Conformational analyses of α and β (1–6) mannodisaccharides by deuterium substitution effect on relaxation rate and NOE
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Synthesis of (6R)- and (6S)-D-glucose-6-2H through stereospecific photo-bromination of 1,6-anhydro-.BETA.-D-glucopyranose derivative.
2. Syntheses of sugars with a chirally deuterated hydroxymethyl group. Part II. The synthesis of D-(6R)- and (6S)-(6-2H1)-galactose.
3. Chiral Deuteration at C-6 of 1,6-Anhydrohexose Derivatives
4. 1H-NMR studies of (6r)- and (6s)-deuterated d-hexoses: assignment of the preferred rotamers about C5C6 bond of D-glucose and D-galactose derivatives in solutions
5. 1H-NMR Studies on (6R)- and (6S)-deuterated (1–6)-linked disaccharides: assignment of the preferred rotamers about C5–C6 bond of (1–6)-disaccharides in solution
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