NOVEL REGIOSELECTIVE FUNCTIONALIZATION AT THE 5-POSITION OF URACIL DERIVATIVES

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dc.contributor.authorD. H. Leeko
dc.contributor.authorS. G. Yangko
dc.contributor.authorKim, Yong Haeko
dc.date.accessioned2013-02-27T12:19:10Z-
dc.date.available2013-02-27T12:19:10Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1995-
dc.identifier.citationTETRAHEDRON LETTERS, v.36, no.28, pp.5027 - 5030-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/68530-
dc.description.abstractVarious pyrimidine bases reacted with diethyl malonate in the presence of manganese(III) acetate or Ce(NH4)(2)(NO3)(6) to give 5-(bis(ethoxycarbonyl)acetoxymethyl) pyrimidine nucleosides or 5-(bis(ethoxycarbonyl)methoxymethyl)pyrimidine nucleosides in good yields, respectively.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectNUCLEOSIDES-
dc.subjectANALOGS-
dc.titleNOVEL REGIOSELECTIVE FUNCTIONALIZATION AT THE 5-POSITION OF URACIL DERIVATIVES-
dc.typeArticle-
dc.identifier.wosidA1995RJ58300029-
dc.identifier.scopusid2-s2.0-0029078932-
dc.type.rimsART-
dc.citation.volume36-
dc.citation.issue28-
dc.citation.beginningpage5027-
dc.citation.endingpage5030-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.identifier.doi10.1016/0040-4039(95)00913-W-
dc.contributor.nonIdAuthorD. H. Lee-
dc.contributor.nonIdAuthorS. G. Yang-
dc.type.journalArticleArticle-
dc.subject.keywordPlusNUCLEOSIDES-
dc.subject.keywordPlusANALOGS-
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