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dc.contributor.authorRaju, Selvamen_US
dc.contributor.authorAnnamalai, Pratheepkumaren_US
dc.contributor.authorChen, Pei-Lingen_US
dc.contributor.authorLiu, Yi-Hungen_US
dc.contributor.authorChuang, Shih-Chingen_US
dc.date.accessioned2018-08-21T05:54:07Z-
dc.date.available2018-08-21T05:54:07Z-
dc.date.issued2017-06-11en_US
dc.identifier.issn1359-7345en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c7cc03030den_US
dc.identifier.urihttp://hdl.handle.net/11536/145597-
dc.description.abstractA new class of iptycenes was developed by combining 2-(naphthalen-1-yl) anilines and p-benzoquinones through copper( II)-mediated radical cyclisation. This unusual cyclisation reaction resulted in the robust and efficient syntheses of iptycenes with an acridinone motif. These iptycenes can be further transformed into planar acridinone heterocyclics through the Diels-Alder reaction.en_US
dc.language.isoen_USen_US
dc.titleIptycenes with an acridinone motif developed through [4+2] cycloaddition of tethered naphthalene and iminoquinone via a radical reactionen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c7cc03030den_US
dc.identifier.journalCHEMICAL COMMUNICATIONSen_US
dc.citation.volume53en_US
dc.citation.spage6247en_US
dc.citation.epage6250en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000402728600016en_US
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