1456728-72-5Relevant academic research and scientific papers
Palladium-catalyzed regio-selective oxidative C-H bond acylation of azoxybenzenes with alcohols
Hou, Lekai,Chen, Xiangxiang,Li, Shuang,Cai, Suxian,Zhao, Yanxia,Sun, Meng,Yang, Xiao-Juan
supporting information, p. 4160 - 4164 (2015/04/14)
A palladium-catalyzed regio-selective acylation of C-H bonds of azoxybenzenes with alcohols was developed using tert-butyl hydroperoxide (TBHP) as an oxidant. Alcohol derivatives can act as effective acyl precursors in situ, which are less toxic, inexpensive, stable, and commercially available. These transformations proceeded smoothly and could tolerate a variety of functional groups. This journal is
Palladium-catalyzed regioselective ortho-acylation of azoxybenzenes with aldehyde derivatives
Sun, Meng,Hou, Le-Kai,Chen, Xiang-Xiang,Yang, Xiao-Juan,Sun, Wei,Zang, Yu-Shi
supporting information, p. 3789 - 3793 (2015/02/19)
An efficient strategy for the regioselective ortho-acylation of azoxybenzenes with various aldehydes in the presence of palladium catalysts has been developed and furnishes good to excellent yields. The reaction proceeds smoothly and can tolerate a variety of functional groups.
Unprecedented ortho-acylation of azoxybenzenes with α-oxocarboxylic acids by Pd-catalyzed C-H activation and decarboxylation
Li, Hongji,Li, Pinhua,Zhao, Qiong,Wang, Lei
supporting information, p. 9170 - 9172 (2013/09/24)
A palladium-catalyzed ortho-acylation reaction of azoxybenzenes with α-oxocarboxylic acids was developed in the presence of K2S 2O8. The established methodology provides a direct approach to obtain acylated azoxybenzenes in good yields.
