Stereoselectivity in the enzymic oxidation of racemic alkyl methylcarbinols - A new approach to the L-enantiomers

DOI: 10.1016/S0040-4039(00)78894-0

Source and publish data:

Tetrahedron Letters p. 2009 - 2012 (1991)

Update date:2022-08-29

Topics:

Authors:

Mueller Mueller

Guentherberg

Drechsler

Mauersberger

Kortus Kortus

Oehme Oehme

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Article abstract of DOI:10.1016/S0040-4039(00)78894-0

The R-enantiomers of racemic alkyl methylcarbinols are oxidized specifically by fatty alcohol oxidase (FAOD) from alkane-utilizing yeasts so that the S-enantiomers can be gained in pure state. Fatty alcohol oxidase converts stereospecifically L(-)-enantiomers of alkyl methyl carbinols.

Full text of DOI:10.1016/S0040-4039(00)78894-0

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