1597444-14-8Relevant articles and documents
Cross-Dehydrogenative-Coupling of Alkoxybenzenes with Toluenes: Copper(II) Halide Mediated Tandem Halo/Benzylation of Arenes
Storr, Thomas E.,Teskey, Christopher J.,Greaney, Michael F.
supporting information, p. 18169 - 18178 (2016/12/16)
A cross-dehydrogenative-coupling of alkoxybenzenes and toluenes with concomitant halogenation is reported. Conditions employed were the use of stoichiometric copper halide salts and dialkylperoxides to afford a range of bromoalkoxydi- and triarylmethanes. Preliminary mechanistic studies suggest that the in situ production of haloarenes (or dihaloarenes) followed by a copper-mediated coupling of a benzylic radical is operational.
TfOH catalyzed synthesis of 9-arylfluorenes via tandem reaction under warm and efficient conditions
Li, Qingcui,Xu, Wengang,Hu, Jiaxing,Chen, Xiaoqing,Zhang, Fanglin,Zheng, Hua
, p. 27722 - 27725 (2014/07/21)
A tandem ring-closing reaction was developed for the synthesis of 9-arylfluorenes and their derivatives. The reaction is metal-free, straightforward and efficient under warm conditions. More than 99% yield is obtained. This journal is the Partner Organisations 2014.