Issue 16, 1971

Synthesis of the nucleoside antibiotic formycin B

Abstract

Curtius rearrangement of the 4-azide of 5-(tri-O-benzyl-β-D-ribofuranosyl)pyrazole-3,4-dicarboxylic acid gave the N-carboxy-anhydride of the 4-amino-3-acid the methyl ester of which, on heating in formamide followed by catalytic hydrogenolysis, gave formycin B.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 986-988

Synthesis of the nucleoside antibiotic formycin B

E. M. Acton, K. J. Ryan, D. W. Henry and L. Goodman, J. Chem. Soc. D, 1971, 986 DOI: 10.1039/C29710000986

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