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dc.contributor.authorJeong, Hee Jin-
dc.contributor.authorKim, Ji Ho-
dc.contributor.authorLee, Jae Kyun-
dc.contributor.authorYoon, Hyo Jae-
dc.contributor.authorChoi, Junwon-
dc.contributor.authorHan, Seo-Jung-
dc.date.accessioned2024-01-12T03:32:10Z-
dc.date.available2024-01-12T03:32:10Z-
dc.date.created2022-03-25-
dc.date.issued2022-03-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/76779-
dc.description.abstractAn efficient and transition-metal-free three-component reaction with benzynes formed in situ from 2-(trimethylsilyl)aryl triflate, phosphites, and ketones was developed for the synthesis of benzox-aphosphole 1-oxides. An array of benzoxaphosphole 1-oxides were prepared from both activated and non-activated ketones in moderate to good yields with a broad functional group tolerance. This reaction is useful for preparing organophosphorus compounds encountered in natural products and materials.-
dc.languageEnglish-
dc.publisherAmerican Chemical Society-
dc.titleSynthesis of Benzoxaphosphole 1-Oxide Heterocycles via a Three-Component Coupling Reaction Involving Arynes, Phosphites, and Ketones-
dc.typeArticle-
dc.identifier.doi10.1021/acs.orglett.2c00515-
dc.description.journalClass1-
dc.identifier.bibliographicCitationOrganic Letters, v.24, no.11, pp.2192 - 2196-
dc.citation.titleOrganic Letters-
dc.citation.volume24-
dc.citation.number11-
dc.citation.startPage2192-
dc.citation.endPage2196-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000777746600022-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
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KIST Article > 2022
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