1-Substituted 5-Aminotetrazoles: Syntheses from CNN3 with Primary Amines
Young-Hyuk Joo and Jean'ne M. Shreeve*
*Department of Chemistry, University of Idaho, Moscow, Idaho
83844-2343, Email: jshreeve
uidaho.edu
Y.-H. Joo, J. M. Shreeve, Org. Lett., 2008, 10, 4665-4667.
DOI: 10.1021/ol8019742
Abstract
The reaction of cyanogen azide and primary amines generates imidoyl azides as intermediates in acetonitrile/water. After cyclization, these intermediates gave 1-substituted aminotetrazoles in good yield.
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Key Words
ID: J54-Y2008-3110
