Facile One??Pot Palladium??Catalyzed Sequential Coupling to Diarylmethanes by Using Aryl Methyl Ketones as the Methylene Donors
X Wang, LH Liu, JH Shi, J Peng, HY Tu…
Index: Wang, Xing; Liu, Lian-Hua; Shi, Jin-Hua; Peng, Ji; Tu, Hai-Yang; Zhang, Ai-Dong European Journal of Organic Chemistry, 2013 , # 30 p. 6870 - 6877
Full Text: HTML
Citation Number: 2
Abstract
Abstract A novel palladium-catalyzed coupling reaction of an aryl methyl ketone with two molecules of an aryl halide to yield symmetric diarylmethanes is described. In the facile one- pot reaction, the aryl methyl ketone acts as a formal methylene donor. The experimental facts, including TLC monitoring, speculated intermediates as the raw materials, analysis of the cesium benzoate coproduct by ex situ IR spectroscopy, and the cross-coupling ...
Related Articles:
[Surya Prakash; Do, Clement; Mathew, Thomas; Olah, George A. Catalysis Letters, 2011 , vol. 141, # 4 p. 507 - 511]
[Kale; Singh Journal of Molecular Catalysis A: Chemical, 2002 , vol. 184, # 1-2 p. 399 - 411]
[Grummitt; Jenkins Journal of the American Chemical Society, 1946 , vol. 68, p. 914]
[Das, Suven; Froehlich, Roland; Pramanik, Animesh Journal of Chemical Research, 2006 , # 2 p. 84 - 86]
[Halpern, Marc; Lysenko, Zenon Journal of Organic Chemistry, 1989 , vol. 54, # 5 p. 1201 - 1203]