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Metal-free three-component cyanoalkylation of quinoxalin-2(1<i>H</i>)-ones with vinylarenes and azobis(alkylcarbonitrile)s

Mayurakhi Bhuyan, Suraj Sharma, Gakul Baishya

2022Organic & Biomolecular Chemistry24 citationsDOI

Abstract

takes part in the reaction as a sole oxidant under base, additive, and metal-free conditions, producing the three-component products in moderate to good yields. The protocol also works with phenylacetylene in the absence of vinyl arenes and provides the respective product. Furthermore, different control experiments with radical scavengers like 2,2,6,6-tetramethylpiperidine-1-oxyl and diphenyl ethylene prove the generation of radicals during the reaction.

Topics & Concepts

ChemistryRadicalPhenylacetyleneComponent (thermodynamics)MetalBase (topology)Organic chemistryPolymer chemistryMedicinal chemistryCatalysisMathematicsMathematical analysisThermodynamicsPhysicsRadical Photochemical ReactionsSynthesis and Biological EvaluationOxidative Organic Chemistry Reactions
Metal-free three-component cyanoalkylation of quinoxalin-2(1<i>H</i>)-ones with vinylarenes and azobis(alkylcarbonitrile)s | Litcius