Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2019
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dc.contributor.authorG, Selvi-
dc.contributor.authorS P, Rajendran-
dc.date.accessioned2020-10-05T09:32:57Z-
dc.date.available2020-10-05T09:32:57Z-
dc.date.issued2010-05-15-
dc.identifier.urihttps://doi.org/10.1515/HC.2009.15.5.349-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/2019-
dc.description.abstract2-phenyl-4-chloro-3-formyl quinoline 2 was obtained by the reaction of 1 with POCls/DMF in CTAB medium. The newly synthesized aldehyde was then converted to acrylic ester 4 via its acid 3 which was then brominated and chlorinated to get the trihalocompound 7. The trihalocompound thus obtained was treated with thiourea to get the titled compound 8.en_US
dc.language.isoenen_US
dc.publisherHeterocyclic Communicationsen_US
dc.titleCONVENIENT SYNTHESIS OF 2-PHENYL-4-CHLORO-3-FORMYLQUINOLINE AND ITS UTILITY FOR THE SYNTHESIS OF THIENO[3,2-C]-4-PHENYLQUINOLINE-2-CARBOXYLIC ACIDen_US
dc.typeArticleen_US
Appears in Collections:International Journals



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