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

Kenichi Takao, Yasuyuki Aiba, Hisanaka Ito, Susumu Kobayashi

研究成果: Article

4 引用 (Scopus)

抄録

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

元の言語English
ページ(範囲)931-932
ページ数2
ジャーナルChemistry Letters
発行部数11
出版物ステータスPublished - 1996
外部発表Yes

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

ASJC Scopus subject areas

  • Chemistry(all)

これを引用

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

:: Chemistry Letters, 番号 11, 1996, p. 931-932.

研究成果: Article

Takao, Kenichi ; Aiba, Yasuyuki ; Ito, Hisanaka ; Kobayashi, Susumu. / Stereoselective route to the highly oxidated sidechain moiety of terpentecin and related antibiotics. :: Chemistry Letters. 1996 ; 番号 11. pp. 931-932.
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