期刊:Synthesis [Thieme Medical Publishers (Germany)] 日期:2015-03-31卷期号:47 (09): 1255-1268被引量:14
标识
DOI:10.1055/s-0034-1380385
摘要
Dual C–C bond formation was accomplished in one pot for the synthesis of a wide variety of indanones mediated by triflic acid. The reaction proceeds via an initial Michael-addition-type Friedel–Crafts alkylation followed by intramolecular acylation (cyclization). Significantly, the method was also successfully employed on more reactive β-diarylcinnamates using slightly different conditions.