4.8 Article

Chiral Diene as the Ligand for the Synthesis of Axially Chiral Compounds via Palladium-Catalyzed Suzuki-Miyaura Coupling Reaction

Journal

ORGANIC LETTERS
Volume 12, Issue 23, Pages 5546-5549

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol102521q

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Funding

  1. Major State Basic Research Development Program [2010CB833302]
  2. Chinese Academy of Sciences [KJCX2-YW-11-07]
  3. Shanghai Municipal Committee of Science and Technology [09JC1417300]

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The first palladium-diene-catalyzed asymmetric Suzuki-Miyaura coupling reaction has been achieved. A number of functionalized biaryls were obtained in high yields and in moderate to high enantioselectivities. The existence of an ortho-formyl group greatly improves the catalyst efficiency and permits further synthetic elaborations.

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