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dc.contributor.authorShin, Donghwa-
dc.contributor.authorKim, Soomin-
dc.contributor.authorLee, Duck-Hyung-
dc.contributor.authorHan, Seo-Jung-
dc.date.accessioned2024-06-13T02:00:17Z-
dc.date.available2024-06-13T02:00:17Z-
dc.date.created2024-06-13-
dc.date.issued2024-06-
dc.identifier.issn0022-3263-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/150059-
dc.description.abstractMild, metal-free, and operationally simple three-component coupling reactions involving arynes, phosphites, and acrylates have been achieved. The reaction proceeded well with alpha- or beta-substituted acrylates. Additionally, various functional groups were tolerated under these reaction conditions, resulting in diverse ortho-3-propanoate-substituted aryl phosphonates. Moreover, the reaction can be used to synthesize a range of organophosphorus compounds present in natural products, materials, and biologically active compounds.-
dc.languageEnglish-
dc.publisherAmerican Chemical Society-
dc.titleSynthetic Strategies toward Ortho-3-propanoate Substituted Aryl Phosphonates by Three-Component Coupling Reactions of Arynes, Phosphites, and Acrylates-
dc.typeArticle-
dc.identifier.doi10.1021/acs.joc.4c00672-
dc.description.journalClass1-
dc.identifier.bibliographicCitationThe Journal of Organic Chemistry, v.89, no.11, pp.8035 - 8040-
dc.citation.titleThe Journal of Organic Chemistry-
dc.citation.volume89-
dc.citation.number11-
dc.citation.startPage8035-
dc.citation.endPage8040-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid001234402900001-
dc.identifier.scopusid2-s2.0-85194484457-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusINHIBITOR-
dc.subject.keywordPlusALKENES-
dc.subject.keywordPlusP-ARYLATION-
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