Synthesis of Lewis A and Lewis X pentasaccharides based on N-trichloroethoxycarbonyl protection

Article abstract of DOI:10.1080/07328309808002349

Thexyldimethylsilyl 4,6-O-benzylidene-2-deoxy-2-trichloroethoxycarbonylamino-β-D- glucopyranoside (4), having the 3-hydroxy group unprotected, is a versatile starting material for the synthesis of glucosamine containing oligosaccharides. Thus, reaction wi

Full text of DOI:10.1080/07328309808002349

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Journal of Carbohydrate Chemistry
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Synthesis of Lewis a and Lewis
X Pentasaccharides Based on N-
Trichloroethoxycarbonyl Protection
Leonardo Manzoni a , Luigi Lay a & Richard R. Schmidt a
a Fakultät Chemie , Universität Konstanz , Fach M 725 D-78457,
Konstanz, Germany
Published online: 22 Aug 2006.
To cite this article: Leonardo Manzoni , Luigi Lay & Richard R. Schmidt (1998) Synthesis of Lewis
a and Lewis X Pentasaccharides Based on N-Trichloroethoxycarbonyl Protection , Journal of
Carbohydrate Chemistry, 17:4-5, 739-758
To link to this article: http://dx.doi.org/10.1080/07328309808002349
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