A Broadly Applicable Method for the Efficient Synthesis of α-O-Linked Glycopeptides and Clustered Sialic Acid Residues
Author:
Affiliation:
1. Contribution from the Laboratory for Bioorganic Chemistry, Sloan-Kettering Institute for Cancer Research, 1275 York Avenue, New York, New York 10021, and Department of Chemistry, Columbia University, New York, New York 10027
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja9833265
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1. Glycoconjugates facing the outside world
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3. Immunization of Mice with a Fully Synthetic Globo H Antigen Results in Antibodies against Human Cancer Cells: A Combined Chemical—Immunological Approach to the Fashioning of an Anticancer Vaccine
4. Convergent total synthesis of a tumour-associated mucin motif
5. Efficient syntheses of core 1, core 2, and core 3 and core 4 building blocks for SPS of mucin O-glycopeptides based on the N-Dts-method
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