Issue 15, 2004
From the journal:

Organic & Biomolecular Chemistry

Enantioselective synthesis of the dioxabicyclo[3.2.1]octane core of the zaragozic acids via intramolecular Wacker-type cyclisation reactions

Patrick Perlmutter,*a   Walailak Selajererna  and  Filisaty Vounatsosa  

* Corresponding authors

a School of Chemistry, Monash University, PO Box 23, 3800, Australia
E-mail: Patrick.Perlmutter@sci.monash.edu.au
Fax: (+61 3) 9905 4597
Tel: (+61 3) 9905 4522

Abstract

Wacker-type cyclisation reactions provide an effective entry into the dioxabicyclo[3.2.1]octane core of the zaragozic acid analogues.

Graphical abstract: Enantioselective synthesis of the dioxabicyclo[3.2.1]octane core of the zaragozic acids via intramolecular Wacker-type cyclisation reactions

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Article information

DOI
https://doi.org/10.1039/B406280A
Article type
Paper
Submitted
26 Apr 2004
Accepted
03 Jun 2004
First published
13 Jul 2004

Org. Biomol. Chem., 2004,2, 2220-2228

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Enantioselective synthesis of the dioxabicyclo[3.2.1]octane core of the zaragozic acids via intramolecular Wacker-type cyclisation reactions

P. Perlmutter, W. Selajerern and F. Vounatsos, Org. Biomol. Chem., 2004, 2, 2220 DOI: 10.1039/B406280A

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