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dc.contributor.authorLee, Tai-Huaen_US
dc.contributor.authorJayakumar, Jayachandranen_US
dc.contributor.authorCheng, Chien-Hongen_US
dc.contributor.authorChuang, Shih-Chingen_US
dc.date.accessioned2014-12-08T15:33:17Z-
dc.date.available2014-12-08T15:33:17Z-
dc.date.issued2013en_US
dc.identifier.issn1359-7345en_US
dc.identifier.urihttp://hdl.handle.net/11536/23171-
dc.identifier.urihttp://dx.doi.org/10.1039/c3cc47197gen_US
dc.description.abstractPalladium-catalyzed oxidative carbonylation of 2-arylphenols through C-H bond activation and C-C and C-O bond formation under acid-base free and mild conditions has been developed. The reaction tolerates a variety of substrates and provides biologically important benzopyranone derivatives in up to 87% isolated yield.en_US
dc.language.isoen_USen_US
dc.titleOne pot synthesis of bioactive benzopyranones through palladium-catalyzed C-H activation and CO insertion into 2-arylphenolsen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c3cc47197gen_US
dc.identifier.journalCHEMICAL COMMUNICATIONSen_US
dc.citation.volume49en_US
dc.citation.issue100en_US
dc.citation.spage11797en_US
dc.citation.epage11799en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000327500500025-
dc.citation.woscount10-
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