Abstract
AbstractFrom cyclohexadienyl alkynes with a terminal alkyne unit, double cyclopropanated products were obtained in reasonable to high yields. For cyclohexadienyl alkynes substituted at the alkyne unit, cyclopropanated products were obtained in high yields. When a keto carbonyl group was introduced to cyclohexadienyl alkynes with a substituted alkyne, Alder‐ene‐type products were obtained in reasonable to high yields.
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