Photoredox Polyfluoroarylation of Alkyl Halides via Halogen Atom Transfer
dc.contributor.author | Niu, Ben | |
dc.contributor.author | Sachidanandan, Krishnakumar | |
dc.contributor.author | Blackburn, Bryan G. | |
dc.contributor.author | Cooke, Maria Victoria | |
dc.contributor.author | Laulhé, Sébastien | |
dc.contributor.department | Chemistry and Chemical Biology, School of Science | |
dc.date.accessioned | 2023-09-25T11:19:29Z | |
dc.date.available | 2023-09-25T11:19:29Z | |
dc.date.issued | 2022 | |
dc.description.abstract | Polyfluoroarene moieties are of interest in medicinal chemistry, agrochemicals, and material sciences. Herein, we present the first polyfluoroarylation of unactivated alkyl halides via a halogen atom transfer process. This method converts primary, secondary, and tertiary alkyl halides into the respective polyfluoroaryl compounds in good yields in the presence of amide, carbamate, ester, aromatic, and sulfonamide moieties, including derivatives of complex bioactive molecules. Mechanistic work revealed that this transformation proceeds through an alkyl radical generated after the halogen atom transfer. | |
dc.eprint.version | Author's manuscript | |
dc.identifier.citation | Niu B, Sachidanandan K, Blackburn BG, Cooke MV, Laulhé S. Photoredox Polyfluoroarylation of Alkyl Halides via Halogen Atom Transfer. Org Lett. 2022;24(3):916-920. doi:10.1021/acs.orglett.1c04267 | |
dc.identifier.uri | https://hdl.handle.net/1805/35737 | |
dc.language.iso | en_US | |
dc.publisher | American Chemical Society | |
dc.relation.isversionof | 10.1021/acs.orglett.1c04267 | |
dc.relation.journal | Organic Letters | |
dc.rights | Publisher Policy | |
dc.source | PMC | |
dc.subject | Halogens | |
dc.subject | Polyfluoroarene moieties | |
dc.subject | Polyfluoroarylation | |
dc.subject | Alkyl halides | |
dc.title | Photoredox Polyfluoroarylation of Alkyl Halides via Halogen Atom Transfer | |
dc.type | Article |