| Literature DB >> 28205443 |
Siomenan Coulibali1, Elsa Deruer1, Elizabeth Godin1, Sylvain Canesi1.
Abstract
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.Entities:
Year: 2017 PMID： 28205443 DOI： 10.1021/acs.orglett.7b00248
Source DB: PubMed Journal: Org Lett ISSN： 1523-7052 Impact factor: 6.005