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Please use this identifier to cite or link to this item: https://hdl.handle.net/10321/3008
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dc.contributor.authorPitchai, P.en_US
dc.contributor.authorNepolraj, A.en_US
dc.contributor.authorSathiyaseelan, M.en_US
dc.contributor.authorGengan, Robert Moonsamyen_US
dc.date.accessioned2018-06-04T06:39:37Z-
dc.date.available2018-06-04T06:39:37Z-
dc.date.issued2016-
dc.identifier.citationPitchai, P. et al. 2016. 4-Dihydroxy-3-(indol-2-)-yl-quinoline via substantial methodology-fisher indole synthesis. Heterocyclic Letters. 6(1): 11-14.en_US
dc.identifier.issn2231–3087 (print)-
dc.identifier.issn2230-9632 (online)-
dc.identifier.urihttp://hdl.handle.net/10321/3008-
dc.description.abstractFisher indole methodology, a simple application was used to generate indole as a substitution on the quinoline ring. Conventional heating and microwave irradiation was compared. The ease of work up procedure, reduced time and moreover the high yield is exceptional however microwave irradiation presented more advantages.en_US
dc.format.extent4 pen_US
dc.language.isoenen_US
dc.publisherHeterocyclic Lettersen_US
dc.relation.ispartofHeterocyclic lettersen_US
dc.subjectIndoleen_US
dc.subjectQuinolineen_US
dc.subjectFisher-indole methoden_US
dc.subject3-acyl-2en_US
dc.subject4-dihydroxyquinolineen_US
dc.title4-Dihydroxy-3-(indol-2-)-yl-quinoline via substantial methodology-fisher indole synthesisen_US
dc.typeArticleen_US
dc.publisher.urihttp://www.heteroletters.org/issue16/PDF/Paper-1.pdfen_US
dc.dut-rims.pubnumDUT-005855en_US
item.grantfulltextopen-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.openairetypeArticle-
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