Triethylamine-Mediated Generation of a Synthetic Equivalent of Parent Azomethine Imine by Condensation of Ethyl 3-Benzylcarbazate with Paraformaldehyde
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[1] S. Kanemasa,et al. Lithium bromide-triethylamine induced cycloaddition of N-alkylidene 2-amino esters and amides to electron-deficient olefins with high regio- and stereoselectivity , 1988 .
[2] R. Grigg,et al. Prototropic routes to 1,3- and 1,5-dipoles, and 1,2-ylides: applications to the synthesis of heterocyclic compounds , 1987 .
[3] A. Packard,et al. Intra- and intermolecular cyclization of olefinic tosylhydrazones under acidic conditions. A facile synthesis of bicyclic azoalkanes , 1980 .
[4] J. Hamelin,et al. Addition d'hydrazone aux oléfines en milieu acide: cycloaddition polaire cationique [3+ + 2] , 1979 .
[5] J. Lown,,et al. Further Synthetic Applications of Functionalized 1,3-Dipoles , 1975 .
[6] M. V. George,et al. Reactions of dimethyl acetylenedicarboxylate—VI : Reaction with aldehyde and ketone phenylhydrazones , 1973 .
[7] K. Hesse. Synthese von Pyrazolidinen , 1971 .