Difunctionalization of olefins represents a powerful synthetic tool and yet a challenging task. This work describes an electrochemically enabled fluoroalkylation-migration reaction of unactivated olefins in the absence of a strong oxidant or heavy metal catalyst, affording fluorinated (hetero)aryl ketones in good yields and excellent regioselectivities. The efficient and sustainable electrochemical strategy provides a rapid access to a dual functionalized fluorine-containing heterocyclic manifold.
Keyphrases
- heavy metals
- ionic liquid
- molecularly imprinted
- gold nanoparticles
- room temperature
- positron emission tomography
- risk assessment
- quantum dots
- reduced graphene oxide
- health risk
- health risk assessment
- minimally invasive
- highly efficient
- electron transfer
- pet imaging
- metal organic framework
- loop mediated isothermal amplification
- label free
- anti inflammatory
- carbon dioxide
- sewage sludge
- computed tomography
- mass spectrometry
- anaerobic digestion