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Cited 34 time in webofscience Cited 36 time in scopus
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dc.contributor.authorBork, JT-
dc.contributor.authorLee, JW-
dc.contributor.authorChang, Young-Tae-
dc.date.accessioned2018-06-15T05:11:15Z-
dc.date.available2018-06-15T05:11:15Z-
dc.date.created2017-09-08-
dc.date.issued2003-08-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/50184-
dc.description.abstractTo introduce the biaryl structure as a triazine functionality, we have developed a new synthetic route via the Suzuki cross-coupling reaction of resin-bound chlorotriazines. The Suzuki cross-coupling reaction was achieved using various arylboronic acids, Pd(PPh3)(4), Cs2CO3, and dioxane. With the integration of this chemistry and our previous orthogonal methodology, the triazine library is greatly expanded to a biaryl scaffold. (C) 2003 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfTETRAHEDRON LETTERS-
dc.subjectBULKY ARYLBORONIC ACID-
dc.subjectSOLID-PHASE SYNTHESIS-
dc.subjectARYL CHLORIDES-
dc.subjectHETEROARYL CHLORIDES-
dc.subject6-HALOPURINES-
dc.subjectHALOPYRIDINES-
dc.subjectCONVENIENT-
dc.subjectTRIAZINES-
dc.subjectARYLATION-
dc.subjectDISCOVERY-
dc.titlePalladium-catalyzed cross-coupling reaction of resin-bound chlorotriazines-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4039(03)01451-5-
dc.type.rimsART-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.44, no.32, pp.6141 - 6144-
dc.identifier.wosid000184367200043-
dc.date.tcdate2019-02-01-
dc.citation.endPage6144-
dc.citation.number32-
dc.citation.startPage6141-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume44-
dc.contributor.affiliatedAuthorChang, Young-Tae-
dc.identifier.scopusid2-s2.0-0038644076-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc34-
dc.type.docTypeArticle-
dc.subject.keywordPlusBULKY ARYLBORONIC ACID-
dc.subject.keywordPlusSOLID-PHASE SYNTHESIS-
dc.subject.keywordPlusARYL CHLORIDES-
dc.subject.keywordPlusHETEROARYL CHLORIDES-
dc.subject.keywordPlus6-HALOPURINES-
dc.subject.keywordPlusHALOPYRIDINES-
dc.subject.keywordPlusCONVENIENT-
dc.subject.keywordPlusTRIAZINES-
dc.subject.keywordPlusARYLATION-
dc.subject.keywordPlusDISCOVERY-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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