Publication | Closed Access
Metal-free TBAI-catalyzed arylsulfonylation of activated alkenes with sulfonylhydrazides
59
Citations
47
References
2015
Year
Sulfonyl RadicalsChemical EngineeringDerivativesEngineeringOrganic ChemistryCorresponding Isoquinoline-1,3CatalysisChemistry-Dione DerivativesAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisMetal-free Tbai-catalyzed Arylsulfonylation
An efficient metal-free oxidative arylsulfonylation of α,β-unsaturated imides with sulfonylhydrazides leading to isoquinoline-1,3(2H,4H)-dione derivatives has been developed. The procedure involves the generation of sulfonyl radicals via cleavage of the S-N bond of sulfonylhydrazides with sulfonylation and C-H functionalization. The protocol uses the economical and environmentally friendly TBAI-TBHP catalytic system, and the corresponding isoquinoline-1,3(2H,4H)-diones with various functional groups were obtained in moderate to good yields.
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