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基于具有高结构可调性的碳中心自由基的鏻叶立德作为氢原子转移催化剂平台

Phosphonium Ylide as Hydrogen Atom Transfer Catalyst Platform Based on Carbon-Centered Radical with High Structural Tunability.

作者信息

Caner Joaquim, Maeda Natsumi, Yokogawa Daisuke, Matsumoto Akira, Maruoka Keiji

机构信息

Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo, Kyoto 606-8501, Japan.

Graduate School of Arts and Sciences, The University of Tokyo, Komaba, Meguro-ku, Tokyo 153-8902, Japan.

出版信息

JACS Au. 2025 Jun 9;5(6):2463-2468. doi: 10.1021/jacsau.5c00400. eCollection 2025 Jun 23.

Abstract

Hydrogen atom transfer (HAT) catalysis has emerged as a powerful tool for the C-H functionalization of organic molecules. While several HAT catalysts based on heteroatom-centered radicals have been developed, the study of the catalytic use of carbon-centered radicals responsible for the HAT process has been underexplored. Herein, we introduce phosphonium ylides as a HAT catalyst platform based on a carbon-centered radical. The readily available and highly tunable features of this platform have allowed the systematic study of the effect of the catalyst structure on its physical properties. The ability of these ylides as practical HAT catalysts has been demonstrated in the photoinduced C-H alkylation of various small organic molecules, including alcohols, heterocycles, and primary amines.

摘要

氢原子转移(HAT)催化已成为有机分子C-H官能团化的有力工具。虽然已经开发了几种基于以杂原子为中心的自由基的HAT催化剂,但对负责HAT过程的以碳为中心的自由基的催化用途的研究仍未充分探索。在此,我们引入磷叶立德作为基于以碳为中心的自由基的HAT催化剂平台。该平台易于获得且具有高度可调节性,使得能够系统地研究催化剂结构对其物理性质的影响。这些叶立德作为实用HAT催化剂的能力已在各种小分子有机化合物(包括醇、杂环和伯胺)的光诱导C-H烷基化反应中得到证明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1bb/12188387/6b7309330eff/au5c00400_0001.jpg

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