Issue 7, 2002
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

The use of π-allyltricarbonyliron lactone complexes in the synthesis of the resorcylic macrolides α- and β-zearalenol

Svenja Burckhardta  and  Steven V. Ley*a  

* Corresponding authors

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

Abstract

A highly stereoselective synthesis of the natural products α- and β-zearalenol 1 and 2 has been achieved using π-allyltricarbonyliron lactone complexes to control the 1,5-stereochemical relationship of the oxygen functionalities found in these resorcylic macrolides.

Graphical abstract: The use of π-allyltricarbonyliron lactone complexes in the synthesis of the resorcylic macrolides α- and β-zearalenol

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Article information

DOI
https://doi.org/10.1039/B201164F
Article type
Paper
Submitted
31 Jan 2002
Accepted
14 Feb 2002
First published
08 Mar 2002

J. Chem. Soc., Perkin Trans. 1, 2002, 874-882

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The use of π-allyltricarbonyliron lactone complexes in the synthesis of the resorcylic macrolides α- and β-zearalenol

S. Burckhardt and S. V. Ley, J. Chem. Soc., Perkin Trans. 1, 2002, 874 DOI: 10.1039/B201164F

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