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

Ken Ichi Takao; Yasuyuki Aiba; Hisanaka Ito; Susumu Kobayashi

doi:10.1246/cl.1996.931

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

Ken Ichi Takao, Yasuyuki Aiba, Hisanaka Ito, Susumu Kobayashi

Research output: Contribution to journal › Article › peer-review

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 language	English
Pages (from-to)	931-932
Number of pages	2
Journal	Chemistry Letters
Issue number	11
DOIs	https://doi.org/10.1246/cl.1996.931
Publication status	Published - 1996 Jan 1
Externally published	Yes

ASJC Scopus subject areas

Chemistry(all)

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10.1246/cl.1996.931

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title = "Stereoselective route to the highly oxidated sidechain moiety of terpentecin and related antibiotics",

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

author = "Takao, {Ken Ichi} and Yasuyuki Aiba and Hisanaka Ito and Susumu Kobayashi",

year = "1996",

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doi = "10.1246/cl.1996.931",

language = "English",

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AU - Takao, Ken Ichi

AU - Aiba, Yasuyuki

AU - Ito, Hisanaka

AU - Kobayashi, Susumu

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N2 - Highly oxidated sidechain moiety of antitumor terpentecin and related antibiotics is prepared in a stereoselective manner from diacetone glucose through furanoside intermediates.

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DO - 10.1246/cl.1996.931

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JO - Chemistry Letters

JF - Chemistry Letters

SN - 0366-7022

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