1.
Tetrahedron Lett
; 57(14): p. 1592-1596, 2016.
Article
| Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP
| ID: but-ib13767
ABSTRACT
A general and efficient methodology for the synthesis of novel triazoles has been developed based on a microwave-assisted multicomponent reaction involving alpha-thio aldehyde and propargylamine, with the formation of an imine that in situ reacts with organoazides by copper-catalyzed [3+2] azides-alkyne cycloaddition (CuAAC). The reaction results in a small library of imine 1,4-disubstituted 1,2,3-triazoles. (C) 2016 Elsevier Ltd. All rights reserved.