Download PDF
Synlett 1995; 1995(3): 277-279
DOI: 10.1055/s-1995-4927
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.

Synthesis of the Bicyclic Moiety of the Miharamycins by Samarium (II) Iodide Induced Ring Closure

Antony J. Fairbanks, Pierre Sinaÿ*
  • *Ecole Normale Supérieure, Département de Chimie, associé au CNRS, 24 rue Lhomond, 75231 Paris Cedex 05, France
Further Information

Publication History

Publication Date:
31 December 2000 (online)

  PDF Download  Permissions and Reprints All articles of this category

The bicyclic carbohydrate moiety of miharamycins (A and B) was constructed through intramolecular reductive cyclisation of a ketosugar with an appropriate ethynic appendage.

Miharamycins - Samarium (II) Iodide - Radical Cyclisation

      >