SYNTHESIS AND ABSOLUTE STEREOCHEMISTRY OF SERRICORNIN

DOI: 10.1016/0040-4020(82)80081-1

Source and publish data:

Tetrahedron p. 3705 - 3712 (1982)

Update date:2022-08-05

Topics:

Authors:

Mori, Kenji

Nomi, Hiroko

Chuman, Tatsuji

Kohno, Masahiro

Kato, Kunio

Noguchi, Masao

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Article abstract of DOI:10.1016/0040-4020(82)80081-1

The absolute stereochemistry of serricornin (4,6-dimethyl-7-hydroxy-3-nonanone) was established as 4S, 6S, 7S by synthesizing both (4S, 6S, 7S)-isomer and its antipode.Only the natural enantiomer was bioactive.by

Full text of DOI:10.1016/0040-4020(82)80081-1

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