Abstract
The mono-, di-, and tri-O-methyl ether derivatives of 2-amino-2-deoxy-D-glucopyranose have been analyzed by gas–liquid chromatography of their fully acetylated 2-acetamido-2-deoxy-D-glucitol derivatives which were prepared from the glycoses by reduction with sodium borohydride followed by acetylation with acetic anhydride. The methyl ethers of 2-amino-2-deoxy-D-glucopyranose were also characterized by degradation with ninhydrin to the corresponding methyl ether derivatives of D-arabinose which were identified by paper chromatography.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
16 articles.
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