TY - JOUR AU - 윤소원 DA - 2016/02 PY - 2016 UR - http://pubs.rsc.org/en/Content/ArticleLanding/2016/OB/C6OB00074F#!divAbstract UR - http://hdl.handle.net/20.500.11754/31885 AB - A highly regioselective synthesis of 3-arylindoles by using the cooperative FeCl3/DDQ system has been developed. This new protocol represents an attractive route for the synthesis of 3-arylindoles from readily accessible non-indole precursors, beta-arylsubstituted 2-styrylanilines, using an inexpensive catalyst and oxidant. Noteworthy is the unique synergetic and synergistic effect of FeCl3 and DDQ on the 1,2-aryl migratory process. PB - ROYAL SOC CHEMISTRY KW - C-H AMINATION KW - 3-SUBSTITUTED INDOLES KW - ANNULATION KW - INHIBITORS KW - PHENOLS KW - ALKENES KW - HYDROAMINATION KW - ACTIVATION KW - CATALYSIS KW - ENAMINES TI - The cooperative FeCl3/DDQ system for the regioselective synthesis of 3-arylindoles from beta-monosubstituted 2-alkenylanilines IS - 7 VL - 14 DO - 10.1039/c6ob00074f T2 - ORGANIC & BIOMOLECULAR CHEMISTRY ER -