REGIOSELECTIVE PHENYLSELENENYLATION AT THE 5-POSITION OF PYRIMIDINE NUCLEOSIDES MEDIATED BY MANGANESE(III) ACETATE

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dc.contributor.authorD. H. Leeko
dc.contributor.authorKim, Yong Haeko
dc.date.accessioned2013-02-28T01:58:18Z-
dc.date.available2013-02-28T01:58:18Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1995-
dc.identifier.citationSYNLETT, no.4, pp.349 - 350-
dc.identifier.issn0936-5214-
dc.identifier.urihttp://hdl.handle.net/10203/72170-
dc.description.abstract5-(Phenylseleno)pyrimidine nucleosides are obtained in high yields by the reaction of pyrimidine nucleosides with manganese (III) acetate and diphenyl diselenide in acetic acid. A selenium electrophile generated by the reaction of manganese(III) acetate with diphenyl diselenide appears to take an important role.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG-
dc.subjectURACILS-
dc.titleREGIOSELECTIVE PHENYLSELENENYLATION AT THE 5-POSITION OF PYRIMIDINE NUCLEOSIDES MEDIATED BY MANGANESE(III) ACETATE-
dc.typeArticle-
dc.identifier.wosidA1995QT20000021-
dc.type.rimsART-
dc.citation.issue4-
dc.citation.beginningpage349-
dc.citation.endingpage350-
dc.citation.publicationnameSYNLETT-
dc.contributor.nonIdAuthorD. H. Lee-
dc.type.journalArticleNote-
dc.subject.keywordPlusURACILS-
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