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Enantioselective reduction of α,β-unsaturated ketones by Geotrichum candidum, Mortierella isabellina and Rhodotorula rubra yeast
The reduction of 3-methyl-4-phenyl-3-buten-2-one and its phenyl-substituted derivatives by microorganisms was investigated. Growing cells of Mortierella isabellina DSM1414 and Geotrichum candidum LOCK 105 strains reduced α,β-unsaturated ketones to the corresponding secondary alcohols in high enantio...
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Published in: | Tetrahedron: asymmetry 2006-08, Vol.17 (13), p.1958-1962 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The reduction of 3-methyl-4-phenyl-3-buten-2-one and its phenyl-substituted derivatives by microorganisms was investigated. Growing cells of
Mortierella isabellina DSM1414 and
Geotrichum candidum LOCK 105 strains reduced α,β-unsaturated ketones to the corresponding secondary alcohols in high enantiomeric excess (94–99%), whereas the
Rhodotorula rubra M18D3 strain converted the same compounds into optically active ketones as the major products with only trace amounts of the corresponding saturated and unsaturated alcohols. |
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ISSN: | 0957-4166 1362-511X |
DOI: | 10.1016/j.tetasy.2006.06.021 |