Two-step synthesis of the immunogenic bacterial glycolipid BbGL1

Suvarn S. Kulkarni; Jacquelyn Gervay-Hague

doi:10.1021/ol801780c

Two-step synthesis of the immunogenic bacterial glycolipid BbGL1

Suvarn S. Kulkarni, Jacquelyn Gervay-Hague

Chemistry

Research output: Contribution to journal › Article

35 Scopus citations

Abstract

(Chemical Equation Presented) Chemical synthesis of a bacterial glycolipid BbL1 is reported in two steps starting from per-0-TMS D-galactose. The key features are glycosyl iodide mediated β-stereoselective glycosylation in the absence of neighboring group participation and regioseiective acylation.

Original language	English (US)
Pages (from-to)	4739-4742
Number of pages	4
Journal	Organic Letters
Volume	10
Issue number	21
DOIs	https://doi.org/10.1021/ol801780c
State	Published - Dec 1 2008

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ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

Cite this

Kulkarni, S. S., & Gervay-Hague, J. (2008). Two-step synthesis of the immunogenic bacterial glycolipid BbGL1. Organic Letters, 10(21), 4739-4742. https://doi.org/10.1021/ol801780c

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Access to Document

10.1021/ol801780c