Synthesis of bicyclic oxepanes: an enantioselective approach to the western part of Shaagrockol C

Authors

  • Boudjema Menhour Université de Reims Champagne Ardennes, Institut de Chimie Moléculaire de Reims, UMR 7312, UFR Sciences, Bât 18, B.P. 1039, 51687 Reims Cedex 2, France
  • Paul Aclinou Université de Reims Champagne Ardennes, Institut de Chimie Moléculaire de Reims, UMR 7312, UFR Sciences, Bât 18, B.P. 1039, 51687 Reims Cedex 2, France
  • Jean-Pierre Pete Université de Reims Champagne Ardennes, Institut de Chimie Moléculaire de Reims, UMR 7312, UFR Sciences, Bât 18, B.P. 1039, 51687 Reims Cedex 2, France

DOI:

https://doi.org/10.13171/mjc.2.3.2013.06.04.01

Abstract

In this paper, we wish to report an efficient and flexible synthetic strategy towards the synthesis of Shaagrockol C. The strategy involves the construction of a bicyclic oxepane which possess several chiral centres. Such system is present in some complex natural products.

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Published

2013-04-06

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Organic Chemistry