Catalytic Enantioselective Access to N(III)-Stereogenic Aziridines via Chiral Brønsted Acid-Catalyzed N–Cl Bond Formation

Abstract

The asymmetric construction of nitrogen-centered stereogenicity remains one of the longstanding challenges in asymmetric catalysis. Herein, we report an enantioselective synthesis of N-stereogenic aziridines through a chiral phosphoric acid-catalyzed asymmetric N-chlorination, enabling the efficient construction of chiral N(III)-stereogenic aziridines under mild conditions.

Supplementary files

Article information

Article type
Communication
Submitted
23 Apr 2026
Accepted
10 Jun 2026
First published
11 Jun 2026

Chem. Commun., 2026, Accepted Manuscript

Catalytic Enantioselective Access to N(III)-Stereogenic Aziridines via Chiral Brønsted Acid-Catalyzed N–Cl Bond Formation

Y. Zheng, M. Liao, G. Hao, L. Jin, B. C. Jayawardana, B. Marambe, Q. Xiong and X. Wu, Chem. Commun., 2026, Accepted Manuscript , DOI: 10.1039/D6CC02512A

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