HIGHLY ENANTIO- AND DIASTEREOSELECTIVE REDUCTION OF SULFUR-FUNCTIONALIZED CYCLIC KETONES WITH BAKER'S YEAST

DOI: 10.1016/S0040-4039(00)92638-8

Source and publish data:

Tetrahedron Letters p. 399 - 400 (1991)

Update date:2022-08-02

Topics:

Authors:

Fujisawa, Tamotsu

Yamanaka, Kengo

Mobele, Bingidimi I.

Shimizu, Makoto

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Article abstract of DOI:10.1016/S0040-4039(00)92638-8

Baker's yeast reduction of 2-phenylthiocyclopentanone, 2-phenylthiocyclohexanone, and 2-phenylthio-2-cyclopentenone affords the corresponding (1S,2R)-2-phenylthiocycloalkanols in optically pure form and excellent diastereomeric excess.

Full text of DOI:10.1016/S0040-4039(00)92638-8

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