The Journal of Organic Chemistry · 2016 · 13 citations · 17 references
Natural SciencesChemistryMedicinal ChemistryCrystal StructureOrganic ChemistrySupramolecular ChemistryChiral RecognitionConformational AnalysisConformational ChangeMacromolecular StructureMolecular SymmetrySupramolecular MaterialsChiralityConformational StabilityMolecular Structure DeterminationMolecular Switching BehaviorSolvent PolarityX-ray Diffraction Analysis
N,N'-Diacyl bispidines exhibit chirality in the absence of a chiral center and axis. Conformational analysis indicates planar chirality in the molecular structure as a result of open-ended chiral planes, which has been confirmed by X-ray diffraction studies. Substantial chiral-achiral molecular switching is observed in di(haloacetyl) bispidines upon changing the solvent polarity. Tethering the chiral planes with a bispidine linker alters the planar chirality significantly and renders the resulting bis-bispidine macrocycles achiral.
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