Issue 24, 2009
From the journal:

Chemical Communications

New families of enantiopure cyclohexenonecis-diol, o-quinol dimer and hydrate metabolites from dioxygenase-catalysed dihydroxylation of phenols†

Derek R. Boyd,*a   Narain D. Sharma,a   John F. Malonea  and  Christopher C. R. Allenb  

* Corresponding authors

a School of Chemistry and Chemical Engineering, Queen’s University Belfast, Belfast, UK
E-mail: dr.boyd@qub.ac.uk
Fax: +44 (0)28 90975418
Tel: +44 (0)28 90975419

b School of Biological Sciences, Queen’s University Belfast, Belfast, UK

Abstract

Toluene dioxygenase-catalysed cis-dihydroxylation of phenols has led to the discovery of new enantiopure cyclohexenonecis-diol, o-quinol dimer and phenol hydrate metabolites having synthetic potential.

Graphical abstract: New families of enantiopure cyclohexenonecis-diol, o-quinol dimer and hydrate metabolites from dioxygenase-catalysed dihydroxylation of phenols

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Article information

DOI
https://doi.org/10.1039/B905940G
Article type
Communication
Submitted
25 Mar 2009
Accepted
22 Apr 2009
First published
13 May 2009

Chem. Commun., 2009, 3633-3635

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New families of enantiopure cyclohexenonecis-diol, o-quinol dimer and hydrate metabolites from dioxygenase-catalysed dihydroxylation of phenols

D. R. Boyd, N. D. Sharma, J. F. Malone and C. C. R. Allen, Chem. Commun., 2009, 3633 DOI: 10.1039/B905940G

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