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 CH 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 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We report Pd‐ and Ni‐catalysed, guided and regioselective CH 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 CH 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. |
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ISSN: | 1867-3880 1867-3899 |
DOI: | 10.1002/cctc.201402715 |