Reactions of N-nitrosodiphenylamine with Grignard reagents. A convenient synthesis of diaryl- and dialkyl nitroxyls

Article abstract of DOI:10.1080/00397919208021294

N-nitrosodiphenylamine reacts with Grignard reagents forming symmetric dialkyl- or diarylhydroxylamines which are quantitatively converted into the corresponding nitroxyls by lead dioxide oxidation.

Full text of DOI:10.1080/00397919208021294

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Synthetic Communications: An
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Reactions of N-
Nitrosodiphenylamine
with Grignard Reagents. A
Convenient Synthesis of Diaryl-
and Dialkyl Nitroxyls
Liberato Cardellini a , Lucedio Greci a & Giorgio Tosi
a
a Dipartimento di Scienze dei Materiali e della Terra,
Università, via Brecce Bianche 60131, Ancona, Italy
Published online: 23 Sep 2006.
To cite this article: Liberato Cardellini , Lucedio Greci & Giorgio Tosi (1992) Reactions
of N-Nitrosodiphenylamine with Grignard Reagents. A Convenient Synthesis of Diaryl-
and Dialkyl Nitroxyls, Synthetic Communications: An International Journal for Rapid
Communication of Synthetic Organic Chemistry, 22:2, 201-207
To link to this article: http://dx.doi.org/10.1080/00397919208021294
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