Source:http://linkedlifedata.com/resource/pubmed/id/19277363
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2009-3-11
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pubmed:abstractText |
Chiral aryl vicinal diols were obtained in high ee and yield by asymmetric dihydroxylation of aryl olefins with tandem biocatalysts: one contains an enantioselective styrene monooxygenase, and the other contains a regioselective epoxide hydrolase.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1359-7345
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1481-3
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:19277363-Alkenes,
pubmed-meshheading:19277363-Biocatalysis,
pubmed-meshheading:19277363-Epoxide Hydrolases,
pubmed-meshheading:19277363-Escherichia,
pubmed-meshheading:19277363-Hydroxylation,
pubmed-meshheading:19277363-Molecular Structure,
pubmed-meshheading:19277363-Oxygenases,
pubmed-meshheading:19277363-Sphingomonas,
pubmed-meshheading:19277363-Stereoisomerism
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pubmed:year |
2009
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pubmed:articleTitle |
Asymmetric dihydroxylation of aryl olefins by sequential enantioselective epoxidation and regioselective hydrolysis with tandem biocatalysts.
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pubmed:affiliation |
Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore 117576.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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