Studies on the total synthesis of tallysomycin. Synthesis of the threonylbithiazole moiety containing a structurally unique glycosylcarbinolamide

Marcos L. Sznaidman, Sidney Hecht

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

(equation presented) Tallysomycins are glycopeptide antibiotics that were first isolated from fermentation broths of Streptoalloteichus hindustanus. They are structurally related to the bleomycins but contain an additional talose sugar attached via a unique glycosylcarbinolamide linkage. Herein we report the synthesis of a key tallysomycin intermediate that incorporates the glycosylcarbinolamide moiety unique to the tallysomycins.

Original languageEnglish (US)
Pages (from-to)2811-2814
Number of pages4
JournalOrganic Letters
Volume3
Issue number18
DOIs
StatePublished - Sep 6 2001
Externally publishedYes

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broths
fermentation
antibiotics
sugars
linkages
synthesis
Glycopeptides
Bleomycin
Sugars
Fermentation
Anti-Bacterial Agents
talisomycin

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

Studies on the total synthesis of tallysomycin. Synthesis of the threonylbithiazole moiety containing a structurally unique glycosylcarbinolamide. / Sznaidman, Marcos L.; Hecht, Sidney.

In: Organic Letters, Vol. 3, No. 18, 06.09.2001, p. 2811-2814.

Research output: Contribution to journalArticle

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