A facile synthesis of 1,2,3-triazolyl indole hybrids via SbCl3-catalysed Michael addition of indoles to 1,2,3-triazolyl chalcones

18Citations
Citations of this article
14Readers
Mendeley users who have this article in their library.
Get full text

Abstract

An efficient, facile and environmentally benign synthesis of a library of 1,2,3-triazolyl chalcone hybrids (3a-u) has been accomplished by grinding the reactants at room temperature in excellent yields in very short reaction time. Subsequently, SbCl3 catalysed Michael addition of indoles to the chalcones afford 1,2,3-triazolyl indole hybrids (5a-l) in excellent yields. © Indian Academy of Sciences.

Cite

CITATION STYLE

APA

Shanmugavelan, P., Sathishkumar, M., Nagarajan, S., & Ponnuswamy, A. (2012). A facile synthesis of 1,2,3-triazolyl indole hybrids via SbCl3-catalysed Michael addition of indoles to 1,2,3-triazolyl chalcones. Journal of Chemical Sciences, 124(4), 941–950. https://doi.org/10.1007/s12039-012-0281-x

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