Synlett 1991; 1991(3): 202-203
DOI: 10.1055/s-1991-20680
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.

Total Synthesis of (±)-Virantmycin and Determination of Its Stereochemistry

Yoshiki Morimoto* , Fuyuhiko Matsuda, Haruhisa Shirahama
  • *Department of Chemistry. Faculty of Science, Hokkaido University, Sapporo, 060, Japan
Further Information

Publication History

Publication Date:
07 March 2002 (online)

The stereospecific total synthesis of (±)-virantmycin (1) and its diastereomer (±)-2 were efficiently achieved, featuring an intramolecular nitrene-addition reaction as the key step, without ambiguity in the relative stereochemistry at the two chiral centers (C-2 and C-3).

    >