The new and efficient synthesis of a heptose moiety of spicamycin

Tamotsu Suzuki, Noritaka Chida

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

The new and efficient synthesis of 7-O-acetyl-4-azido-2,3,6-tri-O-benzyl-4-deoxy-L-glycero-α-L-manno- heptopyranosyl acetate (5), a key intermediate for the synthesis of novel anti-cancer antibiotic, spicamycin (1), starting from D-ribose is described.

Original languageEnglish
Pages (from-to)190-191
Number of pages2
JournalChemistry Letters
Volume32
Issue number2
DOIs
Publication statusPublished - 2003 Feb 5

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Heptoses
Ribose
Acetates
Anti-Bacterial Agents
septacidin

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

The new and efficient synthesis of a heptose moiety of spicamycin. / Suzuki, Tamotsu; Chida, Noritaka.

In: Chemistry Letters, Vol. 32, No. 2, 05.02.2003, p. 190-191.

Research output: Contribution to journalArticle

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