4.8 Article

Cobalt-Catalyzed Enantioselective Hydroarylation of 1,6-Enynes

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 142, 期 20, 页码 9510-9517

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AMER CHEMICAL SOC
DOI: 10.1021/jacs.0c03246

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资金

  1. University of Toronto
  2. Natural Science and Engineering Research Council (NSERC)
  3. Alphora/Eurofins
  4. Kennarshore, Inc.
  5. Walter C. Sumner Memorial Fellowship
  6. Province of Ontario
  7. Basque Government [IT908-16]
  8. UPV/EHU
  9. Government of Canada (NSERC-PGS)

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An asymmetric hydroarylative cyclization of enynes involving a C-H bond cleavage is reported. The cobalt-catalyzed cascade generates three new bonds in an atom-economical fashion. The products were obtained in excellent yields and excellent enantioselectivities as single diastereo- and regioisomers. Preliminary mechanistic studies indicate that the reaction shows no intermolecular C-H crossover. This work highlights the potential of cobalt catalysis in C-H bond functionalization and enantioselective domino reactivity.

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