Triazole antifungals. III. Stereocontrolled synthesis of an optically active triazolylmethyloxirane precursor to antifungal oxazolidine derivatives

DOI: 10.1248/cpb.39.2241

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2241 - 2246 (1991)

Update date:2022-08-04

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Authors:

Konosu Konosu

Miyaoka Miyaoka

Tajima Tajima

Oida Oida

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Article abstract of DOI:10.1248/cpb.39.2241

Stereocontrolled synthesis of an optically active triazolylmethyloxirane 2, an important intermediate for the preparation of antifungal oxazolidine compounds 1, was achieved by two methods using L-lactic acid as a starting material. The key intermediate ketone 6 used in the procedures also served for the synthesis of the enantiomer of 2 and the corresponding diastereomeric epoxide.

Full text of DOI:10.1248/cpb.39.2241

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Product name:1-Propanone, 1-(2,4-difluorophenyl)-2-[(methylsulfonyl)oxy]-, (S)-

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