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Photo-induced energy transfer relay of N-heterocyclic carbene catalysis: an asymmetric α-fluorination/isomerization cascade

Xinhang Jiang, En Li, Jiean Chen, Yong Huang

2020Chemical Communications30 citationsDOI

Abstract

The geometric configuration of olefin products is often driven by thermodynamic control in synthesis. Methods enabling switching of cis/trans selectivity are rare. Recently, photosensitized approaches have emerged as a powerful tool for accomplishing this task. In this report, we report an in situ isomerization of an N-heterocyclic carbene (NHC)-bound intermediate by a photo-induced energy transfer process that leads to selective access of chiral allylic fluorides with a cis-olefin geometry. In the absence of a photocatalyst or light, the reaction proceeds smoothly to give (E)-olefin products, while the (Z)-isomer can be obtained under photosensitizing conditions. Preliminary mechanistic experiments suggest that an energy transfer process might be operative.

Topics & Concepts

IsomerizationCascadeCarbeneRelayCatalysisOlefin fiberChemistryEnergy transferPhotochemistryCombinatorial chemistryComputational chemistryChemical physicsOrganic chemistryPhysicsThermodynamicsChromatographyPower (physics)Fluorine in Organic ChemistryN-Heterocyclic Carbenes in Organic and Inorganic ChemistryCyclopropane Reaction Mechanisms
Photo-induced energy transfer relay of N-heterocyclic carbene catalysis: an asymmetric α-fluorination/isomerization cascade | Litcius