Palladium-catalyzed phenyl-selenylation with n-Bu 3 SnSePh in one-pot two-step reactions
M Bonaterra, SE Martín, RA Rossi
Index: Bonaterra, Mariana; Martin, Sandra E.; Rossi, Roberto A. Tetrahedron Letters, 2006 , vol. 47, # 21 p. 3511 - 3515
Full Text: HTML
Citation Number: 39
Abstract
We have studied the Pd-catalyzed cross-coupling reaction of a stannane derived from selenium n-Bu3SnSePh (1) with aryl and perfluoroalkyl iodides. Herein a very efficient one- pot two-step selenylation reaction to form a C–Se bond is reported. Ph2Se2 reacts with Na metal in liquid ammonia yielding PhSe− ions. To this solution n-Bu3SnCl was added to afford 1, which was introduced in the palladium-catalyzed coupling reaction without ...
Related Articles:
[Zheng, Bo; Gong, Ying; Xu, Hua-Jian Tetrahedron, 2013 , vol. 69, # 26 p. 5342 - 5347]
[Kundu, Debasish; Ahammed, Sabir; Ranu, Brindaban C. Organic Letters, 2014 , vol. 16, # 6 p. 1814 - 1817]
[Beletskaya; Sigeev; Peregudov; Petrovskii Russian Journal of Organic Chemistry, 2001 , vol. 37, # 10 p. 1463 - 1475]
[Li, Yaming; Wang, Huifeng; Li, Xiaoying; Chen, Tao; Zhao, Defeng Tetrahedron, 2010 , vol. 66, # 45 p. 8583 - 8586]
[Bridges, Alexander J.; Fischer, John W. Journal of Organic Chemistry, 1984 , vol. 49, # 16 p. 2954 - 2961]