6533b850fe1ef96bd12a81e3
RESEARCH PRODUCT
ChemInform Abstract: Synthesis of a Naphtho-pyrido-Annulated Iodonium Salt and Pd-Catalyzed Transformation to 7H-Naphtho[1,8-bc][1,5]naphthyridine.
Julien LetessierDieter SchollmeyerMario GeffeHeiner Detertsubject
chemistry.chemical_classificationTransformation (genetics)ChemistryNitroOrganic chemistrySalt (chemistry)General MedicineAminationCatalysisdescription
Nitropyridylnaphthalene is the central intermediate for the synthesis of naphthonaphthyridine and benzo-δ-carboline. Whereas the Cadogan reaction gives the carboline, transformation of the nitro group to iodo followed by oxidation and cyclization results in an iodonium salt. A twofold Pd-catalyzed amination leads to the naphthyridine.
year | journal | country | edition | language |
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2014-04-17 | ChemInform |