An economical synthesis of Lewis X, sialyl lewis X and their α-galactosyl analogues

Article abstract of DOI:10.1080/07328309708005732

Economical syntheses of the Lewis X trisaccharide 8 and sialyl Lewis X tetrasaccharide 18 epitopes and the syntheses of the α-galactosyl epimers 9 and 20 of these structures are described. Thioglycosides 2, 5, 11 and 15 were used as glycosyl donors to con

Full text of DOI:10.1080/07328309708005732

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Journal of Carbohydrate Chemistry
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An Economical Synthesis of Lewis X,
Sialyl Lewis X and Their α-Galactosyl
Analogues
Gyula Dekany a , Karen Wright a & Istvan Toth a
a The School of Pharmacy, University of London , 29–39 Brunswick
Square, London, WC1N 1AX, UK
Published online: 23 Aug 2006.
To cite this article: Gyula Dekany , Karen Wright & Istvan Toth (1997) An Economical Synthesis of
Lewis X, Sialyl Lewis X and Their α-Galactosyl Analogues, Journal of Carbohydrate Chemistry, 16:7,
983-999, DOI: 10.1080/07328309708005732
To link to this article: http://dx.doi.org/10.1080/07328309708005732
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