Iridium‐Catalyzed Regio‐ and Enantioselective Hydroarylation of Alkenyl Ethers by Olefin Isomerization

Iridium‐catalyzed hydroarylation of alkenyl ethers, such as allylic and homoallylic ethers, by C−H bond activation gave high yields of the corresponding addition products, where the aryl groups were selectively installed at the α‐carbon atom to the alkoxy group. The reaction involves an isomerizatio...

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Veröffentlicht in:Angewandte Chemie International Edition 2017-05, Vol.56 (20), p.5607-5611
Hauptverfasser: Ebe, Yusuke, Onoda, Mitsuki, Nishimura, Takahiro, Yorimitsu, Hideki
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Sprache:eng
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Zusammenfassung:Iridium‐catalyzed hydroarylation of alkenyl ethers, such as allylic and homoallylic ethers, by C−H bond activation gave high yields of the corresponding addition products, where the aryl groups were selectively installed at the α‐carbon atom to the alkoxy group. The reaction involves an isomerization of the alkenyl ethers into the corresponding 1‐alkenyl ethers, which then undergo the regio‐ and enantioselective hydroarylation. Chain walking: Iridium‐catalyzed hydroarylation of alkenyl ethers, such as allylic and homoallylic ethers, by C−H bond activation gave high yields of the corresponding addition products. The aryl groups were selectively installed at the α‐carbon atom to the alkoxy group. ArF=3,5‐(CF3)2C6H3.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201702286