NIPPON KAGAKU KAISHI
Online ISSN : 2185-0925
Print ISSN : 0369-4577
Synthetic Studies of 5, 6-Dimethy1-1-(α-D-ribofuranosyl)benzimidazolet
Hideo TSUTSUMIKei OKAZAKIMichiko ASAIKiyotaka ITOHFu-Hua KUANYoshiharu ISHIDO
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1982 Volume 1982 Issue 10 Pages 1682-1691

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Abstract

Two procedures for the synthesis of the title compound, i. e., the coupling reaction of 5, 6dimethylbenzimidazolew ith 2, 3, 5 -tri-O-benzyl-β-D-ribofuranosyblr omide, which was prepared from methyl 2, 3, 5 -tri-O-benzyl-α-o r -β-D-riboluranosideb y treatment with excess acetyl bromide in the presence of a catalytic amount of methanol, and the reaction of 5, 6dimethylbenzimidazolew ith N, N '-diisopropy1-O-(23, - O-isopropylidene-5-O-trityl-D-ribofuranosyl)isourea, which was prepared from diisopropylcarbodiimidaen d the correspongng 1 -OH sugar derivative with the catalytic amount of copper( I) chloride, are described in addition to some basic aspects of the above chemistry. t Partial Protection of Carbohydrate Derivatives. X.

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