Synlett 1996; 1996(1): 75-78
DOI: 10.1055/s-1996-5321
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.

A New Strategy for the Synthesis of Selectively Protected Spermidine and Norspermidine Derivatives

Sandrine Lemaire-Audoire, Monique Savignac, Jean-Pierre Genêt*
  • *Laboratoire de Synthèse Organique, CNRS URA 1381, Ecole Nationale Supérieure de Chimie de Paris, 11 rue Pierre et Marie Curie, 75231 Paris Cedex 05, France
Further Information

Publication History

Publication Date:
31 December 2000 (online)

The synthesis of spermidine derivatives holding three independently removable N-protecting groups has been achieved from diallylamine using the key sequence: selective palladium-catalyzed monodesallylation of diallylamines/N-alkylation.

    >