The Suzuki–Miyaura Reaction of BPin-substituted F-BODIPYs with Aryl Halides
| dc.contributor.author | Craig D. Smith | |
| dc.contributor.author | Alison Thompson | |
| dc.date.accessioned | 2025-07-28T17:20:26Z | |
| dc.date.available | 2025-07-28T17:20:26Z | |
| dc.date.issued | 2021-01-12 | |
| dc.description.abstract | F-BODIPYs substituted with BPin functionality have been coupled to aryl halides using a mild and efficient catalyst system involving Pd2(dba)3 and XPhos. The methodology enables the Suzuki–Miyaura cross-coupling of electron-rich, electron-poor, and sterically encumbered BPin-substituted F-BODIPYs to aryl halides bearing various functional groups, thus presenting an opportunity for the preparation of highly functionalised F-BODIPYs without need for the corresponding aryl moiety to be available in borylated form | |
| dc.identifier.citation | Published Version: Craig D. Smith and Alison Thompson. 2021. The Suzuki–Miyaura reaction of BPin-substituted F-BODIPYs with aryl halides. Canadian Journal of Chemistry. 99(3): 287-294. https://doi.org/10.1139/cjc-2020-0300 | |
| dc.identifier.uri | https://hdl.handle.net/10222/85241 | |
| dc.relation.ispartof | Canadian Journal of Chemistry | |
| dc.title | The Suzuki–Miyaura Reaction of BPin-substituted F-BODIPYs with Aryl Halides | |
| dc.type | Article |