Organocatalytic Aerobic Oxidative Monodealkylation of tert-Amines to sec-Amines

13 December 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

The highly efficient monodealkylation of tertiary amines was achieved using hydroxylamine and NOx catalysts under mildly aerobic conditions. This approach demonstrates high functional group tolerance and a broad substrate scope, including amino acids and alkaloids with complex structures. Mechanistic studies have suggested that the reaction proceeds via aminium radical cations via the one-electron oxidation of tertiary amines.

Keywords

amine
oxidative transformation
molecular oxygen
nitroxyl radical
single electron transfer

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