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

Selvam Raju, Pratheepkumar Annamalai, Pei Ling Chen, Yi Hung Liu, Shih-Ching Chuang*

*Corresponding author for this work

研究成果: Article同行評審

2 引文 斯高帕斯(Scopus)

摘要

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.

原文English
頁(從 - 到)6247-6250
頁數4
期刊Chemical Communications
53
發行號46
DOIs
出版狀態Published - 1 一月 2017

指紋 深入研究「Iptycenes with an acridinone motif developed through [4+2] cycloaddition of tethered naphthalene and iminoquinone: Via a radical reaction」主題。共同形成了獨特的指紋。

引用此