Borinic Acid Catalyzed Stereo- and Regioselective Couplings of Glycosyl Methanesulfonates
Author:
Affiliation:
1. Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario M5S 3H6, Canada
Funder
Canada Foundation for Innovation
Canada Research Chairs
Natural Sciences and Engineering Research Council of Canada
Ontario Ministry of Research and Innovation
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.6b06943
Reference81 articles.
1. Are Glycosyl Triflates Intermediates in the Sulfoxide Glycosylation Method? A Chemical and 1H, 13C, and 19F NMR Spectroscopic Investigation
2. A General Strategy for Stereoselective Glycosylations
3. Highly β-Selective O-Glucosidation Due to the Restricted Twist-Boat Conformation
4. Acceleration of Acetal Hydrolysis by Remote Alkoxy Groups: Evidence for Electrostatic Effects on the Formation of Oxocarbenium Ions
5. 6-O-Picolinyl and 6-O-Picoloyl Building Blocks As Glycosyl Donors with Switchable Stereoselectivity
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