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

3Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free