TfOH-catalyzed synthesis of 3-aryl isoindolinones via a tandem reaction†
Abstract
A convenient metal-free method for the synthesis of 3-aryl isoindolinones via TfOH catalyzed aromatic C–H functionalization of electron-rich arenes with 2-formylbenzonitriles is developed. This process provided a new efficient strategy for the synthesis of isoindolinone derivatives in good to high yields and regioselectivities by forming two bonds.