Enantiospecific synthesis of optically pure (3s)-hydroxy esters by the stereocontrolled yeast reduction of α-sulfenyl-β-ketoesters |
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| Authors: | Tamotsu Fujisawa Toshiyuki Itoh Toshio Sato |
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| Affiliation: | Chemistry Department of Resources, Mie University, Tsu, Mie 514, Japan |
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| Abstract: | Stereocontrol in Baker's yeast reduction of β-ketoesters was successfully achieved by introducing the sulfenyl group at α-position of the esters to afford optically pure (S)-β-hydroxy esters. |
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