THE DIPHENYLBORYL HEXACHLOROANTIMONATE PROMOTED FRIEDEL–CRAFTS ACYLATION REACTION
T Mukaiyama, H Nagaoka, M Ohshima, M Murakami
Index: Mukaiyama, Teruaki; Nagaoka, Hitoshi; Ohshima, Masahiro; Murakami, Masahiro Chemistry Letters, 1986 , p. 165 - 168
Full Text: HTML
Citation Number: 35
Abstract
In the presence of a catalytic amount of diphenylboryl hexachloroantimonate (Ph 2 BSbCl 6), acid chlorides or acid anhydrides react smoothly with aromatic compounds such as anisole and veratrole to give the corresponding aromatic ketones in good yields under mild conditions. Diphenylboryl hexachloroantimonate also activates acyl enolates in the Friedel– Crafts acylation reaction to give the aromatic ketones in good yields under almost neutral ...
Related Articles:
[Suzuki; Kitagawa; Mukaiyama Bulletin of the Chemical Society of Japan, 1993 , vol. 66, # 12 p. 3729 - 3734]
[Suzuki; Kitagawa; Mukaiyama Bulletin of the Chemical Society of Japan, 1993 , vol. 66, # 12 p. 3729 - 3734]