Journal of the American Chemical Society · 2024 · 18 citations · 67 references
Natural SciencesChemistryOrganic ChemistryStructure-activity RelationshipsSynthetic Medicinal ChemistryDiversity-oriented SynthesisHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsMacrocycle SynthesisOrganic SynthesisBicyclononyne ChemistryDiversity-oriented Heterocycle SynthesisElectron-withdrawing GroupsHeterocycle FunctionalizationHeterocyclic MaterialsHeterocyclic ReactivityMacrocyclic Library ConstructionRing-forming Reactions
We report a highly diastereoselective synthesis of polysubstituted bicyclobutanes possessing up to three stereodefined quaternary centers and five substituents. Our strategy involves a diastereoselective carbometalation of cyclopropenes followed by a cyclization to furnish the bicyclobutane ring system. This straightforward approach allows for the incorporation of a diverse range of substituents and functional groups, notably without the need for electron-withdrawing functionalities.
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Ryan Gianatassio, Justin M. Lopchuk, Jie Wang et al. · Science · 2016 · 580 citations
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