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RESEARCH PRODUCT
Electrochemical oxidation of substituted pyrroles.III.Anodic oxidation of 2,5-diphenyl-3-acetylpyrrole
Salvatore PetrusoGiuseppe FilardoGiuseppe SilvestriS. CaronnaSalvatore Gambinosubject
Indole testChemistryOrganic Chemistrychemistry.chemical_elementZincElectrochemistryMedicinal chemistrychemistry.chemical_compoundTransition metalYield (chemistry)Organic chemistryCyclic voltammetryAcetonitrileDerivative (chemistry)description
The electrochemical oxidation of 2,5-diphenyl-3-acetylpyrrole (I) is described. The cyclic derivative 1,6a-dihydro-2,5,6a-triphenyl-3,4-diacetylbenzo[g]pyrrolo[3,2-e]indole (II) was obtained in very good yield. However, when water was present in the reaction medium, a different derivative, 4-acetyl-2-hydroxy-2,5-diphenyl-3-(4′-acetyl-2′,5′-diphenyl-3′-yl)-2H-pyrrole (III), was obtained as the main product. 2,2′,5,5′-Tetraphenyl-4,4′-diacetyl-3,3′-dipyrryl (IV), a potentially useful intermediate for the synthesis of condensed pyrroles, was synthesized by zinc reduction of III.
year | journal | country | edition | language |
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1991-04-01 | Journal of Heterocyclic Chemistry |