TiCl4 induced N-methyleneamine equivalents: A new route to aminoacetonitriles

Article abstract of DOI:10.1080/00397919108020806

TiCl₄ induced N-methyleneamine equivalents from hexahydro-1,3,5-triazines or N-(methoxymethyl)amines were reacted with trimethylsilyl cyanide to give aminoacetonitriles in 40-90% yield.

Full text of DOI:10.1080/00397919108020806

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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TiCl4 induced N-
Methyleneamine
Equivalents: A New Route to
Aminoacetonitriles
Hyun-Joon Ha a , Gong-Sil Nam a & Kyong Pae Park a
a Division of Chemistry, Korea Institute of Science
and Technology, P.O. Box 131 Cheongryang, Seoul,
130-650, Korea
Published online: 23 Sep 2006.
To cite this article: Hyun-Joon Ha , Gong-Sil Nam & Kyong Pae Park (1991) TiCl4
induced N-Methyleneamine Equivalents: A New Route to Aminoacetonitriles, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 21:2, 155-160, DOI: 10.1080/00397919108020806
To link to this article: http://dx.doi.org/10.1080/00397919108020806
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