Issue 47, 2006

Dioxygenase-catalysed dihydroxylation of arene cis-dihydrodiols and acetonide derivatives: a new approach to the synthesis of enantiopure tetraoxygenated bioproducts from arenes

Abstract

cis-Dihydrodiols of anthracene and benz[a]anthracene, and acetonide derivatives of the cis-dihydrodiols of benzene, fluorobenzene, biphenyl and phenanthrene have been identified as substrates for dioxygenase enzymes, yielding the corresponding enantiopure arene bioproducts, bis(cis-dihydrodiol)s and cis-diol acetonides respectively.

Graphical abstract: Dioxygenase-catalysed dihydroxylation of arene cis-dihydrodiols and acetonide derivatives: a new approach to the synthesis of enantiopure tetraoxygenated bioproducts from arenes

Supplementary files

Article information

Article type
Communication
Submitted
24 Aug 2006
Accepted
12 Sep 2006
First published
05 Oct 2006

Chem. Commun., 2006, 4934-4936

Dioxygenase-catalysed dihydroxylation of arene cis-dihydrodiols and acetonide derivatives: a new approach to the synthesis of enantiopure tetraoxygenated bioproducts from arenes

D. R. Boyd, N. D. Sharma, T. Belhocine, J. F. Malone, S. McGregor and C. C. R. Allen, Chem. Commun., 2006, 4934 DOI: 10.1039/B612191H

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