Highly α- and β-Selective Radical C-Glycosylation Reactions Using a Controlling Anomeric Effect Based on the Conformational Restriction Strategy. A Study on the Conformation−Anomeric Effect− Stereoselectivity Relationship in Anomeric Radical Reactions
Author:
Affiliation:
1. Contribution from the Graduate School of Pharmaceutical Sciences, Hokkaido University, Kita-12, Nishi-6, Kita-ku, Sapporo 060-0812, Japan
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja011321t
Reference53 articles.
1. The structure and configuration of pseudomonic acid C
2. Synthesis of diazomethyl β-d-galactopyranosyl and β-d-glucopyranosyl ketones. Potential affinity-labeling reagents for carbohydrate-binding proteins
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