New experiments in the reductive N-alkylation and N-peralkylation of aromatic amines

Article abstract of DOI:10.1080/00397919408012638

Some secondary and primary aromatic amines were variously N-alkylated and N-peralkylated by the aldehyde-sodium borohydride procedure in acidic aqueous solution. The procedure lends itself to the α-mono and α,α¹-dideuterium labelling of the new N-substituent(s).

Full text of DOI:10.1080/00397919408012638

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Synthetic Communications: An
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New Experiments in the
Reductive N-Alkylation and
N-Peralkylation of Aromatic
Amines
G. Verardo a , A. G. Giumanini a & P. Strazzolini a
a Department of Chemical Sciences and
Technologies, University of Udine, I-33100, Udine,
Italy
Version of record first published: 23 Sep 2006.
To cite this article: G. Verardo, A. G. Giumanini & P. Strazzolini (1994): New
Experiments in the Reductive N-Alkylation and N-Peralkylation of Aromatic Amines,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 24:5, 609-627
To link to this article: http://dx.doi.org/10.1080/00397919408012638
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