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

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

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DOI 10.1039/b702551c

Journal Chem. Commun.
Location p 2336-2338, Issue 23, 2007
Publication Type journal-article

Tags glycolipids, biological activity, materials chemistry, electronic, optical and magnetic materials, chemistry(all), surfaces, coatings and films, metals and alloys, ceramics and composites, catalysis
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Paper Abstract Per- O -silylated galactosyl iodides undergo α-glycosidation with fully functionalized glycolipids producing biologically relevant conjugates.

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09 Dec 2016

Anonymous

(1)

Adjustments needed to increase efficiency of methodology

Reproducibility

Clarity

Versatility

The methodology described in this article is very valuable for scientists working with glycosphingolipids. It provided a one-pot syntheses of alpha-linked glycolipids with the possibility of using substrates with unsaturations in the fatty acid side chains. This was a challenge...

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

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

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Adjustments needed to increase efficiency of methodology

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