Regioselective Direct Arylation of Fused 3-Nitropyridines and Other Nitro-Substituted Heteroarenes: The Multipurpose Nature of the Nitro Group as a Directing Group

We report Pd‐ and Ni‐catalysed, guided and regioselective CH arylations of a series of fused 3‐nitropyridines. The method described here is a facile tool for the chemical functionalisation of drug‐like fused pyridines. The scope and limitations of the reaction, the chemical potential of the nitro g...

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Veröffentlicht in:ChemCatChem 2015-01, Vol.7 (2), p.316-324
Hauptverfasser: Iaroshenko, Viktor O., Gevorgyan, Ashot, Mkrtchyan, Satenik, Grigoryan, Tatevik, Movsisyan, Ester, Villinger, Alexander, Langer, Peter
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Sprache:eng
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Zusammenfassung:We report Pd‐ and Ni‐catalysed, guided and regioselective CH arylations of a series of fused 3‐nitropyridines. The method described here is a facile tool for the chemical functionalisation of drug‐like fused pyridines. The scope and limitations of the reaction, the chemical potential of the nitro group and a putative reaction mechanism are discussed. So nitro: We report Pd‐ and Ni‐catalyzed, guided, and regioselective CH arylations of a series of fused 3‐nitropyridines. The method described here is a facile tool for the chemical functionalization of drug‐like fused pyridines. The scope and limitations of the reaction, the chemical potential of the nitro group, and a putative reaction mechanism are discussed.
ISSN:1867-3880
1867-3899
DOI:10.1002/cctc.201402715