E—Z-Izomerization of 2-methylenethiazolidin-4-ones.

Autor: Morzherin, Yu., Kosterina, M., Berseneva, V., Dehaen, W., Bakulev, V.
Zdroj: Russian Chemical Bulletin; Jul2002, Vol. 51 Issue 7, p1292-1297, 6p
Abstrakt: The equilibrium concentrations of E- and Z-isomers of thiazolidin-4-ones containing exocyclic double bonds in positions 2 and 5 of the cycle were determined in DMSO-d6. The influence of the nature of the substituents on the equilibrium position was found. Electron-releasing substituents stabilize the E, Z-configuration and electron-withdrawing substituents stabilize the Z, Z-configuration. The association constants of E- and Z-2-ethoxycarbonylmethylenethiazolidin-4-ones with the sodium cation were determined by 1H NMR spectroscopy. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index