Aryl-Radical-Initiated <i>Z</i>‑OlefinSynthesis via Synergistic Palladium and Photocatalysis

We report a novel photocatalyzed selective functionalization of terminal olefins for the synthesis of <i>Z</i>-olefins and cyclobutanes under mild conditions in excellent yields. A series of <i>Z</i>-cinnamic acid derivatives, enamines, and amide-containing cyclobutanes were efficiently synthesized using this method. Mechanistic studies indicated that the success of this reaction is based on the triple radical relay strategy, anion−π interaction for aryl halide activation and aryl radical generation, palladium for controlling chemoselectivity of the aryl radical, and photocatalyst for controlling stereoselectivity via diradical species, respectively.

Publication Details

Journal
Figshare
Published
2025-02-07
DOI
https://doi.org/10.1021/acs.orglett.5c00073.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
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Aryl-Radical-Initiated Z‑OlefinSynthesis via Synergistic Palladium and Photocatalysis

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Mycorrhizal Fungi and Plant Interactions
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Aryl-Radical-Initiated Z‑OlefinSynthesis via Synergistic Palladium and Photocatalysis

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Abstract

We report a novel photocatalyzed selective functionalization of terminal olefins for the synthesis of <i>Z</i>-olefins and cyclobutanes under mild conditions in excellent yields. A series of <i>Z</i>-cinnamic acid derivatives, enamines, and amide-containing cyclobutanes were efficiently synthesized using this method. Mechanistic studies indicated that the success of this reaction is based on the triple radical relay strategy, anion−π interaction for aryl halide activation and aryl radical generation, palladium for controlling chemoselectivity of the aryl radical, and photocatalyst for controlling stereoselectivity via diradical species, respectively.

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Mycorrhizal Fungi and Plant Interactions
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Aryl-Radical-Initiated <i>Z</i>‑OlefinSynthesis via Synergistic Palladium and Photocatalysis · Figshare (2025) | TGRS Research Map | TGRS