Efficient Phenylsulfenylation and Phenylselenenylation at the 5-Position of Uracil Nucleosides with Disulfide and Diselenide Mediated by [Bis(Trifluoroacetoxy)iodo]Benzene

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dc.contributor.authork.r.rohko
dc.contributor.authorh.k.changko
dc.contributor.authorKim, Yong Haeko
dc.date.accessioned2013-02-27T19:25:21Z-
dc.date.available2013-02-27T19:25:21Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1998-
dc.identifier.citationHETEROCYCLES, v.48, no.3, pp.437 - 441-
dc.identifier.issn0385-5414-
dc.identifier.urihttp://hdl.handle.net/10203/70374-
dc.description.abstractA series of uracil nucleosides reacted with diphenyl disulfide or diphenyl diselenide in the presence of hypervalent iodine reagent, [bis(trifluoro-acetoxy)iodo]benzene, in acetonitrile to give the corresponding C-5 phenylsulfenylated or phenylselenenylated products respectively in excellent yields.-
dc.languageEnglish-
dc.publisherPergamon-Elsevier Science Ltd-
dc.subjectPROTECTING GROUP-
dc.subjectVINYL HALIDES-
dc.subjectC-5-
dc.subjectIONS-
dc.subjectURIDINES-
dc.subjectROUTE-
dc.titleEfficient Phenylsulfenylation and Phenylselenenylation at the 5-Position of Uracil Nucleosides with Disulfide and Diselenide Mediated by [Bis(Trifluoroacetoxy)iodo]Benzene-
dc.typeArticle-
dc.identifier.wosid000073111100004-
dc.identifier.scopusid2-s2.0-0041488356-
dc.type.rimsART-
dc.citation.volume48-
dc.citation.issue3-
dc.citation.beginningpage437-
dc.citation.endingpage441-
dc.citation.publicationnameHETEROCYCLES-
dc.contributor.nonIdAuthork.r.roh-
dc.contributor.nonIdAuthorh.k.chang-
dc.type.journalArticleArticle-
dc.subject.keywordPlusPROTECTING GROUP-
dc.subject.keywordPlusVINYL HALIDES-
dc.subject.keywordPlusC-5-
dc.subject.keywordPlusIONS-
dc.subject.keywordPlusURIDINES-
dc.subject.keywordPlusROUTE-
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