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Electrochemical Synthesis of Spiro[4.5]trienones through Radical‐Initiated Dearomative Spirocyclization

Jiawei Hua, Zheng Fang, Mixue Bian, Tao Ma, Man Yang, Jia Xu, Chengkou Liu, Wei He, Ning Zhu, Zhao Yang, Kai Guo

2020ChemSusChem90 citationsDOI

Abstract

A novel and green route has been developed for the electrochemical synthesis of spiro[4.5]trienones through radical-initiated dearomative spirocyclization of alkynes with diselenides. This metal-free and oxidant-free electrosynthesis reaction was performed in an undivided cell under mild conditions. A variety of selenation spiro[4.5]trienones products were prepared in moderate-to-good yields, showing a broad scope and functional group tolerance. Moreover, the developed continuous-flow system combined with electrosynthesis possesses the potential to achieve scaled-up reactions, overcoming the low efficiency of conventional electrochemical scaled-up reactions.

Topics & Concepts

ElectrosynthesisElectrochemistryCombinatorial chemistryChemistryReaction conditionsFunctional groupOrganic chemistryCatalysisPhysical chemistryElectrodePolymerSulfur-Based Synthesis TechniquesRadical Photochemical ReactionsCatalytic C–H Functionalization Methods
Electrochemical Synthesis of Spiro[4.5]trienones through Radical‐Initiated Dearomative Spirocyclization | Litcius