Synthesis of N-benzyl allylamines by reductive amination with selenophenol generated catalytically

Article abstract of DOI:10.1080/00397919208020849

A convenient method for the preparation of N-benzyl allylamines is described. Selenophenol generated in catalytic quantities from diphenyldiselenide and sodium borohydride leads to the reductive amination of allylamine by substituted benzaldehydes.

Full text of DOI:10.1080/00397919208020849

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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Synthesis of N-Benzyl
Allylamnes by Reductive
Amination with Selenophenol
Generated Catalytically
A. Guy a & J. F. Barbetti a
a Conservatoire National des Arts et
Metiers—Laboratoire de Chimie Organique , URA ,
1103, 292, rue Saint-Martin, 75141, PARIS, Cedex, 03
Published online: 23 Sep 2006.
To cite this article: A. Guy & J. F. Barbetti (1992) Synthesis of N-Benzyl Allylamnes
by Reductive Amination with Selenophenol Generated Catalytically, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 22:6, 853-857, DOI: 10.1080/00397919208020849
To link to this article: http://dx.doi.org/10.1080/00397919208020849
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