Stereoselective route to the highly oxidated sidechain moiety of terpentecin and related antibiotics

DOI: 10.1246/cl.1996.931

Source and publish data:

Chemistry Letters p. 931 - 932 (1996)

Update date:2022-07-30

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Authors:

Takao, Ken-Ichi

Aiba, Yasuyuki

Ito, Hisanaka

Kobayashi, Susumu

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Article abstract of DOI:10.1246/cl.1996.931

Highly oxidated sidechain moiety of antitumor terpentecin and related antibiotics is prepared in a stereoselective manner from diacetone glucose through furanoside intermediates.

Full text of DOI:10.1246/cl.1996.931

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