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Ni-catalyzed hydroarylation of alkynes with unactivated β-C(sp2)−H bonds

Shao-Long Qi, Yu-Peng Liu, Yi Li, Yu-Xin Luan and Mengchun Ye ()
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Shao-Long Qi: State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University
Yu-Peng Liu: State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University
Yi Li: State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University
Yu-Xin Luan: State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University
Mengchun Ye: State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University

Nature Communications, 2022, vol. 13, issue 1, 1-9

Abstract: Abstract Hydroarylation of alkynes with unactivated C(sp2)−H bonds via chelated C−H metalation mainly occurs at γ-position to the coordinating atom of directing groups via stable 5-membered metallacycles, while β-C(sp2)−H bond-involved hydroarylation has been a formidable challenge. Herein, we used a phosphine oxide-ligated Ni−Al bimetallic catalyst to enable β-C−H bond-involved hydroarylations of alkynes via a rare 7-membered nickelacycle.

Date: 2022
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DOI: 10.1038/s41467-022-30367-8

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