Efficient access to chromeno[4,3-b]quinolines related to dependensin

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dc.contributor.authorDobrowolski, JCen_AU
dc.contributor.authorFraser, BHen_AU
dc.contributor.authorBhadbhade, MMen_AU
dc.contributor.authorBlack, DSen_AU
dc.contributor.authorKumar, Nen_AU
dc.date.accessioned2021-08-10T06:45:27Zen_AU
dc.date.available2021-08-10T06:45:27Zen_AU
dc.date.issued2017-08-08en_AU
dc.date.statistics2021-08-10en_AU
dc.description.abstractWe report a robust synthesis of novel chromeno[4,3-b]quinoline derivatives structurally similar to the natural product dependensin. The target compounds are accessed through the acid-catalysed condensation of 2-aminoacetophenones or 2-aminochalcones with substituted flavanones, which are in turn obtained from 2-hydroxyacetophenones and benzaldehydes. © 2017 Georg Thieme Verlag Stuttgarten_AU
dc.identifier.citationDobrowolski, J. C., Fraser, B. H., Bhadbhade, M., Black, D. S., & Kumar, N. (2017). Efficient access to chromeno[4,3-b]quinolines related to dependensin. Synlett, 28(15), 1979-1983. doi:10.1055/s-0036-1589087en_AU
dc.identifier.issn1437-2096en_AU
dc.identifier.issue15en_AU
dc.identifier.journaltitleSynletten_AU
dc.identifier.pagination1979-1983en_AU
dc.identifier.urihttps://doi.org/10.1055/s-0036-1589087en_AU
dc.identifier.urihttps://apo.ansto.gov.au/dspace/handle/10238/11295en_AU
dc.identifier.volume28en_AU
dc.language.isoenen_AU
dc.publisher© Georg Thieme Verlag Stuttgarten_AU
dc.subjectQuinolinesen_AU
dc.subjectSynthesisen_AU
dc.subjectBenzaldehydeen_AU
dc.subjectDehydrocyclizationen_AU
dc.subjectMoleculesen_AU
dc.subjectFlavonoidsen_AU
dc.titleEfficient access to chromeno[4,3-b]quinolines related to dependensinen_AU
dc.typeJournal Articleen_AU
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