A versatile approach to the synthesis of glycans containing mannuronic acid residues
Author:
Affiliation:
1. Department of Chemistry and Biochemistry
2. University of Missouri – St Louis
3. One University Boulevard
4. St Louis
5. USA
Abstract
Reported herein is a highly stereocontrolled synthesis of α or β-glycosides of mannuronic acid from glycosyl donors equipped with the 3-O-benzoyl or 3-O-picoloyl group, respectively.
Funder
Division of Chemistry
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB00188D
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5. Glycosidation Reactions of Silyl Ethers with Conformationally Inverted Donors Derived from Glucuronic Acid: Stereoselective Synthesis of Glycosides and 2-Deoxyglycosides
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