4.8 Article

Enantioselective, Nickel-Catalyzed Suzuki Cross-Coupling of Quinolinium Ions

Journal

ORGANIC LETTERS
Volume 16, Issue 1, Pages 142-145

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol4031364

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Funding

  1. NIGMS [R01 GM100985-01]
  2. Princeton University
  3. Eli Lilly
  4. Amgen

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Quinolinium ions are engaged in an asymmetric, Ni-catalyzed Suzuki cross-coupling to yield 2-aryl- and 2-heteroaryl-1,2-dihydroquinolines. Key to the development of this method is the use of a Ni(II) precatalyst that activates without the need for strong reductants or high temperatures. The Ni-iminium activation mode is demonstrated as an exceptionally mild pathway to generate enantioenriched products from racemic starting materials.

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