Synthetic Communications · 1999 · 16 citations · 7 references
Natural SciencesChemistryMedicinal ChemistryOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic Synthesis1, 3-Dipolar CycloadditionIsoquinoline ChemistryIsoquinoline SynthesisNitrile Oxide CycloadditionQuinoline ChemistryQuinoline Synthesis
Abstract Condensation of 2-chloro-3-formylquinoline 1a-c with allylthiol 2 afforded 2-allysulfanyl-3-formylquinolines 3a-c. Oximation followed by oxidation of 3a-c with NaOCl or chloramine-T, in cold or mercuric acetate resulted in the formation of respective nitrile oxides, which underwent insituintramolecular 1,3-dipolar cycloaddition reaction and afforded the title compounds 5a-c in high yield.
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Otto Meth‐Cohn, Bramha Narine, B. TARNOWSKI et al. · Journal of the Chemical Society Perkin Transactions 1 · 1981 · 70 citations