Issue 2, 1986

Azo anions in synthesis: α-amino carbanion equivalents from t-butyldiphenyl-methylhydrazones

Abstract

α-Amino carbanion equivalents ([double bond splayed left][C with combining macron]NH2) and α-hydrazino anion equivalents ([double bond splayed left][C with combining macron]NHNH2) are readily accessible from the C-alkylation products of t-butyldiphenylmethylhydrazones; these azoalkanes can be efficiently transformed into amines, hydrazines, and also alkanes under mild reaction conditions.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 176-178

Azo anions in synthesis: α-amino carbanion equivalents from t-butyldiphenyl-methylhydrazones

J. E. Baldwin, R. M. Adlington and I. M. Newington, J. Chem. Soc., Chem. Commun., 1986, 176 DOI: 10.1039/C39860000176

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