Preparation and NMR properties of derivatives of arylamino-methylidene malonic acid and pentane-2,4-dione
Denisa Tarabová *, Viktor Milata †, Jiří Hanusek ‡ a
Faculty of Chemical and Food Technology, Institute of Organic Chemistry, Slovak University of Technology, Radlinského street 9, SK-812 37 Bratislava, Slovak Republic
a Faculty of Chemical Technology, Department of the Mechanisms of Organic Reactions, University of Pardubice, Student street 95, CZ-532 10 Pardubice, Czech Republic
E-mail: * denisa.tarabova@stuba.sk, † viktor.milata@stuba.sk, ‡ jiri.Hanusek@upce.cz
Abstract: A set of 22 anilinomethylidene derivatives (13 new ones) of di(m)ethyl malonate, malonodinitrile and pentane-2,4-dione with various substituents in position 4- and 3-, respectively were prepared to study the characteristic influence of these substituents and solvents on chemical shifts in 13C NMR spectra and like reference compounds for kinetic measurements.
Keywords: NMR spectroscopy, substituent chemical shifts (SCS), arylaminomethylidene derivatives, enamines
Full paper in Portable Document Format: acs_0148.pdf
Acta Chimica Slovaca, Vol. 6, No. 1, 2013, pp. 73—81, DOI: 10.2478/acs-2013-0013