Published 2012-06-02
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Brief communication

Reactividad del Aminal Macrociclico1:3,7:9,13:15,19:21- Tetrametilentetrahexahidropirimidina (Tmtp) con Fenoles P-Sustituidos

DOI: https://doi.org/10.22490/25394088.1113
Daniel Jesús Alcázar Franco Universidad de la Costa, Barranquilla, Colombia.
Claudia Patricia Herrera Herrera Universidad de la Costa, Barranquilla, Colombia.
Fabio Armando Fuentes Gandara Universidad de la Costa, Barranquilla, Colombia.

Una nueva serie de compuestos de estructuras tipo 1,3-hexahidropirimidina se logró sintetizar, con el fin de comprobar y ratificar la reactividad del aminalmacrociclico: 1:3,7;9,13;15,19;21-tetrametilentetrahexahidropirimidina (TMTP) con fenoles para-sustituidos, empleando reacciones tipo Mannich en
medio alcalino. Las estructuras se elucidaron por métodos espectroscópicos, las cuales mostraron compuestos consistentes con las estructuras propuestas. Los compuestos sintetizados no se encuentran reportados en la literatura consultada.

keywords: bases di-Mannich, hexahidropirimidina, macrociclo, sustituido fenol
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How to Cite
Alcázar Franco, D. J., Herrera Herrera, C. P., & Fuentes Gandara, F. A. (2012). Reactividad del Aminal Macrociclico1:3,7:9,13:15,19:21- Tetrametilentetrahexahidropirimidina (Tmtp) con Fenoles P-Sustituidos. Publicaciones E Investigación, 6, 131-138. https://doi.org/10.22490/25394088.1113
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