Kinetically Controlled α-SelectiveO-Glycosylation of Phenol Derivatives Using 2-Nitroglycals by a Bifunctional Chiral Thiourea Catalyst
Author:
Affiliation:
1. Institute for Chemical Research; Kyoto University, Gokasho, Uji; Kyoto 611-0011 Japan
2. Department of Applied Chemistry; Keio University, Hiyoshi, Kohoku-ku; Yokohama 223-8522 Japan
Funder
Keio Gijuku Academic Development Funds
Publisher
Wiley
Subject
Organic Chemistry
Reference77 articles.
1. Aromatic O-glycosylation
2. New approach to C-aryl glycosides starting from phenol and glycosyl fluoride. Lewis acid-catalyzed rearrangement of O-glycoside to C-glycoside
3. Boron Trifluoride-Catalyzed Rearrangement of 2-Aryloxytetrahydropyrans: A New Entry to C-Arylglycosidation
4. Improvement in O→C-glycoside rearrangement approach to C-aryl glycosides: Use of 1-O-acetyl sugar as stable but efficient glycosyl donor
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