4.8 Article

Catalytic Selenium-Promoted Intermolecular Friedel-Crafts Alkylation with Simple Alkenes

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ORGANIC LETTERS
卷 18, 期 5, 页码 912-915

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b03579

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  1. Ministry of Education of the People's Republic of China (Program for Changjiang Scholars and Innovative Research Team in University) [IRT13095]
  2. Natural Science Foundation of China [NSFC 21162032]

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A method for conducting selenium-promoted intermolecular Friedel-Crafts (F-C) alkylation reactions has been developed with simple alkenes using trimethylsilyl trifluoromethane-sulfonate as a catalyst and N-phenylselenophthalimide as an efficient selenium source. Electron-rich arenes smoothly underwent F-C alkylation with a variety of alkenes to afford alkylated products in good yield and with high regioselectivity and diastereoselectivity. The regioselectivity and stereoselectivity of arenes and alkenes as well as a preliminary mechanism of the F-C alkylation reaction are discussed.

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