REACTION OF N-ARYLCITRACONISOIMIDIUM PERCHLORATES WITH AROMATIC-HYDROCARBONS UNDER FRIEDEL-CRAFTS CONDITIONS, A NEW AND CONVENIENT ONE-STEPMETHOD FOR THE SYNTHESIS OF BETA-AROYL-ALPHA-ARYL-N-ARYLBUTYRAMIDES
Mf. Ismail et al., REACTION OF N-ARYLCITRACONISOIMIDIUM PERCHLORATES WITH AROMATIC-HYDROCARBONS UNDER FRIEDEL-CRAFTS CONDITIONS, A NEW AND CONVENIENT ONE-STEPMETHOD FOR THE SYNTHESIS OF BETA-AROYL-ALPHA-ARYL-N-ARYLBUTYRAMIDES, Synthetic communications, 26(6), 1996, pp. 1223-1231
A number of beta-Aroyl-alpha-aryl-N-arylbutyramides (<4(a)under bar>-(
h) under bar) have been synthesized using a new methodology involving
arylation at the alpha,beta-unsaturated ketonic systems of N-aryl-citr
aconisoimidium perchlorates (<2(a)under bar>-(c) under bar), followed
by a subsequent ring opening via addition on the carbonyl group to giv
e the title compounds (<4(a)under bar>-(h) under bar).