OPTICALLY PURE (S)-3-PHENYLTHIO-1,2-PROPANEDIOL: SYNTHESIS BY THE YEAST REDUCTION AND USE AS A PRECURSOR OF BOTH ENANTIOMERS OF SECONDARY ALCOHOLS

DOI: 10.1016/S0040-4039(00)89133-9

Source and publish data:

Tetrahedron Letters p. 771 - 774 (1985)

Update date:2022-07-31

Topics:

Authors:

Fujisawa, Tamotsu

Itoh, Toshiyuki

Nakai, Mikio

Sato, Toshio

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Article abstract of DOI:10.1016/S0040-4039(00)89133-9

Optically pure (S)-3-phenylthio-1,2-propanediol was obtained by the enantioselective reduction of 1-hydroxy-3-phenylthio-2-propanone with the Baker's yeast, and was found to be a convenient precursor for both enantiomers of secondary alcohols, which was d

Full text of DOI:10.1016/S0040-4039(00)89133-9

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Product name:Oxirane, (3-phenylpropyl)-, (S)-

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