| Literature DB >> 33530687 |
Kalipada Jana1, Isao Mizota1, Armido Studer1.
Abstract
Formal hydroperfluoroalkylation of enones is achieved in a two-step process comprising conjugate hydroboration and subsequent radical perfluoroalkylation. The 1,4-hydroboration of the enone is conducted in the absence of any transition metal catalyst with catecholborane in 1,2-dichloroethane, and the generated boron enolate is in situ α-perfluoroalkylated with a perfluoroalkyl iodide upon blue LED irradiation in the presence of an amine additive. Both reactions proceed under very mild conditions at room temperature.Entities:
Year: 2021 PMID: 33530687 DOI: 10.1021/acs.orglett.0c04260
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005