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Highly diastereo- and enantio-selective epoxidation of secondary allylic alcohols catalyzed by styrene monooxygenase

Enantiomerically enriched glycidol derivatives with contiguous stereogenic centers were obtained in a highly diastereo- and enantio-selective epoxidation catalyzed with the styrene monooxygenase StyAB2.

Journal Title: Chemical Communications 2011, Vol.47(9), pp.2610-2612
Main Author: Lin, Hui
Other Authors: Liu, Yan , Wu, Zhong-liu
Format: Electronic Article Electronic Article
Language:
Subjects:
ID: ISSN: 1359-7345 ; E-ISSN: 1364-548X ; DOI: 10.1039/c0cc04360e
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recordid: rscc0cc04360e
title: Highly diastereo- and enantio-selective epoxidation of secondary allylic alcohols catalyzed by styrene monooxygenase
format: Article
creator:
  • Lin, Hui
  • Liu, Yan
  • Wu, Zhong-liu
subjects:
  • Oxygenases -- Metabolism
  • Propanols -- Chemistry
ispartof: Chemical Communications, 2011, Vol.47(9), pp.2610-2612
description: Enantiomerically enriched glycidol derivatives with contiguous stereogenic centers were obtained in a highly diastereo- and enantio-selective epoxidation catalyzed with the styrene monooxygenase StyAB2.
language:
source:
identifier: ISSN: 1359-7345 ; E-ISSN: 1364-548X ; DOI: 10.1039/c0cc04360e
fulltext: fulltext
issn:
  • 1359-7345
  • 1364-548X
  • 1364548X
  • 13597345
url: Link


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descriptionEnantiomerically enriched glycidol derivatives with contiguous stereogenic centers were obtained in a highly diastereo- and enantio-selective epoxidation catalyzed with the styrene monooxygenase StyAB2.
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abstractEnantiomerically enriched glycidol derivatives with contiguous stereogenic centers were obtained in a highly diastereo- and enantio-selective epoxidation catalyzed with the styrene monooxygenase StyAB2.
doi10.1039/c0cc04360e
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date2011-02-14