4.8 Article

Pd-Catalyzed Alkene Difunctionalization Reactions of Malonate Nucleophiles: Synthesis of Substituted Cyclopentanes via Alkene Aryl-Alkylation and Akenyl-Alkylation

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ORGANIC LETTERS
卷 21, 期 10, 页码 3813-3816

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b01258

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  1. NIH-NIGMS [GM 124030]
  2. University of Michigan Rackham dissertation fellowship

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The Pd-catalyzed coupling of malonate nucleophiles with alkenes bearing tethered aryl or alkenyl triflates is described. These alkene difunctionalization reactions afford malonate-substituted cyclopentanes that contain fused aryl or cycloalkenyl rings. The transformations generate a five-membered ring, two C-C bonds, and provide products bearing up to three stereocenters with good chemical yield and generally high diastereoselectivity.

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