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

Kenichi Takao, Yasuyuki Aiba, Hisanaka Ito, Susumu Kobayashi

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

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

Original languageEnglish
Pages (from-to)931-932
Number of pages2
JournalChemistry Letters
Issue number11
Publication statusPublished - 1996
Externally publishedYes

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Anti-Bacterial Agents
1,2-5,6-di-O-isopropylidene-D-glucofuranose
terpentecin

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Stereoselective route to the highly oxidated sidechain moiety of terpentecin and related antibiotics. / Takao, Kenichi; Aiba, Yasuyuki; Ito, Hisanaka; Kobayashi, Susumu.

In: Chemistry Letters, No. 11, 1996, p. 931-932.

Research output: Contribution to journalArticle

Takao, Kenichi ; Aiba, Yasuyuki ; Ito, Hisanaka ; Kobayashi, Susumu. / Stereoselective route to the highly oxidated sidechain moiety of terpentecin and related antibiotics. In: Chemistry Letters. 1996 ; No. 11. pp. 931-932.
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