Synlett 2000; 2000(2): 221-222
DOI: 10.1055/s-2000-6491
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.

Towards the Total Synthesis of Octalactin A

Guillaume Bluet* , Jean-Marc Campagne
  • *ICSN-CNRS, Avenue de la Terrasse, 91198 Gif sur Yvette, France; Fax +33 1 69 82 30 73; E-mail: Jean-Marc.Campagne@icsn.cnrs-gif.fr
Further Information

Publication History

Publication Date:
31 December 2000 (online)

In the course of a total synthesis of octalactin A, the (C1-C7) and (C8-C15) sub-units have been built up using catalytic asymmetric reactions; specifically, an asymmetric Shi epoxidation and a vinylogous Mukaiyama-aldol reaction.

    >