Journal of the Chemical Society Chemical Communications · 1973 · 14 citations · 0 references
Natural SciencesChemistryOrganic ChemistryAddition ReactionsHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic Synthesis[4+2] CycloadditionCyclopropanation ReactionsDouble Bond ConfigurationHeterocyclic ReactivityRegioselectivity In Cycloadditions
Two alternative modes of addition to vinyl-cyclopropane systems are here described for each of two dienophiles: tetracyanoethylene is shown to react either via[2 + 2] or by [2 + 4] cycloadditions; and dimethyl acetylenedicarboxylate reacts either by the ‘ene’ route or by way of insertion to the double bond.