Characterization of the low energy conformations and differential reactivities of d-glucose and d-mannose based oxepines
Author:
Affiliation:
1. Department of Chemistry, University of Connecticut, 55 N. Eagleville Road, U3060, Storrs, CT 06269-3060, USA
Abstract
Funder
National Science Foundation
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB01900G
Reference49 articles.
1. Septanose Carbohydrates: Synthesis and Conformational Studies of Methyl α-d-glycero-d-Idoseptanoside and Methyl β-d-glycero-d-Guloseptanoside
2. Carbohydrate-based oxepines: ring expanded glycals for the synthesis of septanose saccharides
3. Synthesis and Conformational Study of Chiral Oxepines: The Baylis−Hillman Reaction and RCM Approach with Sugar Aldehyde
4. An expeditious route to the synthesis of highly functionalized chiral oxepines from monosaccharides
5. 1,5-α-d-Mannoseptanosides, Ring-Size Isomers That Are Impervious to α-Mannosidase-Catalyzed Hydrolysis
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