4.8 Article

Copper-Catalyzed Dicarbofunctionalization of Unactivated Olefins by Tandem Cyclization/Cross-Coupling

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 139, 期 16, 页码 5700-5703

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AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b01922

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  1. University of New Mexico (UNM)
  2. National Science Foundation [NSF CHE-1554299]
  3. NSF [CHE08-40523, CHE09-46690]
  4. NSF CRIF:MU award [CHE04-43580]

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We present a strategy that difunctionalizes unactivated olefins in 1,2-positions with two carbon-based entities. This method utilizes alkyl/arylzinc reagents derived from olefin-tethered alkyl/aryl halides that undergo radical cyclization to generate C(sp(3))-Cu complexes in situ, which are intercepted with aryl and heteroaryl iodides. A variety of (arylmethyl)carbo- and heterocycles (N, O) can be synthesized with this new method.

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