Publication | Closed Access
Visible-Light-Mediated C–I Difluoroallylation with an α-Aminoalkyl Radical as a Mediator
54
Citations
28
References
2021
Year
Room TemperatureMedicinal ChemistryDerivativesEngineeringPhotochemistryNatural SciencesMechanistic PhotochemistryDiversity-oriented SynthesisRadical (Chemistry)Fluorous SynthesisMild ProtocolOrganic ChemistrySynthetic PhotochemistryInexpensive MediatorChemistryVisible-light-mediated C–i DifluoroallylationPhotophysical PropertyBiomolecular Engineering
Herein, we report a protocol for direct visible-light-mediated C-I difluoroallylation reactions of α-trifluoromethyl arylalkenes with alkyl iodides at room temperature with an α-aminoalkyl radical as a mediator. The protocol permits efficient functionalization of various α-trifluoromethyl arylalkenes with cyclic and acyclic primary, secondary, and tertiary alkyl iodides and is scalable to the gram level. This mild protocol uses an inexpensive mediator and is suitable for late-stage functionalization of complex natural products and drugs.
| Year | Citations | |
|---|---|---|
Page 1
Page 1