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dc.contributor.authorKim, Han Byeol-
dc.contributor.authorJeong, Hee Jin-
dc.contributor.authorCheong Jaeeun-
dc.contributor.authorLee, Jae Kyun-
dc.contributor.authorLee, Duck-Hyung-
dc.contributor.authorHan, Seojung-
dc.date.accessioned2024-01-12T06:35:21Z-
dc.date.available2024-01-12T06:35:21Z-
dc.date.created2023-05-30-
dc.date.issued2023-07-
dc.identifier.issn0022-3263-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/79890-
dc.description.abstractA mild,efficient, and transition-metal-free three-component couplingreaction involving arynes, phosphites, and aldehydes was establishedto afford 3-mono-substituted benzoxaphosphole 1-oxides. A range of3-mono-substituted benzoxaphosphole 1-oxides was obtained from botharyl- and aliphatic-substituted aldehydes in moderate to good yields.Moreover, the synthetic utility of the reaction was demonstrated bya Gram-scale reaction and the transformation of the products intovarious P-containing bicycles.-
dc.languageEnglish-
dc.publisherAmerican Chemical Society-
dc.titleThree-Component Coupling Reactions Involving Arynes, Phosphites, and Aldehydes toward 3-Mono-Substituted Benzoxaphosphole 1-Oxides-
dc.typeArticle-
dc.identifier.doi10.1021/acs.joc.3c00438-
dc.description.journalClass1-
dc.identifier.bibliographicCitationThe Journal of Organic Chemistry, v.88, no.13, pp.8465 - 8479-
dc.citation.titleThe Journal of Organic Chemistry-
dc.citation.volume88-
dc.citation.number13-
dc.citation.startPage8465-
dc.citation.endPage8479-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid001011705300001-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
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