A new method for the catalytic aldol reaction to ketones
…, Y Suto, M Kanai, M Shibasaki
Index: Oisaki, Kounosuke; Suto, Yutaka; Kanai, Motomu; Shibasaki, Masakatsu Journal of the American Chemical Society, 2003 , vol. 125, # 19 p. 5644 - 5645
Full Text: HTML
Citation Number: 108
Abstract
A new method for the catalytic aldol reaction to ketones, using CuF⊙ 3PPh3⊙ 2EtOH complex as the catalyst and (EtO) 3SiF as the additive, is described. The reaction can be applied to a wide range of ketones and trimethylsilyl enolates. On the basis of mechanistic studies, a working hypothesis for the catalytic cycle is proposed, in which the dynamic ligand exchange mediated by copper silicates produces the active copper enolate. Moreover, the ...
Related Articles:
High-intensity ultrasound-promoted Reformatsky reactions
[Ross, Nathan A.; Bartsch, Richard A. Journal of Organic Chemistry, 2003 , vol. 68, # 2 p. 360 - 366]
Reformatsky reaction of?-chloroesters with carbonyl compounds with commercially available zinc
[Chavan, Subhash P.; Shivasankar; Sivappa Journal of Chemical Research, 2004 , # 6 p. 406 - 407]