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dc.contributor.authorParvatkar, P.T.
dc.contributor.authorMajik, M.S.
dc.date.accessioned2015-11-06T05:52:50Z
dc.date.available2015-11-06T05:52:50Z
dc.date.issued2014
dc.identifier.citationRSC Advances, vol.4; 2014; 22481-22486.
dc.identifier.urihttp://drs.nio.org/drs/handle/2264/4855
dc.description.abstractSynthesis of two linear indoloquinolines i.e. 6H-indolo[2,3-b]quinoline & 11-hydroxy-10H-indolo[3,2-b]quinoline, and spiro[2H-indole-2,3'-oxindole] from a common intermediate, (2-nitrophenyl)methylidene-dihydro-indolone derivative is described using microwave-mediated reductive cyclization as the key step.
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.rightsAn edited version of this paper was published by and © The Royal Society of Chemistry 2014. http://dx.doi.org/10.1039/c4ra02814g
dc.subjectSynthesis
dc.subjectcyclization
dc.titleMicrowave-assisted reductive cyclization: An easy entry to the indoloquinolines and spiro[2H-indole-2,30-oxindole].
dc.typeJournal Article


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