Litcius/Paper detail

Nickel-Catalyzed Rearranged Alkenylation of 2-Arylaziridines with Aryl Alkenes to Access Allylamines

Xiangkai Kong, Ming-Bai Gou, Bo Li, Zhen-Qi Luo, Yu Su, Yi Li, Chao Yang, Bin Liu, Qing He, Jiang‐Fei Li, Jiquan Zhang, Jianta Wang, Lei Tang, Rong‐Hua Wang

2025Organic Letters11 citationsDOI

Abstract

The transition-metal-catalyzed ring-opening functionalization of aziridines presents a promising approach for synthesizing structurally complex amines. However, the rearranged functionalization of aziridines poses significant challenges. Herein, we report the first rearranged alkenylation of aziridines with aryl alkenes via Ni-Brønsted acid co-catalysis, leading to the rapid synthesis of a diverse array of allylamines with yields reaching up to 91%. Mechanistic studies suggest that the reaction occurs through the rearrangement of aziridine to generate an imine intermediate. This intermediate is subsequently captured by an alkene under nickel catalysis, ultimately leading to the formation of allylamines.

Topics & Concepts

ChemistryArylCatalysisNickelMedicinal chemistryCombinatorial chemistryOrganic chemistryAlkylSynthesis and Catalytic ReactionsCatalytic C–H Functionalization MethodsSulfur-Based Synthesis Techniques
Nickel-Catalyzed Rearranged Alkenylation of 2-Arylaziridines with Aryl Alkenes to Access Allylamines | Litcius