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dc.contributor.authorHahn, HG-
dc.contributor.authorNam, KD-
dc.contributor.authorMah, H-
dc.date.accessioned2024-01-21T10:05:57Z-
dc.date.available2024-01-21T10:05:57Z-
dc.date.created2021-09-01-
dc.date.issued2002-09-01-
dc.identifier.issn0385-5414-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/139216-
dc.description.abstractA new synthesis of pyrrolo[2,1-b]thiazoles (5) is described. Hydrolysis of acetoxy djhydro-1,4-thiazine (2) prepared by Pummerer reaction of dihydro-1,4-thiazine sulfoxide gave the intermediate alpha-hydroxy sulfide (4). Dehydration of 4 gave pyrrolo[2,1-b]thiazoles (5). The reaction mechanism for the formation of 5 including the intermediate thiol (6) is discussed.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleUnexpected formation of pyrrolo[2,1-b]thiazoles by rearrangement of alpha-hydroxydihydro-1,4-thiazines-
dc.typeArticle-
dc.identifier.doi10.3987/COM-02-9540-
dc.description.journalClass1-
dc.identifier.bibliographicCitationHETEROCYCLES, v.57, no.9, pp.1697 - 1704-
dc.citation.titleHETEROCYCLES-
dc.citation.volume57-
dc.citation.number9-
dc.citation.startPage1697-
dc.citation.endPage1704-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000178032100012-
dc.identifier.scopusid2-s2.0-0036731736-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordAuthordihydro-1-
dc.subject.keywordAuthor4-thiazine-
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