Synthesis of a Neolactotetraose Glycoside Suitable for Enzymatic Elaboration to the Sialyl Lewis X Stage
Author:
Affiliation:
1. a Department of Chemistry, Faculty of Science , Alexandria University , Ebrahemia P.O. Box 426, Alexandria, 21321, EGYPT
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/07328309808002327
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1. A Convenient Synthesis of Partially Benzylated Derivative of β-DGlcpNAc-( 1→3)-β-D-Galp-(1→4)-β-D-Glcp-1-OBn as a Versatile Building Block for Sialyl Lewis X Antigens;Letters in Organic Chemistry;2015-06-04
2. ChemInform Abstract: Synthesis of a Neolactotetraose Glycoside Suitable for Enzymatic Elaboration to the Sialyl Lewis X Stage.;ChemInform;2010-06-20
3. Syntheses of a series of lacto-N-neotetraose clusters using a carbosilane dendrimer scaffold;Carbohydrate Research;2006-03
4. Study of glycosylation with N-trichloroacetyl-d-glucosamine derivatives in the syntheses of the spacer-armed pentasaccharides sialyl lacto-N-neotetraose and sialyl lacto-N-tetraose, their fragments, and analogues;Carbohydrate Research;2001-11
5. Synthesis of Sialyl-α-(2→3)-Neolactotetraose Derivatives Containing Different Sialic Acids: Molecular Probes for Elucidation of Substrate Specificity of Human α1,3-Fucosyltransferases;Journal of Carbohydrate Chemistry;2000-01
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