4.8 Article

Stereospecific Cross-Coupling of Secondary Alkyl β-Trifluoroboratoamides

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 132, 期 48, 页码 17108-17110

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AMER CHEMICAL SOC
DOI: 10.1021/ja108949w

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资金

  1. NCRR NIH HHS [S10 RR016640-01] Funding Source: Medline
  2. NIGMS NIH HHS [R01 GM035249, GM035249, R01 GM035249-25] Funding Source: Medline
  3. Division Of Chemistry
  4. Direct For Mathematical & Physical Scien [0848460] Funding Source: National Science Foundation

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The stereospecific cross-coupling of enantioenriched nonbenzylic secondary alkyl boron compounds has been achieved. The high selectivity toward product formation over an undesired beta-H elimination pathway is achieved via an intramolecular coordination of an ancillary carbonyl to the metal center in the diorganopalladium intermediate.

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