Stereoselective C-Glycosylation from Glycal Scaffolds
Author:
Affiliation:
1. Nanyang Technological University; Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences; SPMS-CBC-02-01 New York 21 Nanyang Link, 637371 Singapore
Publisher
Wiley-VCH Verlag GmbH & Co. KGaA
Reference72 articles.
1. Glycobiology: Toward Understanding the Function of Sugars
2. Rational Design of an Aryl-C-Glycoside Catalyst from a Natural Product O-Glycosyltransferase
3. Fluorescence Anisotropy Assays Reveal Affinities of C- and O-Glycosides for Concanavalin A1
4. Bioactive C-Glycosides from Bacterial Secondary Metabolism
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1. Stereoselective Synthesis of Glycosides via Tsuji–Trost Type Glycosylation Using 3,4‐Carbonate Galactals;The Chemical Record;2024-08-21
2. Selective Reduction Leading to 3,5-cis-3-Aminosugars: Synthesis and Stereoselective Glycosylation;The Journal of Organic Chemistry;2022-12-14
3. From Glycals to Nitrogen Heterocycles and Carbocycles via “Cleavage‐Intramolecular Recombination Strategy”;The Chemical Record;2021-09-02
4. Light-Mediated Cross-Coupling of Anomeric Trifluoroborates;Organic Letters;2021-05-24
5. 1,2-trans-Stereoselective Synthesis of C-Glycosides of 2-Deoxy-2-amino-sugars Involving Glycosyl Radicals;Organic Letters;2021-03-18
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