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dc.contributor.authorFukuyama, Takahideen_US
dc.contributor.authorSugimori, Taikien_US
dc.contributor.authorMaetani, Shinjien_US
dc.contributor.authorRyu, Ilhyongen_US
dc.date.accessioned2019-04-02T05:59:48Z-
dc.date.available2019-04-02T05:59:48Z-
dc.date.issued2018-11-07en_US
dc.identifier.issn1477-0520en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c8ob01453aen_US
dc.identifier.urihttp://hdl.handle.net/11536/148362-
dc.description.abstractAn efficient approach to the synthesis of perinaphthenones via the rhodium-catalyzed dehydrative annulation of 1-naphthoic acids with internal alkynes was developed. Norbornadiene can act as an acetylene equivalent to give unsubstituted perinaphthenones at the 2- and 3-positions via dehydrative annulation followed by a retro Diels-Alder reaction.en_US
dc.language.isoen_USen_US
dc.titleSynthesis of perinaphthenones through rhodium-catalyzed dehydrative annulation of 1-naphthoic acids with alkynesen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c8ob01453aen_US
dc.identifier.journalORGANIC & BIOMOLECULAR CHEMISTRYen_US
dc.citation.volume16en_US
dc.citation.spage7583en_US
dc.citation.epage7587en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000448344400008en_US
dc.citation.woscount0en_US
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