Abstract
The cycloaddition reactions involving dichlorocarbene generated under phase transfer conditions have been studied extensively in the past few years due to the simplicity of the procedure involved.1 The facile formation of dichlorocyclopropanes provides an easy entry to functionalised aromatics and expanded carbocyclic compounds.2 The dichlorocarbene generated under phase transfer conditions is capable of adding even to electron deficient olefins. We describe here the cyclo-addition reaction of dichlorocarbene to tetrasubstituted cyclopentadienones.