Iptycenes with an acridinone motif developed through [4+2] cycloaddition of tethered naphthalene and iminoquinone via a radical reaction

dc.citation.epage	6250	en_US
dc.citation.spage	6247	en_US
dc.citation.volume	53	en_US
dc.contributor.author	Raju, Selvam	en_US
dc.contributor.author	Annamalai, Pratheepkumar	en_US
dc.contributor.author	Chen, Pei-Ling	en_US
dc.contributor.author	Liu, Yi-Hung	en_US
dc.contributor.author	Chuang, Shih-Ching	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.date.accessioned	2018-08-21T05:54:07Z
dc.date.available	2018-08-21T05:54:07Z
dc.date.issued	2017-06-11	en_US
dc.description.abstract	A 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.identifier.doi	10.1039/c7cc03030d	en_US
dc.identifier.issn	1359-7345	en_US
dc.identifier.journal	CHEMICAL COMMUNICATIONS	en_US
dc.identifier.uri	http://dx.doi.org/10.1039/c7cc03030d	en_US
dc.identifier.uri	https://ir.lib.nycu.edu.tw/handle/11536/145597
dc.identifier.wosnumber	WOS:000402728600016	en_US
dc.language.iso	en_US	en_US
dc.title	Iptycenes with an acridinone motif developed through [4+2] cycloaddition of tethered naphthalene and iminoquinone via a radical reaction	en_US
dc.type	Article	en_US

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