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 |
| Publication status | Published - 1996 |
| Externally published | Yes |
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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 journal › Article
}
TY - JOUR
T1 - Stereoselective route to the highly oxidated sidechain moiety of terpentecin and related antibiotics
AU - Takao, Kenichi
AU - Aiba, Yasuyuki
AU - Ito, Hisanaka
AU - Kobayashi, Susumu
PY - 1996
Y1 - 1996
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
M3 - Article
SP - 931
EP - 932
JO - Chemistry Letters
JF - Chemistry Letters
SN - 0366-7022
IS - 11
ER -