DC Field | Value | Language |
---|---|---|
dc.contributor.author | k.r.roh | ko |
dc.contributor.author | h.k.chang | ko |
dc.contributor.author | Kim, Yong Hae | ko |
dc.date.accessioned | 2013-02-27T19:25:21Z | - |
dc.date.available | 2013-02-27T19:25:21Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 1998 | - |
dc.identifier.citation | HETEROCYCLES, v.48, no.3, pp.437 - 441 | - |
dc.identifier.issn | 0385-5414 | - |
dc.identifier.uri | http://hdl.handle.net/10203/70374 | - |
dc.description.abstract | A 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.language | English | - |
dc.publisher | Pergamon-Elsevier Science Ltd | - |
dc.subject | PROTECTING GROUP | - |
dc.subject | VINYL HALIDES | - |
dc.subject | C-5 | - |
dc.subject | IONS | - |
dc.subject | URIDINES | - |
dc.subject | ROUTE | - |
dc.title | Efficient Phenylsulfenylation and Phenylselenenylation at the 5-Position of Uracil Nucleosides with Disulfide and Diselenide Mediated by [Bis(Trifluoroacetoxy)iodo]Benzene | - |
dc.type | Article | - |
dc.identifier.wosid | 000073111100004 | - |
dc.identifier.scopusid | 2-s2.0-0041488356 | - |
dc.type.rims | ART | - |
dc.citation.volume | 48 | - |
dc.citation.issue | 3 | - |
dc.citation.beginningpage | 437 | - |
dc.citation.endingpage | 441 | - |
dc.citation.publicationname | HETEROCYCLES | - |
dc.contributor.nonIdAuthor | k.r.roh | - |
dc.contributor.nonIdAuthor | h.k.chang | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordPlus | PROTECTING GROUP | - |
dc.subject.keywordPlus | VINYL HALIDES | - |
dc.subject.keywordPlus | C-5 | - |
dc.subject.keywordPlus | IONS | - |
dc.subject.keywordPlus | URIDINES | - |
dc.subject.keywordPlus | ROUTE | - |
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