Reaction of 2-cyanoethane-1,1,2-tricarboxamide with α-alkylacroleins

Autor: Nasakin, O. E., Pavlov, V. V., Lyshchikov, A. N., Lukin, P. M., Khrustalev, V. N., Antipin, M. Yu., Urman, Ya. G.
Zdroj: Chemistry of Heterocyclic Compounds; October 1996, Vol. 32 Issue: 10 p1136-1140, 5p
Abstrakt: In the presence of catalytic amounts of triethylamine 2-cyanoethane-1,1,2-tricarboxamide forms Michael adducts with a-alkylacroleins. After two intramolecular cyclizations, the adducts are converted into 5-alkyl-6-amino-4-hydroxy-7-carbamoyl-2-oxo-1-cyano-3-azabicyclo[3.2.1]oct-6-enes.
Databáze: Supplemental Index