Organic Letters · 2024 · 13 citations · 33 references
Natural SciencesChemistryMedicinal ChemistryCombinatorial ChemistryOrganometallic ChemistryPolymer ChemistryConformational AnalysisConformational ChangeHeterocycle SynthesisMacrocycle SynthesisAsymmetric Heterocycle SynthesisChiralityFragment Coupling StrategyMacrocycle DiscoveryMacrocycle DiversificationReversible Conformational ChangesStereoselective Macrocyclization
Tröger’s base-embedded pillararenes ( P[1]TB[3]A ), which combine Tröger’s base ( TB ) with dialkoxybenzene units, were prepared via a fragment-coupling macrocyclization strategy. The TB unit in macrocycle P[1]TB[3]A provides a fixed chiral source, while 1,4-alkoxybenzene segments flip quickly to change their arrangement, which could provide reversible conformational chirality for those macrocycles. This rare example of macrocycles holding both fixed and conformational chirality lays a good foundation for expanding pillararenes using the fixed chiral source.
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Desymmetrized Leaning Pillar[6]arene
Jia‐Rui Wu, Anthony U. Mu, Bao Li et al. · Angewandte Chemie International Edition · 2018 · 176 citations