Abstract
A straightforward approach to novel fused β-carbolines namely [1,3,5]triazino [1',2':1,6]pyrido[3,4-b]indol-4-ones is presented. The construction of these compounds was achieved by one-pot synthesis involving condensation of 3-amino-β-carbolines with ethoxycarbonyl isothiocyanate followed by amination of the resulting thioureas and finally thermal ring closure of the resulting guanidines which allowed access to the unreported title heterocycles. © ARKAT USA, Inc.
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Primas, N., El-Kashef, H., Lancelot, J. C., Lesnard, A., Dodd, R. H., & Raulta, S. (2010). Triazine-fused β-carbolines: A facile three-step, one-pot synthesis of novel 2-alkyl(aryl)amino and 2-dialkylamino-7H-[1,3,5]triazino [1’,2’:1,6]pyrido[3,4-b]indol-4-ones. Arkivoc, 2010(11), 163–176. https://doi.org/10.3998/ark.5550190.0011.b14
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