Enantioselective epoxidation of terminal alkenes to (R)- and (S)-epoxides by engineered cytochromes P450 BM-3. (Q33225680)

24 July 2017

title

Enantioselective epoxidation of terminal alkenes to (R)- and (S)-epoxides by engineered cytochromes P450 BM-3. (English)

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24 July 2017

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4

Frances H Arnold

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24 July 2017

Takafumi Kubo

1

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24 July 2017

Matthew W Peters

series ordinal

2

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24 July 2017

Peter Meinhold

series ordinal

3

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24 July 2017

language of work or name

Englisch

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publication date

1 January 2006

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Chemistry—A European Journal

24 July 2017

published in

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24 July 2017

volume

12

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24 July 2017

issue

4

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24 July 2017

page(s)

1216-1220

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A general method of in vitro preparation and specific mutagenesis of DNA fragments: study of protein and DNA interactions

24 July 2017

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An active site substitution, F87V, converts cytochrome P450 BM-3 into a regio- and stereoselective (14S,15R)-arachidonic acid epoxygenase

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High Turnover Numbers for the Catalytic Selective Epoxidation of Alkenes with 1 atm of Molecular Oxygen We acknowledge T. Hayashi (The University of Tokyo), M. Wada (Nippon Shokubai Co., Ltd.), and Y. Sumita (Nippon Shokubai Co., Ltd.) for their hel

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Regio- and enantioselective alkane hydroxylation with engineered cytochromes P450 BM-3.

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Stereoselective hydroxylation of an achiral cyclopentanecarboxylic acid derivative using engineered P450s BM-3.

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11 October 2022

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Identifiers

DOI

10.1002/CHEM.200500584

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24 July 2017

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