91887-50-2Relevant academic research and scientific papers
Mono-, Di-, and Tri-C-Deuteration of 1,5-Anhydro-D-glucitol
Funabashi, Masuo,Hasegawa, Toshimori
, p. 2528 - 2531 (1991)
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
Funabashi, Masuo,Yoshioka, Shigetake
, p. 677 - 680 (2007/10/02)
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
