用于氢原子转移反应的N-羟基苯并咪唑催化剂的探索†

Zhi-Xian Wu , Xue-Tao Xu , Yu-Xin Luan
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引用次数: 0

摘要

N-羟基苯并咪唑(NHBIs)已被证明是有效的氢原子吸附剂(HAAs),但自首次报道以来,它们在催化中的进一步应用很少被探索。在此,我们描述了它们在其他氢原子转移反应中的催化性能。具体而言,我们通过级联[3+2]环化-芳构化实现了铜/NHBI共催化合成2-膦基吡咯。NHBI被证明在环化步骤和随后的芳构化中起着至关重要的作用。此外,NHBI催化的亚胺环化和C–H氧化也是可行的。值得注意的是,带有可以识别底物的对接基团的NHBI也首次被研究为双功能HAT催化剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exploration of N-hydroxy benzimidazole catalysts for hydrogen atom transfer reactions†

Exploration of N-hydroxy benzimidazole catalysts for hydrogen atom transfer reactions†

N-Hydroxy benzimidazoles (NHBIs) have proved to be efficient hydrogen atom abstractors (HAAs), but their further application in catalysis has been rarely explored since the first report. Herein, we describe their catalytic performance in other hydrogen atom transfer reactions. Specifically, we realized a copper/NHBI co-catalyzed synthesis of 2-phosphonopyrroles via cascade [3 + 2] annulation–aromatization. And NHBI was demonstrated to play a crucial role in both the annulation step and the subsequent aromatization. Besides, NHBI-catalyzed annulation with an imine and C–H oxidation were also feasible. Notably, NHBIs bearing a docking group that can recognize substrates were also investigated as bifunctional HAT catalysts for the first time.

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