Author:
Bebault Gwendolyn M.,Dutton Guy G. S.,Funnell Norman A.
Abstract
4-O-β-D-Galactopyranosyl-L-rhamnopyranose has been synthesized in 60% yield by condensation of 2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl bromide with methyl 2,3-O-isopropylidene-α-L-rhamnopyranoside using mercuric cyanide in acetonitrile (Helferich reaction). The disaccharide is a syrup but the derived alditol and alditol peracetate are crystalline compounds.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
12 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献