Issue 1, 2005
From the journal:

Chemical Communications

Synthesis of cyclopropanesvia organoiron methodology: preparation of the C9–C16 alkenylcyclopropane segment of ambruticin†

Julie M. Lukesha  and  William A. Donaldson*a  

* Corresponding authors

a Department of Chemistry, Marquette University, P.O. Box 1881, Milwaukee, WI, USA
E-mail: william.donaldson@marquette.edu
Fax: 414-288-7066
Tel: 414-288-7374

Abstract

A synthesis of the C9–C16 segment of ambruticin is described which relies on organoiron methodology to establish the 1,2,3-trisubstituted cyclopropane ring.

Graphical abstract: Synthesis of cyclopropanes via organoiron methodology: preparation of the C9–C16 alkenylcyclopropane segment of ambruticin

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B413129K
Article type
Communication
Submitted
26 Aug 2004
Accepted
07 Oct 2004
First published
23 Nov 2004

Chem. Commun., 2005, 110-112

Permissions

Request permissions

Synthesis of cyclopropanes via organoiron methodology: preparation of the C9–C16 alkenylcyclopropane segment of ambruticin

J. M. Lukesh and W. A. Donaldson, Chem. Commun., 2005, 110 DOI: 10.1039/B413129K

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