Issue 16, 1984

N,N-bis(trimethylsilyl)methoxymethylamine as a convenient synthetic equivalent for +CH2NH2: N,N-bis(trimethylsilyl)aminomethylation of silyl sulphides and phosphites

Abstract

N-Silyl-protected primary aminomethyl sulphides and aminomethylphosphonates can be synthesised by the Lewis acid-catalysed reactions of silyl sulphides and silyl phosphites with N,N-bis(trimethylsilyl)methoxymethylamine.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 1055-1056

N,N-bis(trimethylsilyl)methoxymethylamine as a convenient synthetic equivalent for +CH2NH2: N,N-bis(trimethylsilyl)aminomethylation of silyl sulphides and phosphites

T. Morimoto, M. Aono and M. Sekiya, J. Chem. Soc., Chem. Commun., 1984, 1055 DOI: 10.1039/C39840001055

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