Issue 38, 2007
From the journal:

Chemical Communications

An organocatalytic approach to the core of eunicellin†

Ryan Gilmour,a   Timothy J. Prior,b   Jonathan W. Burton*ac  and  Andrew B. Holmes*ade  

* Corresponding authors

a Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, UK

b CCLRC Daresbury Laboratory, Warrington, Cheshire, UK

c Chemistry Research Laboratory, Mansfield Road, Oxford, UK
E-mail: jonathan.burton@chem.ox.ac.uk
Fax: +44 1865 285002

d School of Chemistry, Bio21 Institute, University of Melbourne, Australia
E-mail: aholmes@unimelb.edu.au
Fax: +61 3834 42384

e Department of Chemistry, Imperial College, London, UK

Abstract

A stereocontrolled synthesis of the core of eunicellin is described featuring a Claisen rearrangement and a diastereoselective organocatalytic Diels–Alder reaction as the key steps.

Graphical abstract: An organocatalytic approach to the core of eunicellin

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Article information

DOI
https://doi.org/10.1039/B709322E
Article type
Communication
Submitted
27 Jun 2007
Accepted
03 Aug 2007
First published
20 Aug 2007

Chem. Commun., 2007, 3954-3956

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An organocatalytic approach to the core of eunicellin

R. Gilmour, T. J. Prior, J. W. Burton and A. B. Holmes, Chem. Commun., 2007, 3954 DOI: 10.1039/B709322E

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