A general and efficient synthesis of 5,6-dihydrodibenzo[b,h][1,6]naphthyridine derivatives

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dc.contributor.authorDobrowolski, JCen_AU
dc.contributor.authorKaten, Aen_AU
dc.contributor.authorFraser, BHen_AU
dc.contributor.authorBhadbhade, MMen_AU
dc.contributor.authorBlack, DSen_AU
dc.contributor.authorKumar, Nen_AU
dc.date.accessioned2021-08-11T05:25:07Zen_AU
dc.date.available2021-08-11T05:25:07Zen_AU
dc.date.issued2016-12-07en_AU
dc.date.statistics2021-08-10en_AU
dc.description.abstractA two-step procedure for the synthesis of dihydrodibenzonaphthyridine derivatives from benzaldehydes and 2-aminoacetophenones, proceeding through a substituted dihydroquinolone intermediate, is described. The synthetic protocol allows for a versatile and robust coupling method between a range of 2-aminoacetophenones or 2-aminobenzophenones and a selection of substituted dihydroquinolones. © 2016 Elsevier B.V.en_AU
dc.identifier.citationDobrowolski, J. C., Katen, A., Fraser, B. H., Bhadbhade, M., Black, D. S., & Kumar, N. (2016). A general and efficient synthesis of 5,6-dihydrodibenzo[b,h][1,6]naphthyridine derivatives. Tetrahedron Letters, 57(49), 5442-5445. doi:10.1016/j.tetlet.2016.10.067en_AU
dc.identifier.issn0040-4039en_AU
dc.identifier.issue49en_AU
dc.identifier.journaltitleTetrahedron Lettersen_AU
dc.identifier.pagination5442-5445en_AU
dc.identifier.urihttps://doi.org/10.1016/j.tetlet.2016.10.067en_AU
dc.identifier.urihttps://apo.ansto.gov.au/dspace/handle/10238/11328en_AU
dc.identifier.volume57en_AU
dc.language.isoenen_AU
dc.publisherElsevier B. V.en_AU
dc.subjectSynthesisen_AU
dc.subjectDerivatizationen_AU
dc.subjectChemical reactionsen_AU
dc.subjectBenzaldehydeen_AU
dc.subjectFlavonoidsen_AU
dc.subjectMalariaen_AU
dc.subjectNitrogenen_AU
dc.titleA general and efficient synthesis of 5,6-dihydrodibenzo[b,h][1,6]naphthyridine derivativesen_AU
dc.typeJournal Articleen_AU
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