作者:Richard A Decréau、James P Collman
DOI:10.1016/s0040-4039(03)00617-8
日期:2003.4
A3 and trans-A2B tris-aryl corroles 1a–c have been synthesized in up to 12% yield by BF3·Et2O-catalyzed condensation of dipyrromethane–dicarbinol and 2,2′-bipyrrole (1:1 ratio) in acetonitrile at room temperature for 24 h.
BF 3 ·Et 2 O催化二吡咯甲烷-二咔啉与2,2'-联吡咯(1:1比例)的合成,可合成高达3%的A 3和反式A 2 B三芳基芳烃1a – c)在室温下于乙腈中放置24小时。