Synlett 1992; 1992(9): 747-748
DOI: 10.1055/s-1992-21479
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.

Aluminum Chloride Promoted Aminolysis of Lactams

Eric Bon* , Dennis C. H. Bigg, Guy Bertrand
  • *Laboratoire de Chimie de Coordination du CNRS, 205 route de Narbonne, F-31077 Toulouse Cedex, France
Further Information

Publication History

Publication Date:
08 March 2002 (online)

Aluminum chloride effectively promotes nucleophilic ring-opening reactions of N-benzoyl-, N-pivaloyl-, or N-tert-butoxycarbonyllactams (2) with a variety of primary and secondary amines. The influence of the size of the lactam ring, the environment of the carbonyl groups, and the nature of the amine on the regioselectivity of the reaction have been studied.

    >