78890-69-4

Upstream product

• 91887-50-2 <1-(2)H>-2,3,4,6-tetra-O-benzyl-α-D-glucopyranose 
• 13096-62-3 (3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-one 
• 78890-54-7 1-O-butanoyl-2,3,4,6-tetra-O-benzyl-α-D-glucopyranose 
• 78890-57-0 Cyclohexanecarboxylic acid (2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl ester 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 78890-59-2 Methoxy-acetic acid (2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl ester 
• 91887-51-3 <1-(2)H>-2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl chloride 

Relevant academic research and scientific papers

Mono-, Di-, and Tri-C-Deuteration of 1,5-Anhydro-D-glucitol

Deuterium was effectively introduced into the title sugar (1a) at C-1, C-3, C-5, and C-6 to afford 1,5-anhydro-D-,-,-, and -glucitols respectively as primary targets for a basic study of the unknown metabolism of 1a, which had

A SIMPLE SYNTHESIS OF (1R and 1S)--1,5-ANHYDRO-D-GLUCITOL AND -1,5-ANHYDRO-D-GLUCITOL

As a basic study of metabolism of 1,5-anhydro-D-glucitol, which has recently been identified in both human cerebrospinal fluid and plasma, the title compounds were conveniently synthesized as preliminary targets not only for multideuteration but for triti