Nucleophilic Aromatic Substitution of 5-Bromo-1,2,3-triazines with Phenols
Nucleophilic aromatic substitution (S Ar) reaction in classic textbook is a stepwise mechanism, and few examples of concerted reactions have been reported. Herein, we developed a concerted S Ar reaction of 5-bromo-1,2,3-triazines with phenols in which the nonclassic mechanism of this reaction could...
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Veröffentlicht in: | Journal of organic chemistry 2022-03, Vol.87 (5), p.2590-2600 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Nucleophilic aromatic substitution (S
Ar) reaction in classic textbook is a stepwise mechanism, and few examples of concerted reactions have been reported. Herein, we developed a concerted S
Ar reaction of 5-bromo-1,2,3-triazines with phenols in which the nonclassic mechanism of this reaction could be revealed by calculation. Furthermore, the resulting 5-aryloxy-1,2,3-triazines could be used as convenient precursors to access biologically important 3-aryloxy-pyridines in one-pot manner. |
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ISSN: | 0022-3263 1520-6904 |
DOI: | 10.1021/acs.joc.1c02543 |