64500-71-6Relevant academic research and scientific papers
A simple synthesis of enaminones from reaction between isocyanides and cyclic 1,3-dicarbonyl compounds
Maghsoodlou, Malek Taher,Hazeri, Nourallah,Habibi-Khorassani, Sayyed Mostafa,Solimani, Vahideh,Marandi, Ghasem,Razmjoo, Zahra
experimental part, p. 198 - 200 (2009/09/06)
Polarised olfinic systems are synthesised from the reaction between alkyl or aryl isocyanides and cyclic 1, 3-dicarbonyl compounds such as thiobarbituric acid, 5,5-dimethylcyclohexane-1,3-dione and cyclopentane-1,3-dione in good yield.
ACETALS OF LACTAMS AND ACID AMIDES. 48. REACTION OF ENAMINO DIKETONES WITH AMIDE ACETALS. SYNTHESIS OF DERIVATIVES OF COUMARIN AND CARBOSTYRIL
Grannik, V. G.,Shanazarov, A. K.,Solov'eva, N. P.,Chistyakov, V. V.,Persianova, I. V.,Sheinker, Yu. N.
, p. 1171 - 1177 (2007/10/02)
It was established that the reaction of derivatives of 2-aminomethylenecyclohexane-1,3-dione with N,N-dimethyl-diethylacetal gives dienediamines, heating of which in aqueous hydrochloric acid leads, depending on the structure, to derivatives of carbostyri
TRANSAMINATION OF TERTIARY ENAMINES, SYNTHESIS OF β-SUBSTITUTED N-BENZYLENAMINES
Granik, V. G.,Zhidkova, A. M.,Zhivotovskaya, I. S.,Solov'eva, N. P.,Polievktov, M. K.
, p. 2163 - 2166 (2007/10/02)
The rate constants for the transamination of tertiary enamines by means of benzylamine were measured by polarography.The PMR spectra of the obtained compounds indicate the presence of strong intramolecular hydrogen bonds, due to the presence of the NH gro
