeleton was accompl...
(Chemical Equation Presented) Addition of Grignard reagents to chiral imines derived from isatine af...
Substituted oxindoles continue to be recognized as important compounds of interest for drug discover...
An efficient asymmetric aza-Henry reaction of isatin-derived ketimines has been achieved by using a ...
Catalyst-controlled chemoselective and enantioselective reactions of tryptophols with isatin-derived...