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Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/67340
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dc.contributor.authorRubina Muniren_US
dc.contributor.authorMuhammad Makshoof Athaen_US
dc.contributor.authorMuhammad Zia-ur-Rehmanen_US
dc.contributor.authorNoman Javiden_US
dc.date.accessioned2020-04-02T14:45:04Z-
dc.date.available2020-04-02T14:45:04Z-
dc.date.issued2020en_US
dc.identifier.citationChiang Mai Journal of Science 47, 1 (January 2020), 175-180en_US
dc.identifier.issn0125-2526en_US
dc.identifier.urihttp://epg.science.cmu.ac.th/ejournal/dl.php?journal_id=10585en_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/67340-
dc.description.abstractAn efficient method for nucleophilic aromatic substitution of 2-chloroquinoline-3-carbaldehydes is described for the synthesis of 6/8-methyl-2-(piperidin-1-yl)quinoline-3-carbaldehydes. The protocol involves the effective use of phase transfer catalyst CTAB in combination with polyethyleneglycol-400 to obtain the desired products in less reaction time. The newly developed method is found superior to the previously reported methods due to easy work up and excellent yields.en_US
dc.language.isoEngen_US
dc.publisherScience Faculty of Chiang Mai Universityen_US
dc.subjectquinolineen_US
dc.subjectnucleophilic aromatic substitutionen_US
dc.subjectphase transfer catalysten_US
dc.subjectCTABen_US
dc.subjectpiperidineen_US
dc.titleSynthesis of 6/8-Methyl-2-(piperidin-1-yl)quinoline-3-carbaldehydes: A Facile CTAB Catalyzed Protocolen_US
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