A Stereoselective Arylative-Cyclopropanation Process.
Siomenan CoulibaliElsa DeruerElizabeth GodinSylvain CanesiPublished in: Organic letters (2017)
A new stereoselective arylative cyclopropanation process involving treatment of halogenated dienone systems in the presence of a Michael donor containing a nitro-aryl-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.