4.8 Article

Development and Analysis of a Pd(0)-Catalyzed Enantioselective 1,1-Diarylation of Acrylates Enabled by Chiral Anion Phase Transfer

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 138, 期 49, 页码 15877-15880

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AMER CHEMICAL SOC
DOI: 10.1021/jacs.6b11367

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资金

  1. NIH [R01GM063540]
  2. NSF [CHE-1361296]
  3. JSPS KAKENHI [26.2447]
  4. Ermenegildo Zegna Group
  5. Division Of Chemistry
  6. Direct For Mathematical & Physical Scien [1361296] Funding Source: National Science Foundation

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Enantioselective 1,1-diarylation of terminal alkenes enabled by the combination of Pd catalysis with a chiral anion phase transfer (CAPT) strategy is reported herein. The reaction of substituted benzyl acrylates with aryldiazonium salts and arylboronic acids gave the corresponding 3,3-diarylpropanoates in moderate to good yields with high enantioselectivies (up to 98:2 er). Substituents on the benzyl acrylate and CAPT catalyst significantly affect the enantioselectivity, and multidimensional parametrization identified correlations suggesting structural origins for the high stereocontrol.

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