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Photoredox/Nickel Dual-Catalytic Asymmetric Silylarylation of Alkenes. | LitMetric

Photoredox/Nickel Dual-Catalytic Asymmetric Silylarylation of Alkenes.

Org Lett

Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, Shanghai Key Laboratory of New Drug Design, and School of Pharmacy, East China University of Science and Technology, Shanghai 200237, P. R. China.

Published: January 2025

The efficient construction of chiral aryl-containing organosilicon frameworks via catalytic enantioselective three-component silylarylation of alkenes remains a great challenge. Herein, a photoredox/nickel dual-catalytic asymmetric protocol has been disclosed by using a chiral biimidazoline (BiIM) as the ligand, silylboranes as the silyl radical precursors, aryl bromides as the coupling partners, and morpholine as the promoter. Remarkably, the reaction features mild and green conditions, high reaction efficiency, and excellent enantioselectivity, enabling the facile synthesis of valuable chiral tropic acid and sila-isoflavanone structures.

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Source
http://dx.doi.org/10.1021/acs.orglett.4c04570DOI Listing

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