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![[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F59739.jpg&w=3840&q=50)
[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
Published on: May 21, 2019
Photoredox radical/polar crossover enables C-H
1School of Chemistry, Sun Yat-Sen University Panyu District Guangzhou 510006 China zhoul39@mail.sysu.edu.cn.
Abstract:
A photocatalytic C-H gem-difunctionalization of 1,3-benzodioxoles with two different alkenes for the synthesis of highly functionalized monofluorocyclohexenes is described. Using 4CzIPN as the photocatalyst, the direct single electron oxidation of 1,3-benzodioxoles allows their defluorinative coupling with α-trifluoromethyl alkenes to produce gem-difluoroalkenes in a redox-neutral radical polar crossover manifold. The C-H bond of the resultant γ,γ-difluoroallylated 1,3-benzodioxoles was further functionalized via radical addition to electron-deficient alkenes using a more oxidizing iridium photocatalyst. The capture of in situ generated carbanions by an electrophilic gem-difluoromethylene carbon and consecutive β-fluoride elimination afford monofluorocyclohexenes. The synergistic combination of multiple termination pathways of carbanions enables rapid incorporation of molecular complexity via stitching simple and readily accessible starting materials together.
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