光氧化还原β-C(sp3)-H通过HAT和双C-H功能化与杂芳烃的异芳化反应

Guang-Chuan Xu , Liang Zeng , Ming Hu , Fu-Jin Sun , Jin-Heng Li
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引用次数: 0

摘要

本研究报告介绍了一种有用的合成方法,即通过碘代芳香烃引导的光氧遥控 C(sp3)-H 杂芳香化邻碘芳香烃-1-酮与杂芳香烃的形式化β-杂芳香化酮。该方案依赖于单电子转移(SET)、氢原子转移(HAT)和双 C-H 功能化,从而得到 β-杂芳基酮。这种温和的方法具有广泛的适用范围、良好的官能团兼容性、高原子经济性和出色的选择性控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Photoredox β-C(sp3)–H heteroarylation of o-iodoaryl-alkan-1-ones with heteroarenes via HAT and dual C–H functionalizations†
A synthetically useful method for the formal β-heteroarylation of ketones via an iodoarene-directed photoredox remote C(sp3)–H heteroarylation of o-iodoarylalkan-1-ones with heteroarenes is reported. This protocol relies on single electron transfer (SET), hydrogen atom transfer (HAT) and dual C–H functionalizations leading to β-heteroaryl ketones. This mild method displays broad scope, good functional group compatibility, high atom economy and excellent selectivity control.
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