Formation of bi-aryls via a domino palladium catalysis
J Krishna, AGK Reddy, G Satyanarayana
Index: Krishna; Reddy, A. Gopi Krishna; Satyanarayana Tetrahedron Letters, 2014 , vol. 55, # 4 p. 861 - 864
Full Text: HTML
Citation Number: 11
Abstract
Abstract Synthesis of bi-aryls via a domino Pd-catalyzed reaction of 1-(2-bromophenyl)-2- methylpropan-1-ones/(2-bromophenyl)(cyclohexyl) methanones is presented. The mechanism of the reaction is believed to proceed through a five membered palladacycle that combines with a second molecule of halo-arene to yield the bi-aryls. This method is quite successful to deliver highly sterically crowded bi-aryls with dense functionalities on the ...
Related Articles:
Fe-Catalyzed Regiodivergent [1, 2]-Shift of α-Aryl Aldehydes
[Gutierrez-Bonet, Alvaro; Flores-Gaspar, Areli; Martin, Ruben Journal of the American Chemical Society, 2013 , vol. 135, # 34 p. 12576 - 12579]
[Korn, Tobias J.; Schade, Matthias A.; Cheemala, Murthy N.; Wirth, Stefan; Guevara, Simon A.; Cahiez, Gerard; Knochel, Paul Synthesis, 2006 , # 21 p. 3547 - 3574]
Fe-Catalyzed Regiodivergent [1, 2]-Shift of α-Aryl Aldehydes
[Gutierrez-Bonet, Alvaro; Flores-Gaspar, Areli; Martin, Ruben Journal of the American Chemical Society, 2013 , vol. 135, # 34 p. 12576 - 12579]
Fe-Catalyzed Regiodivergent [1, 2]-Shift of α-Aryl Aldehydes
[Gutierrez-Bonet, Alvaro; Flores-Gaspar, Areli; Martin, Ruben Journal of the American Chemical Society, 2013 , vol. 135, # 34 p. 12576 - 12579]