4.8 Article

Copper-Catalyzed Hydroarylation of Internal Alkynes: Highly Regio- and Diastereoselective Synthesis of 1,1-Diaryl, Trisubstituted Olefins

期刊

ACS CATALYSIS
卷 7, 期 9, 页码 6220-6224

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.7b01847

关键词

copper; C-C coupling; alkynes; arenes; synthetic methods

资金

  1. University of Illinois
  2. NSF CAREER [1555337]
  3. Direct For Mathematical & Physical Scien
  4. Division Of Chemistry [1555337] Funding Source: National Science Foundation

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The copper-catalyzed hydroarylation of internal, unsymmeric alkynes is presented. Trisubstituted alkenes are obtained as single diastereomers in good to excellent yields and excellent regioselectivities. The scope of the reaction is presented with respect to alkyne and aryl iodide coupling partners. Initial mechanistic experiments indicate a hydrocupration event followed by a two-electron oxidative addition/reductive elimination pathway.

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