Issue 11, 2003

An enantioselective double Diels–Alder approach to the tetracyclic framework of colombiasin A

Abstract

The complex tetracyclic carbon skeleton of colombiasin A is conveniently accessed through an enantioselective intermolecular Diels–Alder–sulfoxide elimination–intramolecular Diels–Alder (DA–E–IMDA) sequence.

Graphical abstract: An enantioselective double Diels–Alder approach to the tetracyclic framework of colombiasin A

Supplementary files

Article information

Article type
Communication
Submitted
06 Mar 2003
Accepted
01 May 2003
First published
13 May 2003

Org. Biomol. Chem., 2003,1, 1842-1844

An enantioselective double Diels–Alder approach to the tetracyclic framework of colombiasin A

J. H. Chaplin, A. J. Edwards and B. L. Flynn, Org. Biomol. Chem., 2003, 1, 1842 DOI: 10.1039/B302522E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements