In the reaction of dimethyl phosphite anion with 1-nitronaphthalene, nucleophilic substitution of hydrogen takes place according to a redox stoicheiometry, giving substituted dimethyl naphthalenephosphonates and benzazepines; other bicyclic nitroarenes react in a similar way.
W. Danikiewicz and M. Makosza, J. Chem. Soc., Chem. Commun., 1985, 1792 DOI: 10.1039/C39850001792
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