Eukaryotic glycosylation: whim of nature or multipurpose tool?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Cellular and Molecular Neuroscience,Pharmacology,Molecular Biology,Molecular Medicine
Link
http://link.springer.com/content/pdf/10.1007/s000180050298.pdf
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1. Dynamic Kinetic Stereoselective Glycosylation via RhII and Chiral Phosphoric Acid‐Cocatalyzed Carbenoid Insertion to the Anomeric OH Bond for the Synthesis of Glycoconjugates;Angewandte Chemie International Edition;2023-08-21
2. Dynamic Kinetic Stereoselective Glycosylation via RhII and Chiral Phosphoric Acid‐Cocatalyzed Carbenoid Insertion to the Anomeric OH Bond for the Synthesis of Glycoconjugates;Angewandte Chemie;2023-08-21
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4. Targeting osteoarthritis-associated galectins and an induced effector class by a ditopic bifunctional reagent: Impact of its glycan part on binding measured in the tissue context;Bioorganic & Medicinal Chemistry;2022-12
5. A Sweet Warning: Mucin-Type O-Glycans in Cancer;Cells;2022-11-18
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