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ortho-Naphthoquinone-catalyzed aerobic oxidation of amines to fused pyrimidin-4(3H)-ones: a convergent synthetic route to bouchardatine and sildenafil

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dc.contributor.authorKim, Kyeongha-
dc.contributor.authorKim, Hun Young-
dc.contributor.authorOh, Kyungsoo-
dc.date.accessioned2022-01-19T01:44:26Z-
dc.date.available2022-01-19T01:44:26Z-
dc.date.issued2020-08-
dc.identifier.issn2046-2069-
dc.identifier.issn2046-2069-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/53815-
dc.description.abstractA facile access to fused pyrimidin-4(3H)-one derivatives has been established by using the metal-freeortho-naphthoquinone-catalyzed aerobic cross-coupling reactions of amines. The utilization of two readily available amines allowed a direct coupling strategy to quinazolinone natural product, bouchardatine, as well as sildenafil (Viagra (TM)) in a highly convergent manner.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleortho-Naphthoquinone-catalyzed aerobic oxidation of amines to fused pyrimidin-4(3H)-ones: a convergent synthetic route to bouchardatine and sildenafil-
dc.typeArticle-
dc.identifier.doi10.1039/d0ra06820a-
dc.identifier.bibliographicCitationRSC ADVANCES, v.10, no.52, pp 31101 - 31105-
dc.description.isOpenAccessN-
dc.identifier.wosid000566579400009-
dc.identifier.scopusid2-s2.0-85091120409-
dc.citation.endPage31105-
dc.citation.number52-
dc.citation.startPage31101-
dc.citation.titleRSC ADVANCES-
dc.citation.volume10-
dc.type.docTypeArticle-
dc.publisher.location영국-
dc.subject.keywordPlusONE-POT SYNTHESIS-
dc.subject.keywordPlusO-AMINOBENZAMIDES-
dc.subject.keywordPlusCASCADE SYNTHESIS-
dc.subject.keywordPlusN-HETEROCYCLES-
dc.subject.keywordPlusDOMINO SYNTHESIS-
dc.subject.keywordPlusAQUEOUS AMMONIA-
dc.subject.keywordPlusBENZYL ALCOHOLS-
dc.subject.keywordPlusLUOTONIN-B-
dc.subject.keywordPlusQUINAZOLINONES-
dc.subject.keywordPlusQUINAZOLIN-4(3H)-ONES-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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