Issue 7, 2007
From the journal:

Organic & Biomolecular Chemistry

Synthesis and absolute configuration of a constitutionally-new [5.6] spiroacetal from B. tryoni (Queensland fruit fly)†

Yvonne K. Booth,a   Patricia Y. Hayes,a   Christopher J. Moore,b   Lynette K. Lambert,c   William Kitchinga  and  James J. De Voss*a  

* Corresponding authors

a Chemistry, School of Molecular and Microbial Sciences, University of Queensland, St. Lucia, Brisbane, Australia
E-mail: j.devoss@uq.edu.au
Fax: +61 (0)7 3365 4299
Tel: +61 (0)7 3365 3825

b Department of Primary Industries, Yeerongpilly, Brisbane, Australia

c Centre for Magnetic Resonance, University of Queensland, St. Lucia, Brisbane, Australia

Abstract

A novel spiroacetal, (2S,6R,8S)-2-methyl-8-ethyl-1,7-dioxaspiro[5.6]dodecane (1), has been identified from the volatile secretions of female B. tryoni by mass spectral analysis and synthesis of an authentic, enantioenriched sample.

Graphical abstract: Synthesis and absolute configuration of a constitutionally-new [5.6] spiroacetal from B. tryoni (Queensland fruit fly)

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Article information

DOI
https://doi.org/10.1039/B701833A
Article type
Paper
Submitted
06 Feb 2007
Accepted
12 Feb 2007
First published
07 Mar 2007

Org. Biomol. Chem., 2007,5, 1111-1117

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Synthesis and absolute configuration of a constitutionally-new [5.6] spiroacetal from B. tryoni (Queensland fruit fly)

Y. K. Booth, P. Y. Hayes, C. J. Moore, L. K. Lambert, W. Kitching and J. J. De Voss, Org. Biomol. Chem., 2007, 5, 1111 DOI: 10.1039/B701833A

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