Issue 19, 1983

Monoalkylation of primary aromatic amines via N-(alkoxymethyl)aryl amines. Evidence for the formation of stable monomeric methyleneamines

Abstract

Monomeric methyleneamines (1), formed from N-(alkoxymethyl)arylamines (3), are stable at –60 °C and may be trapped with organometallic reagents to provide the N-alkylarylamines (7).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 1109-1110

Monoalkylation of primary aromatic amines via N-(alkoxymethyl)aryl amines. Evidence for the formation of stable monomeric methyleneamines

J. Barluenga, A. M. Bayón and G. Asensio, J. Chem. Soc., Chem. Commun., 1983, 1109 DOI: 10.1039/C39830001109

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