Metal-free N-iodosuccinimide-catalyzed mild oxidative C–H bond amination of benzoxazoles
YS Wagh, DN Sawant, BM Bhanage
Index: Wagh, Yogesh S.; Sawant, Dinesh N.; Bhanage, Bhalchandra M. Tetrahedron Letters, 2012 , vol. 53, # 27 p. 3482 - 3485
Full Text: HTML
Citation Number: 17
Abstract
A facile, efficient, and mild protocol for the synthesis of aminobenzoxazoles has been developed using direct oxidative C–H bond amination of benzoxazoles with secondary or primary amines. The reaction was performed using catalytic amount of N-iodosuccinimide and aqueous hydrogen peroxide as a green oxidant and in the absence of transition metals. Reaction proceeds smoothly at ambient temperature and requires shorter reaction time to ...
Related Articles:
[Liu, Bifu; Yin, Meizhou; Gao, Hanling; Wu, Wanqing; Jiang, Huanfeng Journal of Organic Chemistry, 2013 , vol. 78, # 7 p. 3009 - 3020]
Iron-catalyzed direct amination of azoles using formamides or amines as nitrogen sources in air
[Wang, Jian; Hou, Ji-Ting; Wen, Jun; Zhang, Ji; Yu, Xiao-Qi Chemical Communications, 2011 , vol. 47, # 12 p. 3652 - 3654]