Issue 3, 1984

Base-promoted rearrangement of siloxyammonium salts: a new method of dealkylation of tertiary amines via their N-oxides

Abstract

Siloxyammonium salts prepared from tertiary amine N-oxides and trialkylsilyl trifluoromethanesulphonate undergo rearrangement in the presence of strong bases to give α-siloxyamines, which can be converted into secondary amine derivatives.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 192-193

Base-promoted rearrangement of siloxyammonium salts: a new method of dealkylation of tertiary amines via their N-oxides

R. Okazaki and N. Tokitoh, J. Chem. Soc., Chem. Commun., 1984, 192 DOI: 10.1039/C39840000192

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