Advanced Synthesis & Catalysis · 2015 · 45 citations · 50 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic SynthesisActivationC-h ActivationFunctional Group ToleranceFused Heterocycle SynthesisHeterocycle FunctionalizationPyridine ChemistryPyridine Synthesis
Abstract A Rh III ‐catalyzed tandem CH activation and CN bond formation reaction between oximes and diazo compounds for the synthesis of heterocycle‐fused pyridine N ‐oxides has been developed. The reaction exhibits good functional group tolerance and regioselectivity. After simple transformation, the 1‐substituted, 1,3‐disubstituted, 1,4‐disubstituted and 1,3,4‐trisubstituted heterocycle‐fused pyridines were all obtained in high efficiency. Moreover, this strategy has also been expanded to the synthesis of a key intermediate for the construction of one potential anti‐HIV agent. magnified image
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Zhuangzhi Shi, Dennis C. Koester, Melissa Boultadakis‐Arapinis et al. · Journal of the American Chemical Society · 2013 · 447 citations