Thioethers as Directing Group for the Palladium??Catalyzed Direct Arylation of Arenes
J Yao, M Yu, Y Zhang
Index: Yao, Jinzhong; Yu, Ming; Zhang, Yuhong Advanced Synthesis and Catalysis, 2012 , vol. 354, # 17 p. 3205 - 3210
Full Text: HTML
Citation Number: 25
Abstract
Abstract Thioethers have proven to be efficient directing groups for the arylation of arenes under palladium catalysis. The thioether group can be readily removed or converted to other functional groups. Kinetic isotopic effect studies reveal that the C [BOND] H cleavage of arenes might be the turnover-limiting step.
Related Articles:
[Mouesca; Rius; Lamotte Journal of the American Chemical Society, 1993 , vol. 115, # 11 p. 4714 - 4731]
[Mouesca; Rius; Lamotte Journal of the American Chemical Society, 1993 , vol. 115, # 11 p. 4714 - 4731]
[Mouesca; Rius; Lamotte Journal of the American Chemical Society, 1993 , vol. 115, # 11 p. 4714 - 4731]
Micellar systems as supercages for reactions of geminate radical pairs. Magnetic effects
[Turro, Nicholas J.; Weed, Gregory C. Journal of the American Chemical Society, 1983 , vol. 105, # 7 p. 1861 - 1868]