(Q59488903)

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Dibutylstannylene acetals: Useful intermediates for the regioselective sulfation of glycosides

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Dibutylstannylene acetals: Useful intermediates for the regioselective sulfation of glycosides (English)

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author name string

Bénédicte Guilbert

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1

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Nicola J. Davis

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2

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Melanie Pearce

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3

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Robin T. Aplin

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4

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Sabine L. Flitsch

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5

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publication date

November 1994

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published in

Tetrahedron: Asymmetry

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volume

5

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issue

11

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page(s)

2163-2178

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cites work

Novel sulfated ligands for the cell adhesion molecule E-selectin revealed by the neoglycolipid technology among O-linked oligosaccharides on an ovarian cystadenoma glycoprotein

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Simple procedures for the rapid cleavage of ester lipids and for the large-scale isolation from brain of cerebroside sulfate

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Regioselective sulfation of disaccharides using dibutylstannylene acetals

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The regioselective tert-butyldimenthylsilylation of the 6′-hydroxyl group of lactose derivatives via their dibutylstannylene acetals

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Sulfation of Alcohols with Arylsulfuryl Chlorides. I. : Monosulfation of Monosaccharides

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Studies on the three-dimensional behaviour of the selectin ligands Lewis(a) and sulphated Lewis(a) using NMR spectroscopy and molecular dynamics simulations

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https://api.crossref.org/works/10.1016%2FS0957-4166%2800%2986292-8

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6'-sulfated sialyl Lewis x is a major capping group of GlyCAM-1.

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10.1016/S0957-4166(00)86292-8

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(Q59488903)

Dibutylstannylene acetals: Useful intermediates for the regioselective sulfation of glycosides

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