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dc.contributor.authorHam, Young Jin-
dc.contributor.authorLee, Duck-Hyung-
dc.contributor.authorChoi, Hwan Geun-
dc.contributor.authorHah, Jung-Mi-
dc.contributor.authorSim, Taebo-
dc.date.accessioned2024-01-20T18:33:37Z-
dc.date.available2024-01-20T18:33:37Z-
dc.date.created2021-09-04-
dc.date.issued2010-09-01-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/131118-
dc.description.abstractA facile one-step transformation of methylsulfanyl and arylsulfanyl groups on pyrimidine ring system into the corresponding chloride group was achieved using sulfuryl chloride in acetonitrile/dichloromethane. (C) 2010 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectCROSS-COUPLING REACTIONS-
dc.subjectPURINE-
dc.subjectANTAGONISTS-
dc.titleThe efficient one-step chlorination of methylsulfanyl group on pyrimidine ring system with sulfuryl chloride-
dc.typeArticle-
dc.identifier.doi10.1016/j.tetlet.2010.06.056-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.51, no.35, pp.4609 - 4611-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume51-
dc.citation.number35-
dc.citation.startPage4609-
dc.citation.endPage4611-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000280953100005-
dc.identifier.scopusid2-s2.0-77955653370-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusCROSS-COUPLING REACTIONS-
dc.subject.keywordPlusPURINE-
dc.subject.keywordPlusANTAGONISTS-
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