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原位烷基自由基循环驱动的解耦电化学脱氨反应

In Situ Alkyl Radical Recycling-Driven Decoupled Electrophotochemical Deamination.

作者信息

Wang Kui, Liu Xiaoyu, Yang Siyu, Tian Yan, Zhou Mingyang, Zhou Jianhua, Jia Xiaofei, Li Baoying, Liu Siyuan, Chen Jianbin

机构信息

Shandong Provincial Key Laboratory of Molecular Engineering, State Key Laboratory of Biobased Material and Green Papermaking, School of Chemistry and Chemical Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, People's Republic of China.

Key Laboratory of Optic-electric Sensing and Analytical Chemistry for Life Science, MOE, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, People's Republic of China.

出版信息

Org Lett. 2022 May 20;24(19):3471-3476. doi: 10.1021/acs.orglett.2c01022. Epub 2022 May 12.

Abstract

Molecular electrophotocatalysis has emerged as a powerful strategy for the development of sustainable synthetic protocols. With the proof-of-concept, we exploited a versatile electrophotocatalytic deaminative alkylation approach. Mechanistic investigation indicated that in situ recycling of the alkyl radicals was the key point. Notably, ligand modification and late-stage functionalization of pharmaceuticals were also established, highlighting its feasibility in practical utilization.

摘要

分子光电催化已成为开发可持续合成方法的有力策略。基于概念验证,我们开发了一种通用的光电催化脱氨基烷基化方法。机理研究表明,烷基自由基的原位循环是关键。值得注意的是,还实现了配体修饰和药物的后期功能化,突出了其在实际应用中的可行性。

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