Synlett 1997; 1997(11): 1306-1308
DOI: 10.1055/s-1997-1004
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Asymmetric Hydrogenation of α, β, and γ-Aminoketones Catalyzed by Cationic Rhodium(I){AMPP} Complexes

Marc Devocelle, Francine Agbossou* , André Mortreux
  • *Laboratoire de Chimie Organique Appliquée de l’ENSCL Lille, URA Centre National de la Recherche Scientifique 402, Université des Sciences et Technologies de Lille, BP 108, 59652 Villeneuve d’Ascq cedex, France, FAX 33 3 21 43 65 85; e-mail agbossou@pop.univ-lille1.fr.
Further Information

Publication History

Publication Date:
31 December 2000 (online)

The chiral cationic rhodium aminophosphine-phosphinite complexes 4-6 were applied successfully in the asymmetric hydrogenation of α- (7-9), β- (10, 11) and γ- (12) aminoketone hydrochloride derivatives leading to the corresponding aminoalcohols in up to 97, 93, and 92 % enantiomeric excesses for the three types of substrates respectively.

    >