摘要

A highly regio- and stereoselective hydrochlorination/cyclizationof enynes has been reported by FeCl3 catalysis. A varietyof enynes undergo this cyclization transformation with acetic chlorideas the chlorine source and H2O providing protons via acationic pathway. This protocol provides a cheap, simple, stereospecific,and effective cyclization to afford heterocyclic alkenyl chloridecompounds as Z isomers with high yields (<= 98%)and regioselectivity.

  • 单位
    安徽医科大学