Direct C-H cross-coupling approach to heteroaryl coumarins

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dc.contributor.authorMin, Minsikko
dc.contributor.authorKim, Bomiko
dc.contributor.authorHong, Sungwooko
dc.date.accessioned2013-03-11T05:15:10Z-
dc.date.available2013-03-11T05:15:10Z-
dc.date.created2012-04-24-
dc.date.created2012-04-24-
dc.date.issued2012-02-
dc.identifier.citationORGANIC BIOMOLECULAR CHEMISTRY, v.10, no.13, pp.2692 - 2698-
dc.identifier.issn1477-0520-
dc.identifier.urihttp://hdl.handle.net/10203/98338-
dc.description.abstractA Pd-catalyzed direct cross-coupling of 3-bromocoumarins with heteroarenes provided an efficient route to synthesizing 3-heteroarylcoumarins. The reaction scope for the transformation was fairly broad, affording modest to good yields of various 3-heteroarylcoumarin scaffolds, which are privileged structures and prevalent motifs in many biologically active compounds and fluorophores.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectCATALYZED DIRECT ARYLATION-
dc.subjectONE-POT SYNTHESIS-
dc.subjectUNACTIVATED ARENES-
dc.subjectN-OXIDES-
dc.subjectFUNCTIONALIZATION-
dc.subjectDERIVATIVES-
dc.subjectINHIBITORS-
dc.subjectPHOTOCHEMISTRY-
dc.subjectHETEROCYCLES-
dc.subjectALKYNOATES-
dc.titleDirect C-H cross-coupling approach to heteroaryl coumarins-
dc.typeArticle-
dc.identifier.wosid000301234600029-
dc.identifier.scopusid2-s2.0-84863341440-
dc.type.rimsART-
dc.citation.volume10-
dc.citation.issue13-
dc.citation.beginningpage2692-
dc.citation.endingpage2698-
dc.citation.publicationnameORGANIC BIOMOLECULAR CHEMISTRY-
dc.identifier.doi10.1039/c2ob07137a-
dc.contributor.localauthorHong, Sungwoo-
dc.type.journalArticleArticle-
dc.subject.keywordPlusCATALYZED DIRECT ARYLATION-
dc.subject.keywordPlusONE-POT SYNTHESIS-
dc.subject.keywordPlusUNACTIVATED ARENES-
dc.subject.keywordPlusN-OXIDES-
dc.subject.keywordPlusFUNCTIONALIZATION-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusPHOTOCHEMISTRY-
dc.subject.keywordPlusHETEROCYCLES-
dc.subject.keywordPlusALKYNOATES-
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