β‐Selective Glycosylation by Using O ‐Aryl‐Protected Glycosyl Donors
Author:
Affiliation:
1. Department of ChemistryGraduate School of ScienceOsaka University Machikaneyama 1-1 Toyonaka Osaka Prefecture 560-0043 Japan
2. Peptide Institute, Inc. Saito-Asagi 7-2-9 Ibaraki Osaka Prefecture 567-0085 Japan
Funder
Japan Society for the Promotion of Science
Publisher
Wiley
Subject
General Chemistry,Biochemistry,Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/asia.201900700
Reference34 articles.
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1. Stereoselective AromaticO-Glycosylation of Glycosyl Chloride with Arylboronic Acid under an Air Atmosphere;The Journal of Organic Chemistry;2023-07-24
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3. Single‐Step Glycosylations with 13 C‐Labelled Sulfoxide Donors: A Low‐Temperature NMR Cartography of the Distinguishing Mechanistic Intermediates;Chemistry – A European Journal;2020-11-23
4. Synthesis of Arylated Carbohydrates and Their Application;Trends in Glycoscience and Glycotechnology;2020-09-25
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