Intramolecular Diels-Alder Strategy in a Synthetic Approach to the ­Eleutherobin Core

Abstract An attractive intermediate in the total synthesis of eleutherobin has been synthesised. The key step of this synthesis is an ­intramolecular Diels-Alder reaction, which leads to intermediate possessing rings A and C of the eleutherobin skeleton.

Saved in:
Bibliographic Details
Published in:Synlett 2005-06, Vol.2005 (9), p.1421-1424
Main Authors: Bruyère, Hélène, Samaritani, Simona, Ballereau, Stéphanie, Tomas, Alain, Royer, Jacques
Format: Article
Language:English
Subjects:
letter
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Abstract An attractive intermediate in the total synthesis of eleutherobin has been synthesised. The key step of this synthesis is an ­intramolecular Diels-Alder reaction, which leads to intermediate possessing rings A and C of the eleutherobin skeleton.
ISSN:0936-5214
1437-2096
DOI:10.1055/s-2005-869830