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dc.contributor.author박혜영-
dc.date.accessioned2016-08-28T11:08:29Z-
dc.date.available2016-08-28T11:08:29Z-
dc.date.issued2005-
dc.identifier.issn0385-5414-
dc.identifier.otherOAK-12852-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/228917-
dc.description.abstract2-Aminothiazolo[5,4-b]pyridines and 2-aminobenzoxazoles havebeen synthesized from 2-hydroxy-3-thioureidopyridine and 2-hydroxy-3-thioureidobenzene respectively via acid catalyzed cyclization, which were prepared by the reaction of isothiocyanates with 2-hydroxy-3-aminopyridine or 2-aminophenol. The hydroxyl group of N-(2-hydroxy-5-phenyl)-N′-phenyl thiourea reacted as nucleophile to thioureido carbon to give 2-aminobenzoxazoles, whereas that of N-(2-hydroxypyridino)-N′-phenylthiourea was reacted as leaving group upon nuclephillic sulfur of thiourea group in the presence of trifluoroacetic acid or phosphoric acid. © 2005 The Japan Institute of Heterocyclic Chemistry.-
dc.languageEnglish-
dc.titleA facile synthesis of 2-aminothiazolo[5,4-b]pyridines and2-aminobanzoxazoles via cyclization of thioureas-
dc.typeArticle-
dc.relation.issue11-
dc.relation.volume65-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage2729-
dc.relation.lastpage2740-
dc.relation.journaltitleHeterocycles-
dc.identifier.doi10.3987/COM-05-10440-
dc.identifier.wosidWOS:000233325300015-
dc.identifier.scopusid2-s2.0-33744465063-
dc.author.googleYoon J.H.-
dc.author.googleSong H.-
dc.author.googleKim S.W.-
dc.author.googleHan G.-
dc.author.googleChoo H.-Y.P.-
dc.contributor.scopusid박혜영(34972649500;57200273796)-
dc.date.modifydate20230411110509-
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약학대학 > 약학과 > Journal papers
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