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Cited 7 time in webofscience Cited 7 time in scopus
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Pd-catalyzed oxa-[4+n] dipolar cycloaddition using 1,4-O/C dipole synthons for the synthesis of O-heterocycles

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dc.contributor.authorCho, Ho-Jun-
dc.contributor.authorKim, Ju Hyun-
dc.date.accessioned2023-12-27T01:00:22Z-
dc.date.available2023-12-27T01:00:22Z-
dc.date.issued2023-12-
dc.identifier.issn1477-0520-
dc.identifier.issn1477-0539-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/69000-
dc.description.abstractTransition metal-catalyzed dipolar cycloaddition is one of the most efficient and powerful synthetic strategies to produce diverse heterocycles. In particular, for the construction of oxygen-containing heterocycles, which are valuable structural motifs found in pharmaceuticals and natural compounds, transition metal-catalyzed oxa-dipolar cycloaddition using an oxygen-containing dipole has emerged as a promising method. In recent years, the 1,4-O/C dipole synthons 2-alkylidenetrimethylene carbonate and 2-hydroxymethylallyl carbonate have been developed and successfully applied to palladium-catalyzed oxa-[4 + n] dipolar cycloadditions with diverse dipolarophiles. In this review, we summarize recent advances in palladium-catalyzed oxa-[4 + n] dipolar cycloadditions using 1,4-O/C dipoles including asymmetric catalysis and divergent catalysis toward five- to nine-membered O-heterocycles.-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherRoyal Society of Chemistry-
dc.titlePd-catalyzed oxa-[4+n] dipolar cycloaddition using 1,4-O/C dipole synthons for the synthesis of O-heterocycles-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1039/d3ob01619f-
dc.identifier.scopusid2-s2.0-85178610503-
dc.identifier.wosid001109883800001-
dc.identifier.bibliographicCitationOrganic and Biomolecular Chemistry, v.21, no.48, pp 9507 - 9518-
dc.citation.titleOrganic and Biomolecular Chemistry-
dc.citation.volume21-
dc.citation.number48-
dc.citation.startPage9507-
dc.citation.endPage9518-
dc.type.docTypeReview-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusRING-CLOSURE REACTIONS-
dc.subject.keywordPlusASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlusPALLADIUM-
dc.subject.keywordPlusTRIMETHYLENEMETHANE-
dc.subject.keywordPlusMETHYLENETETRAHYDROFURANS-
dc.subject.keywordPlusANNULATIONS-
dc.subject.keywordPlusCYCLIZATION-
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