Abstract
DFT calculations have been applied to study the mechanisms of [3+2] and [3+2+1] reactions of ene/yne-vinylcyclopropanes (shorted as ene/yne-VCPs). The [3+2] reactions of ene/yne-VCPs start from C-C cleavage of cyclopropane (CP cleavage) to form six-membered rhodacycle, followed by alkene/alkyne insertion and reductive elimination. The [3+2+1] reactions have two competing pathways, one is the [3+2+1] pathway (CP cleavage, ene/yne insertion, CO insertion and reductive elimination) and the other is the [3+1+2] pathway (CP cleavage, CO insertion, ene/yne insertion and reductive elimination). The length of tether in substrates affects the ene/yne insertion steps in these cycloadditions, making some reactions fail or changing the reaction pathways. The reasons for these tether length effects are discussed.
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