Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5261610 | Tetrahedron Letters | 2014 | 6 Pages |
Abstract
An easy and mild two-step one-pot reaction allowed the synthesis of functionalized N-triazolyl maleimide. Next, the addition of propargyl alcohol and propargyl amine to the N-acyliminium ion mediated by Lewis acid, In(OTf)3, allowed the introduction of a second 1,2,3-triazol ring at position 5 of the amide. The products in both reactions were achieved in moderate to good yields.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hélio A. Stefani, Fernando P. Ferreira, Bakhat Ali, Daniel C. Pimenta,