Synthesis of 5-dialkylamino-1,2,3-triazoles and 2-amino-1-azirines From Tertiary Amides
(1980) Tetrahedron Letters — Vol. 21, n° 2, p. 223-226 (1980)
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- Abstract
- The reaction of sodium azide with β-monosubstituted-α-chloroenamines (generated from tertiary amides) yields either 5-dialkylamino-1,2,3-triazoles or 2-amino-1-azirines according to the basicity of the amine substituent.
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Citations
Henriet, M., Houtekie, M., Techy, B., Touillaux, R., & Ghosez, L. (1980). Synthesis of 5-dialkylamino-1,2,3-triazoles and 2-amino-1-azirines From Tertiary Amides. Tetrahedron Letters, 21(2), 223-226. https://doi.org/10.1016/S0040-4039(00)71421-3 (Original work published 1980)