Journal of the American Chemical Society · 2019 · 144 citations · 40 references
Natural SciencesChemistryCombinatorial ChemistryOrganic ChemistryPolymer ChemistryHeterocycle SynthesisHeterocyclic ChemistryAlkyne Cycloaddition ReactionsChiralityCyclotrimerization Of AlkynesEnantiomeric Purity AssessmentEnantiomeric SeparationGibbs Free Energy
A belt-shaped [8]cycloparaphenylene (CPP) and an enantioenriched Möbius-shaped [10]CPP have been synthesized by high-yielding rhodium-catalyzed intramolecular cyclotrimerizations of a cyclic dodecayne and a pentadecayne, respectively. This Möbius-shaped [10]CPP possesses stable chirality and isolated with high enantiomeric purity. It is evident from the reaction Gibbs energy calculation that the above irreversible cyclotrimerizations are highly exothermic; therefore establishing that the intramolecular alkyne cyclotrimerization is a powerful route to strained cyclic molecular strips.
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