Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2901
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dc.contributor.authorKhullar, S.-
dc.contributor.authorMandal, S.K.-
dc.date.accessioned2020-12-09T09:20:10Z-
dc.date.available2020-12-09T09:20:10Z-
dc.date.issued2014-
dc.identifier.citationChemical Communications,50(70), pp.10078-10081.en_US
dc.identifier.otherhttps://doi.org/10.1039/C4CC03079F-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2014/CC/C4CC03079F#!divAbstract-
dc.identifier.urihttp://hdl.handle.net/123456789/2901-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractA one pot domino protocol for an efficient synthesis of 7-arylbenzo[c]acridine-5,6-diones, with a novel nucleus, has been developed by reacting 2-hydroxynaphthalene-1,4-dione, aromatic aldehydes and aromatic amines using environmentally benevolent p-toluene sulphonic acid as a catalyst. An exciting feature of this communication is the reaction mechanism that depends on the reaction solvent.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subject5,6-dionesen_US
dc.subjectHydroxynaphthaleneen_US
dc.subjectp-toluene sulphonic aciden_US
dc.titleA one-pot, three-component reaction for the synthesis of novel 7-arylbenzo[c]acridine-5,6-dionesen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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