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RESEARCH PRODUCT
Polycondensed nitrogen heterocycles. Part 23. Pyrrolo[3,2-c]cinnolines by a japp-klingemann type reaction
Anna Maria AlmericoGaetano DattoloGirolamo CirrincioneEnrico Aiellosubject
Intramolecular reactionJapp–Klingemann reactionOrganic ChemistryHalogenationchemistry.chemical_elementMedicinal chemistryIonchemistry.chemical_compoundchemistryIntramolecular forceChlorineOrganic chemistryCinnolinePyrroledescription
Pyrrolo[3,2-c]cinnoline derivatives were obtained by an unusual Japp-Klingemann reaction involving an intramolecular azadehalogenation on the pyrrole nucleus. Such an azadehalogenation represents the first example of Japp-Klingemann reaction in which the extrusion of positive chlorine ion is verified.
year | journal | country | edition | language |
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1990-05-01 | Journal of Heterocyclic Chemistry |