The new and efficient synthesis of a heptose moiety of spicamycin

Tamotsu Suzuki; Noritaka Chida

doi:10.1246/cl.2003.190

The new and efficient synthesis of a heptose moiety of spicamycin

Tamotsu Suzuki, Noritaka Chida

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

11 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 language	English
Pages (from-to)	190-191
Number of pages	2
Journal	Chemistry Letters
Volume	32
Issue number	2
DOIs	https://doi.org/10.1246/cl.2003.190
Publication status	Published - 2003 Feb 5
Externally published	Yes

ASJC Scopus subject areas

Chemistry(all)

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1246/cl.2003.190

Cite this

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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.",

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AU - Chida, Noritaka

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The new and efficient synthesis of a heptose moiety of spicamycin

Abstract

ASJC Scopus subject areas

UN SDGs

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