Issue 2, 2009

Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscula

Abstract

A bidirectional synthesis of the originally proposed structures for the natural products elatenyne and a chloroenyne from Laurencia majuscula is described along with a reassessment of the structures of the halogenated enynes based upon a 13C NMR chemical shift/structure correlation.

Graphical abstract: Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscula

Supplementary files

Additions and corrections

Article information

Article type
Paper
Submitted
27 Aug 2008
Accepted
23 Oct 2008
First published
20 Nov 2008

Org. Biomol. Chem., 2009,7, 238-252

Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscula

H. M. Sheldrake, C. Jamieson, S. I. Pascu and J. W. Burton, Org. Biomol. Chem., 2009, 7, 238 DOI: 10.1039/B814953D

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