4.8 Article

Synthesis of Bidentate Nitrogen Ligands by Rh-Catalyzed C-H Annulation and Their Application to Pd-Catalyzed Aerobic C-H Alkenylation

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ORGANIC LETTERS
卷 23, 期 9, 页码 3657-3662

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.1c01040

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  1. National Research Foundation of Korea [NRF-2019R1A2C1007852, NRF-2019R1A4A1028007]

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A new class of bidentate ligands was synthesized through a modular approach involving Rh-catalyzed reactions. These ligands enable Pd-catalyzed C-H alkenylation on electron-rich and sterically less hindered arenes, while facilitating the oxidation of Pd(0) intermediates, potentially finding broad application in transition-metal-catalyzed reactions.
A new class of bidentate ligands was prepared by a modular approach involving Rh-catalyzed C-H annulation reactions. The resulting conformationally constrained ligands enabled the Pd-catalyzed C-H alkenylation at electron-rich and sterically less hindered positions of electron-rich arenes while promoting the facile oxidation of Pd(0) intermediates by oxygen. This newly introduced ligand class is complementary to the ligands developed for Pd-catalyzed oxidative reactions and may find broad application in transition-metal-catalyzed reactions.

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