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

5 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)

Access to Document

10.1246/cl.1996.931

Cite this

@article{3a186b92141c474583ae6ea2f455d4f4,

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",

month = jan,

day = "1",

doi = "10.1246/cl.1996.931",

language = "English",

pages = "931--932",

journal = "Chemistry Letters",

issn = "0366-7022",

publisher = "Chemical Society of Japan",

number = "11",

}

TY - JOUR

T1 - Stereoselective route to the highly oxidated sidechain moiety of terpentecin and related antibiotics

AU - Takao, Ken Ichi

AU - Aiba, Yasuyuki

AU - Ito, Hisanaka

AU - Kobayashi, Susumu

PY - 1996/1/1

Y1 - 1996/1/1

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

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

UR - http://www.scopus.com/inward/record.url?scp=0030351673&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0030351673&partnerID=8YFLogxK

U2 - 10.1246/cl.1996.931

DO - 10.1246/cl.1996.931

M3 - Article

AN - SCOPUS:0030351673

SP - 931

EP - 932

JO - Chemistry Letters

JF - Chemistry Letters

SN - 0366-7022

IS - 11

ER -

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

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this