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

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概要

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• Deuterium was effectively introduced into the title sugar (<B>1a</B>) at C-1, C-3, C-5, and C-6 to afford 1,5-anhydro-D-[1-<SUP>2</SUP>H<SUB>1</SUB>], -[3-<SUP>2</SUP>H], -[5-<SUP>2</SUP>H], -[1-<SUP>2</SUP>H<SUB>2</SUB>], -[6-<SUP>2</SUP>H<SUB>2</SUB>], and -[5,6-<SUP>2</SUP>H<SUB>3</SUB>]glucitols respectively as primary targets for a basic study of the unknown metabolism of <B>1a</B>, which had been suggested to be a candidate of metabolic indexes for insulin-dependent diabetes mellitus.

• 公益社団法人 日本化学会の論文

著者

• Funabashi Masuo

  Chemistry Department, College of Arts and Sciences, Chiba University

• Hasegawa Toshimori

  Chemistry Department, College of Arts and Sciences, Chiba University

関連論文

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

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