Issue 18, 1971

The nitrous acid deamination of methyl 4-amino-4-deoxy-α-D-galactopyranoside and 3-amino-3-deoxy-β-D-allopyranoside

Abstract

Rearrangements are important reaction pathways in the deamination of the pyranoside amines (II) and (IV).

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 1123-1124

The nitrous acid deamination of methyl 4-amino-4-deoxy-α-D-galactopyranoside and 3-amino-3-deoxy-β-D-allopyranoside

N. M. K. N. Y. Kin and J. M. Williams, J. Chem. Soc. D, 1971, 1123 DOI: 10.1039/C29710001123

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