Publication | Closed Access
Aromatization-Driven Cascade [1,5]-Hydride Transfer/Spirocyclization Promoted by Fluorinated Alcohols
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Citations
87
References
2019
Year
Aromatization-driven Redox-neutral CascadeEngineeringOrtho-benzylated AnilinesHeterocyclicAlkene MetathesisOrganic ChemistryCatalysisChemistryHeterocycle ChemistryPharmacologySynthetic ChemistryPara-quinone MethideFluorinated Alcohols
The aromatization-driven redox-neutral cascade [1,5]-hydride transfer/spirocyclization and cascade [1,5]-hydride transfer/hydrolysis from para-quinone methide in HFIP were developed. These protocols enabled the synthesis of azaspirocyclohexadienones and ortho-benzylated anilines in good to high yields under mild conditions, featuring room temperature, additive-free, and good functional group tolerance.
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