Halogenation-enabled intramolecular deaminative cyclization

Abstract

Carbon–nitrogen (C–N) bonds are traditionally inert toward nucleophilic attack. Herein, we present a halogenation-induced C–N bond activation strategy that enables the intramolecular substitution of secondary and tertiary amino groups by hydroxyl, amino, carboxyl, or thiol groups, providing an efficient method for amine transformation.

Graphical abstract: Halogenation-enabled intramolecular deaminative cyclization

Supplementary files

Article information

Article type
Communication
Submitted
31 Mar 2025
Accepted
13 May 2025
First published
19 May 2025

Org. Biomol. Chem., 2025, Advance Article

Halogenation-enabled intramolecular deaminative cyclization

W. Wang and G. He, Org. Biomol. Chem., 2025, Advance Article , DOI: 10.1039/D5OB00535C

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