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rdf:type |
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|
lifeskim:mentions |
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pubmed:issue |
17
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|
pubmed:dateCreated |
2002-9-25
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pubmed:abstractText |
Dioxygenase-catalysed trioxygenation of alkyl phenyl sulfides and alkyl benzenes yields enantiopure cis-dihydrodiol sulfoxides and triols respectively; naphthalene cis-dihydrodiol dehydrogenase-catalysed aromatisation of these diastereoisomers gives enantiopure catechols of either configuration.
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pubmed:language |
eng
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pubmed:journal |
|
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1359-7345
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:day |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1914-5
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
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pubmed:year |
2002
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pubmed:articleTitle |
Tandem enzyme-catalysed oxidations of alkyl phenyl sulfides and alkyl benzenes: enantiocomplementary routes to chiral phenols.
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pubmed:affiliation |
School of Chemistry, Queen's University of Belfast, Belfast, UK BT9 5AG. dr.boyd@qub.ac.uk
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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