DSpace at KISTKIST Article2009

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dc.contributor.authorCho, Young Ae-
dc.contributor.authorKim, Dong-Su-
dc.contributor.authorAhn, Hong Ryul-
dc.contributor.authorCanturk, Belgin-
dc.contributor.authorMolander, Gary A.-
dc.contributor.authorHam, Jungyeob-
dc.date.accessioned2024-01-20T20:32:19Z-
dc.date.available2024-01-20T20:32:19Z-
dc.date.created2021-09-04-
dc.date.issued2009-10-01-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/132042-
dc.description.abstractPotassium azidoaryltrifluoroborates have been prepared from the corresponding haloaryltrifluoroborates in 73-98% yields. Also, we successfully cross-coupled the azido-functionalized organotrifluoroborates and carried out a one-pot sequential cross-coupling/1,3-dipolar cycloaddition and a one-pot cross-coupling/azide reduction process.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectCLICK CHEMISTRY-
dc.subjectAZIDES-
dc.subjectCYCLOADDITION-
dc.titlePreparation of Potassium Azidoaryltrifluoroborates and Their Cross-Coupling with Aryl Halides-
dc.typeArticle-
dc.identifier.doi10.1021/ol901669k-
dc.description.journalClass1-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.11, no.19, pp.4330 - 4333-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume11-
dc.citation.number19-
dc.citation.startPage4330-
dc.citation.endPage4333-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000269989100021-
dc.identifier.scopusid2-s2.0-70350153799-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusCLICK CHEMISTRY-
dc.subject.keywordPlusAZIDES-
dc.subject.keywordPlusCYCLOADDITION-
dc.subject.keywordAuthorOrganotrifluoroborate-
dc.subject.keywordAuthorhaloaryltrifluoroborate-
dc.subject.keywordAuthorAzidoaryltrifluoroborate-
dc.subject.keywordAuthorCross-Coupling-
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