Conformational Analysis of Hydroxymethyl Group of D-Mannose Derivatives Using (6S)- and (6R)-(6-2H1)-D-Mannose

Abstract
D-Mannose derivatives stereospecifically deuterated at C-6 were synthesized and the unequivocal 1H NMR assignments of H-6proS and H-6pro R were made. The preferred conformation of the hydroxymethyl groups of these compounds are discussed.

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