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dc.contributor.authorSong, HJ-
dc.contributor.authorKim, MY-
dc.contributor.authorKang, SB-
dc.contributor.authorChung, BY-
dc.contributor.authorKim, Y-
dc.date.accessioned2024-01-21T17:33:55Z-
dc.date.available2024-01-21T17:33:55Z-
dc.date.created2022-01-10-
dc.date.issued1998-01-01-
dc.identifier.issn0385-5414-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/143296-
dc.description.abstractSome indole-fused tri-and tetracyclic 4-oxo-pyridine-3-carboxylic acids, quinolone-type derivatives, (3), (4), and (5) have been prepared. The synthesis is characterized by the construction of the pyridone ring through the intrarmolecular nucleophilic displacement cyclization at the 2-position of 3-substituted 1-methoxyindole accompanied with demethoxylation.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectANTIBACTERIAL AGENTS-
dc.subjectINVITRO-
dc.subjectQUINOLONES-
dc.titleSynthesis of indole-fused 4-pyridone-3-carboxylic acids-
dc.typeArticle-
dc.description.journalClass1-
dc.identifier.bibliographicCitationHETEROCYCLES, v.48, no.1, pp.103 - 112-
dc.citation.titleHETEROCYCLES-
dc.citation.volume48-
dc.citation.number1-
dc.citation.startPage103-
dc.citation.endPage112-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000071802800014-
dc.identifier.scopusid2-s2.0-0006066950-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusANTIBACTERIAL AGENTS-
dc.subject.keywordPlusINVITRO-
dc.subject.keywordPlusQUINOLONES-
dc.subject.keywordAuthorquinolones-
dc.subject.keywordAuthorantibacterial drugs-
dc.subject.keywordAuthor4-pyridone-3-carboxylic acids-
dc.subject.keywordAuthorintramolecular nucleophilic displacement-
dc.subject.keywordAuthorcyclization-
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