Conformationally Switchable Glycosyl Donors
Author:
Affiliation:
1. Department of Chemistry, University of Copenhagen, Universitetsparken 5, DK-2100 Copenhagen, Denmark
Funder
Villum Fonden
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b00830
Reference39 articles.
1. Glycosyl donors in “unusual” conformations – influence on reactivity and selectivity
2. Structure–Reactivity Relationships of Conformationally Armed Disaccharide Donors and Their Use in the Synthesis of a Hexasaccharide Related to the Capsular Polysaccharide from Streptococcus pneumoniae Type 37
3. 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
4. A Study on the Conformation−Anomeric Effect−Stereoselectivity Relationship in Anomeric Radical Reactions, Using Conformationally Restricted Glucose Derivatives as Substrates
5. Highly β-Selective O-Glucosidation Due to the Restricted Twist-Boat Conformation
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