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PCET-Mediated Ring-Opening Alkenylation of Cycloalkanols via Dual Photoredox and Cobalt Catalysis
The construction of molecular skeletons and modification of molecules using widely available and easily prepared alcohols as radical precursors for coupling reactions are significant and challenging subjects. We herein report a straightforward strategy for the dehydrogenative ring-opening alkenylati...
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Published in: | Organic letters 2023-01, Vol.25 (1), p.93-98 |
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container_title | Organic letters |
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creator | Ren, Zi-Gang Yu, Wan-Lei Zheng, Hai-Xue Xu, Peng-Fei |
description | The construction of molecular skeletons and modification of molecules using widely available and easily prepared alcohols as radical precursors for coupling reactions are significant and challenging subjects. We herein report a straightforward strategy for the dehydrogenative ring-opening alkenylation of cycloalkanols with alkenes by combining a proton-coupled electron transfer strategy and a dual photoredox and cobalt catalysis system. With this approach, a series of distally unsaturated ketones were obtained in 17–83% yields with high E selectivity. |
doi_str_mv | 10.1021/acs.orglett.2c03894 |
format | article |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Alcohols Alkenes Catalysis Cobalt Electron Transport Humans Protons |
title | PCET-Mediated Ring-Opening Alkenylation of Cycloalkanols via Dual Photoredox and Cobalt Catalysis |
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