JOURNAL ARTICLE

Synthesis of 2-amino-2-deoxy-D-talose and 2-amino-2-deoxy-D-galactose

Malcolm B. PerryAnn Webb

Year: 1968 Journal:   Canadian Journal of Chemistry Vol: 46 (15)Pages: 2481-2484   Publisher: NRC Research Press

Abstract

Treatment of D-lyxose with nitromethane in the presence of sodium methoxide gave 1-deoxy-1-nitro-D-galactitol which, after conversion to 2,3,4,5,6-penta-O-acetyl-1-deoxy-1-nitro-D-galactitol, reacted with saturated methanolic ammonia solution to yield 2-acetamido-1,2-dideoxy-1-nitro-D-talitol and 2-acetamido-1,2-dideoxy-1-nitro-D-galactitol. 2-Acetamido-1,2-dideoxy-1-nitro-D-talitol and 2-acetamido-1,2-dideoxy-1-nitro-D-galactitol were converted by a modified Nef reaction to 2-acetamido-2-deoxy-D-talose and 2-acetamido-2-deoxy-D-galactose which on hydrolysis with hydrochloric acid afforded 2-amino-2-deoxy-D-talose hydrochloride and 2-amino-2-deoxy-D-galactose hydrochloride. The properties and derivatives of the aminoglycoses are described.

Keywords:
Chemistry Galactitol Nitromethane Hydrochloride Nitro Sodium methoxide Hydrolysis Yield (engineering) Stereochemistry Galactose Medicinal chemistry Organic chemistry Methanol

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Citation History

Topics

Diet, Metabolism, and Disease
Health Sciences →  Medicine →  Endocrinology, Diabetes and Metabolism
Amino Acid Enzymes and Metabolism
Life Sciences →  Biochemistry, Genetics and Molecular Biology →  Biochemistry
Carbohydrate Chemistry and Synthesis
Physical Sciences →  Chemistry →  Organic Chemistry
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