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Photoinduced, Redox-Neutral Decyanative and Defluorinative Phosphination of (Hetero)Arenes.

作者信息

Wang Conghui, Tang Meizhong, Wang Yating, Huang Shenlin, Xie Lan-Gui

机构信息

National and Local Joint Engineering Research Center of Biomedical Functional Materials, Jiangsu Key Laboratory of New Power Batteries, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210023, China.

Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, College of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, China.

出版信息

Org Lett. 2024 Sep 27;26(38):8154-8158. doi: 10.1021/acs.orglett.4c03049. Epub 2024 Sep 16.

DOI:10.1021/acs.orglett.4c03049
PMID:39283008
Abstract

Triarylphosphines play a crucial role in organic synthesis as versatile components serving as ligands, catalysts, and reactants. This study introduces a metal-free, visible-light-induced method for the cross-coupling of cyanopyridines or polyfluoroarenes with diarylphosphines. This approach facilitates the formation of C(sp)-P bonds through redox-neutral decyanative or defluorinative process, enabling the convenient synthesis of diverse triarylphosphines.

摘要

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