Influence of substitution at the 5α-Position on the side chain conformation of glucopyranosides
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference40 articles.
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2. Probing the influence of a 4,6-O-acetal on the reactivity of galactopyranosyl donors: verification of the disarming influence of the trans-gauche conformation of C5-C6 bonds;Moumé-Pymbock;J. Am. Chem. Soc.,2013
3. Influence of side chain conformation and configuration on glycosyl donor reactivity and selectivity as illustrated by sialic acid donors epimeric at the 7-position;Kancharla;J. Am. Chem. Soc.,2013
4. Stereoselective synthesis of 5-Epi-α-Sialosides related to the pseudaminic acid glycosides. Reassessment of the stereoselectivity of the 5-Azido-5-deacetamidosialyl thioglycosides and use of triflate as nucleophile in the Zbiral deamination of sialic acids;Dhakal;J. Org. Chem.,2016
5. Stereoselective synthesis of the equatorial glycosides of legionaminic acid;Popik;J. Org. Chem.,2017
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