Issue 17, 1970

A simple synthesis in high yield of 2,3-O-isopropylidene-β-D-ribofuranosylamine, an intermediate in the preparation of N-substituted ribofuranosides

Abstract

2,3-Isopropylidene-β-D-ribofuranosylamine is obtained in high yield by the reaction of D-ribopyranosylamine with acetone, 2,2-dimethoxypropane, and toluene-p-sulphonic acid.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 1114-1114

A simple synthesis in high yield of 2,3-O-isopropylidene-β-D-ribofuranosylamine, an intermediate in the preparation of N-substituted ribofuranosides

N. J. Cusack and G. Shaw, J. Chem. Soc. D, 1970, 1114 DOI: 10.1039/C29700001114

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