Organic Letters · 2024 · 57 citations · 53 references
Natural SciencesChemistryMedicinal ChemistryCatalysisCombinatorial ChemistryOrganic ChemistryDiversity-oriented SynthesisHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsMacrocycle SynthesisOrganic SynthesisAsymmetric Heterocycle SynthesisBicyclononyne ChemistryDiversity-oriented Heterocycle SynthesisMild Reaction ConditionsRing-forming ReactionsSubstrate ScopeSubstrate Scope ExpansionTransformations
= 5 and 6) cycloaddition of bicyclo[1.1.0]butanes (BCBs) with imidazolidines/hexahydropyrimidines is described. The reaction provides a modular, atom-economical, and efficient strategy to two libraries of synthetically challenging medium-bridged rings, 2,5-diazabicyclo[5.1.1]nonanes and 2,6-diazabicyclo[6.1.1]decanes, in moderate to excellent yields. This reaction also features simple operation, mild reaction conditions, and broad substrate scope. A scale-up experiment and various synthetic transformations of products further highlight the synthetic utility.
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Antonia F. Stepan, Chakrapani Subramanyam, Ivan Efremov et al. · Journal of Medicinal Chemistry · 2012 · 446 citations · Full text
Intermolecular [2π+2σ]-photocycloaddition enabled by triplet energy transfer
Roman Kleinmans, Tobias Pinkert, Subhabrata Dutta et al. · Nature · 2022 · 422 citations