Efficient, one-pot syntheses of biologically active α-linked glycolipids

Wenjun Du; Suvarn S. Kulkarni; Jacquelyn Gervay-Hague

doi:10.1039/b702551c

Efficient, one-pot syntheses of biologically active α-linked glycolipids

Wenjun Du, Suvarn S. Kulkarni, Jacquelyn Gervay-Hague

https://www.cmich.edu/academics/colleges/college-science-engineering/departments-schools/chemistry-and-biochemistry

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

84 Scopus citations

Abstract

Per-O-silylated galactosyl iodides undergo α-glycosidation with fully functionalized glycolipids producing biologically relevant conjugates.

Original language	English
Pages (from-to)	2336-2338
Number of pages	3
Journal	Chemical Communications
Issue number	23
DOIs	https://doi.org/10.1039/b702551c
State	Published - 2007

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title = "Efficient, one-pot syntheses of biologically active α-linked glycolipids",

abstract = "Per-O-silylated galactosyl iodides undergo α-glycosidation with fully functionalized glycolipids producing biologically relevant conjugates.",

author = "Wenjun Du and Kulkarni, {Suvarn S.} and Jacquelyn Gervay-Hague",

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AU - Du, Wenjun

AU - Kulkarni, Suvarn S.

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N2 - Per-O-silylated galactosyl iodides undergo α-glycosidation with fully functionalized glycolipids producing biologically relevant conjugates.

AB - Per-O-silylated galactosyl iodides undergo α-glycosidation with fully functionalized glycolipids producing biologically relevant conjugates.

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SP - 2336

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JO - Chemical Communications

JF - Chemical Communications

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Efficient, one-pot syntheses of biologically active α-linked glycolipids

Abstract

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