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dc.contributor.authorRoh, YH-
dc.contributor.authorBae, JW-
dc.contributor.authorNam, GS-
dc.contributor.authorKim, JH-
dc.contributor.authorKim, SH-
dc.contributor.authorYoon, CM-
dc.date.accessioned2024-01-21T14:38:00Z-
dc.date.available2024-01-21T14:38:00Z-
dc.date.created2021-09-04-
dc.date.issued2000-01-
dc.identifier.issn0039-7911-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/141711-
dc.description.abstractThe reaction of 6-[1-Aza-2-(dimethylamino)prop-1-enyl]-5-iodo-1,3-dimethyluracil (3) with various olefins in the presence of a catalytic amount of Pd(OAc)(2) and 1.5 equiv. of K2CO3 in DMF at 120 degrees C gave the pyrido[2,3-d]pyrimidine derivatives (5a-b and 7a-d) in moderate to high yield.-
dc.languageEnglish-
dc.publisherTAYLOR & FRANCIS INC-
dc.subjectQUINAZOLINES-
dc.subjectURACILS-
dc.titlePalladium-catalyzed coupling reaction of iodouracil having acetamidine moiety with olefins-
dc.typeArticle-
dc.identifier.doi10.1080/00397910008087296-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSYNTHETIC COMMUNICATIONS, v.30, no.1, pp.81 - 86-
dc.citation.titleSYNTHETIC COMMUNICATIONS-
dc.citation.volume30-
dc.citation.number1-
dc.citation.startPage81-
dc.citation.endPage86-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000085358900012-
dc.identifier.scopusid2-s2.0-0033973637-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusQUINAZOLINES-
dc.subject.keywordPlusURACILS-
dc.subject.keywordAuthorpalladium-catalyzed-
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