A simple, efficient, and high yielding one-pot protocol for the synthesis of novel highly substituted α-acyloxycarbox-amidobarbiturates has been developed by a three-component reaction of alloxans, various carboxylic acids, and alkyl or aryl isocyanides in acetonitrile at room temperature.
DundeeJ.W., and McIlroyP.D.A., Anaesthesia, 1982, 37, 726.
2.
López-MunozF., Ucha-UdabeR., and AlamoC., Neuropsychiatr. Dis. Treat., 2005, 1, 329.
3.
CharneyD.S., MihicS.J., and HarrisR.A., eds HardmanJ.G., and LimbirdL.E., Goodman & Gilman's The pharmacological basis of therapeutics.2001, 10th edn. McGraw Hill, New York, pp. 399–427.
4.
WilbergerJ.E., and CantellaD., New Horiz., 1995, 3, 469.
KingS.B., StratfordE.S., CraigC.R., and FiferE.K., Pharmaceut. Res., 1995, 12, 1240.
7.
VidaJ.A., and GerryE.H., Anticonvulsants-medicinal chemistry. A series of monographs, eds VidaJ.A., Vol. 15, Academic Press, New York, 1977, pp. 151–173.
8.
AndrewsP.R., JonesG.P., and LodgeD., Eur. J. Pharmacol., 1979, 55, 115.
9.
AndrewsP.R., JonesG.P., and PoultonD.B., Eur. J. Pharmacol., 1982, 79, 61.
10.
CupidoT., Tulla-PucheJ., SpenglerJ., and AlbericioF., Curr. Opin. Drug Discov. Devel., 2007, 10, 768.
11.
BodeJ.W., Curr. Opin. Drug Disco. Devel., 2006, 9, 765.
12.
HumphreyJ.M., and ChamberlinA.R., Chem. Rev, 1997, 97, 2243.
13.
TianF.-F., ZhouP., and LiZ.-L., J. Mol. Struct., 2007, 830, 106.