A three step synthesis of various thiobarbiturate derivatives 17-24 was established. The first step is mediated by Mn(OAc)3, in order to generate a carbon-carbon bond between a terminal alkene and malonate. Derivatives 1-8 were obtained in moderate to good yields under mild conditions. This key step allows synthesis of a wide variety of lipophilic thiobarbiturates, which could be tested for their anticonvulsive or anesthesic potential. © 2012 by the authors.
CITATION STYLE
Bouhlel, A., Curti, C., & Vanelle, P. (2012). New methodology for the synthesis of thiobarbiturates mediated by manganese(III) acetate. Molecules, 17(4), 4313–4325. https://doi.org/10.3390/molecules17044313
Mendeley helps you to discover research relevant for your work.