4.8 Article

Asymmetric Allylic C-H Alkylation via Palladium(II)/cis-ArSOX Catalysis

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 140, Issue 34, Pages 10658-10662

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b05668

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Funding

  1. NIGMS MIRA [R35 GM122525]
  2. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R35GM122525] Funding Source: NIH RePORTER

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We report the development of Pd(II)/cis-aryl sulfoxide-oxazoline (cis-ArSOX) catalysts for asymmetric C-H alkylation of terminal olefins with a variety of synthetically versatile nucleophiles. The modular, tunable, and oxidatively stable ArSOX scaffold is key to the unprecedented broad scope and high enantioselectivity (37 examples, avg. > 90% ee). Pd(II)/cis-ArSOX is unique in its ability to effect high reactivity and catalyst-controlled diastereoselectivity on the alkylation of aliphatic olefins. We anticipate that this new chiral ligand class will find use in other transition metal catalyzed processes that operate under oxidative conditions.

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