A NOVEL METHOD OF ARYLATION OF
M Durandetti, S Sibille, JY Nédélec…
Index: Durandetti; Sibille; Nedelec; Perichon Synthetic Communications, 1994 , vol. 24, # 2 p. 145 - 151
Full Text: HTML
Citation Number: 0
Abstract
Abstract: Ot—Arylated ketones were obtained in moderate to good yields by onestep electroreductive coupling of Ct—chloroketones and arylhalides in DMF and in the presence of a Al-or Zn-sacrificial anode and a catalytic amount of a nickel complex. l-Aryl—Z— propanones are versatile intermediates for the synthesis of pharmaceuticals, agrochemicals, and fragrances. Two general approaches have been used to arylate ketones at the a- ...
Related Articles:
[Ackermann, Lutz; Mehta, Vaibhav P. Chemistry - A European Journal, 2012 , vol. 18, # 33 p. 10230 - 10233]
[Barcus, Robert L.; Wright, Bradford B.; Platz, Matthew S.; Scaiano, J. C. Tetrahedron Letters, 1983 , vol. 24, # 37 p. 3955 - 3958]
[Tamura, Yasumitsu; Choi, Hong Dae; Mizutani, Masako; Ueda, Yuko; Ishibashi, Hiroyuki Chemical and Pharmaceutical Bulletin, 1982 , vol. 30, # 10 p. 3574 - 3579]
[Barcus, R. L.; Hadel, L. M.; Johnston, L. J.; Platz, M. S.; Savino, T. G.; Scaiano, J. C. Journal of the American Chemical Society, 1986 , vol. 108, # 14 p. 3928 - 3937]
[Okabe, Kazuaki; Ohwada, Tomohiko; Ohta, Toshiharu; Shudo, Koichi Journal of Organic Chemistry, 1989 , vol. 54, # 4 p. 733 - 734]