4.8 Article

A Stereoselective Arylative-Cyclopropanation Process

Journal

ORGANIC LETTERS
Volume 19, Issue 5, Pages 1188-1191

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b00248

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Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Canada Foundation for Innovation (CFI)
  3. provincial government of Quebec (FQRNT and CCVC)
  4. Programme Canadien de Bourses de la Francophonie

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A new stereoselective arylative cyclopropanation process involving treatment of halogenated dienone systems in the presence of a Michael donor containing a nitroaryl-sulfone has been developed. This transformation enables production of an arylated cyclopropane under mild conditions and occurs via a Michael Smiles ring closure cascade process, reflecting the concepts of green chemistry and atom economy.

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