Synthesis of 3,6-O-(o-Xylylene)glucopyranosyl Fluoride, an Axial-Rich Glycosyl Donor of β-Glycosylation
Author:
Affiliation:
1. School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda 669-1337, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo401395h
Reference49 articles.
1. Methodology Development and Physical Organic Chemistry: A Powerful Combination for the Advancement of Glycochemistry
2. On the Reactivity and Selectivity of Galacturonic Acid Lactones
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4. Can the stereochemical outcome of glycosylation reactions be controlled by the conformational preferences of the glycosyl donor?
5. The two-conformer hypothesis: 2,3,4,6-tetra-O-methyl-mannopyranosyl and -glucopyranosyl oxacarbenium ions
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