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Transformations of 4-N-arylamino-4-(8-quinolinyl)-1-butenes and 3-aryl-2-(8-quinolinyl)4-thiazolidinones

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dc.contributor.authorMéndez, LYV
dc.contributor.authorKouznetsov, V
dc.contributor.authorPoveda, JC
dc.contributor.authorYolaçan, C
dc.contributor.authorÖcal, N
dc.contributor.authorAydogan, F
dc.date.accessioned2026-06-27T12:59:20Z
dc.date.issued2001
dc.description.abstractThe chemistry of 4-N-arylamino-4-(8-quinolinyl)-1-butenes 1-5 and 3-aryl-2-(8-quinolinyl)-4-thiazolidinones 15 has been studied. N-Furoylation, N-allylation, mediated-acid intramolecular cyclisation. amino-Claisen transposition and aldol reactions were used to prepare new C-8 substituted quinolines with biological potential.en
dc.identifier.endpage134
dc.identifier.issn0793-0283
dc.identifier.issue2
dc.identifier.startpage129
dc.identifier.urihttps://hdl.handle.net/20.500.14981/48621
dc.identifier.volume7
dc.identifier.wos000170072000005
dc.language.isoeng
dc.publisherFREUND PUBLISHING HOUSE LTD
dc.relation.ispartofHETEROCYCLIC COMMUNICATIONS
dc.subjectChemistry
dc.titleTransformations of 4-N-arylamino-4-(8-quinolinyl)-1-butenes and 3-aryl-2-(8-quinolinyl)4-thiazolidinones
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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