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dc.contributor.authorLee, KJ-
dc.contributor.authorSong, DH-
dc.contributor.authorKim, DJ-
dc.contributor.authorPark, SW-
dc.date.accessioned2024-01-21T19:04:22Z-
dc.date.available2024-01-21T19:04:22Z-
dc.date.created2022-01-10-
dc.date.issued1997-01-
dc.identifier.issn0022-152X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/144146-
dc.description.abstractThe reaction of benzil 1-ureidoethylidene hydrazones 8 with a mixture of triphenylphosphine, carbon tetrachloride, and triethylamine provides a general route to 7H-imidazo[1,2-b][1,2,4]triazoles 18 via the thermal reaction of the expected keto azine carbodiimide intermediates 13, and the structure of 18 was confirmed by X-ray crystallographic analysis.-
dc.languageEnglish-
dc.publisherHeterocorporation-
dc.titleA new synthetic route to 7H-imidazo[1,2-b][1,2,4]triazoles-
dc.typeArticle-
dc.identifier.doi10.1002/jhet.5570340112-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJournal of Heterocyclic Chemistry, v.34, no.71, pp.71 - 76-
dc.citation.titleJournal of Heterocyclic Chemistry-
dc.citation.volume34-
dc.citation.number71-
dc.citation.startPage71-
dc.citation.endPage76-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1997WM42900012-
dc.identifier.scopusid2-s2.0-0030972894-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlus1,2,4-TRIAZOLE FUSED HETEROCYCLES-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlus4H-1,2,4-TRIAZOLO<1,5-C><1,3,5>OXADIAZINES-
dc.subject.keywordPlusREARRANGEMENT-
dc.subject.keywordPlusAZINES-
dc.subject.keywordAuthor7H-imidazo[1-
dc.subject.keywordAuthor2-b][1-
dc.subject.keywordAuthor2-
dc.subject.keywordAuthor4]triazoles-
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