Advanced Synthesis & Catalysis · 2006 · 62 citations · 25 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic SynthesisAutooxidationElectron-rich ComplexesIndolizine ChemistryPyridine ChemistryPyridine SynthesisQuinoline Synthesis
Abstract The formal [3+2] dipolar cycloaddition (or annulation) of donor‐acceptor cyclopropanoate esters with pyridines and 5‐nitroquinoline is reported. Electron‐deficient pyridine dipolarophiles (R=CN, CO 2 Et, COMe) participate in the annulation whereas electron rich species do not. The product 2,3‐dihydroindolizines undergo rapid autooxidation, and the X‐ray structures for two of the aromatic products are reported.
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Palladium-Catalyzed Arylation and Heteroarylation of Indolizines
Choul‐Hong Park, Victoria Ryabova, Anna W. Sromek et al. · Organic Letters · 2004 · 299 citations
Oxycyclopropanes in organochemical synthesis
Ernest Wenkert · Accounts of Chemical Research · 1980 · 239 citations