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Immobilized Ni on TMEDA@βSiO(2)@αSiO(2)@Fe(3)O(4): as a novel magnetic nanocatalyst for preparation of pyrido[2,3-d:6,5-d′]dipyrimidines

In the current body of research, a very quick and effectual procedure for the synthesis of pyrido[2,3-d:6,5-d′]dipyrimidines has been developed. This method is accomplished through the one-pot multi-component reaction of 2-thiobarbituric acid, NH(4)OAc and aldehydes utilizing Ni-TMEDA@βSiO(2)@αSiO(2...

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Detalles Bibliográficos
Autores principales: Almajidi, Yasir Qasim, Ubaidullah, Mohd, Pandit, Bidhan, Kareem, A. K., Romero-Parra, Rosario Mireya, Bobirjon, Adizov, Kadhum, Wesam R., AL-Erjan, Amran M., Abosaooda, Munther, Mahmoud, Aisha Kamal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103747/
https://www.ncbi.nlm.nih.gov/pubmed/37063709
http://dx.doi.org/10.1039/d3ra01720f
Descripción
Sumario:In the current body of research, a very quick and effectual procedure for the synthesis of pyrido[2,3-d:6,5-d′]dipyrimidines has been developed. This method is accomplished through the one-pot multi-component reaction of 2-thiobarbituric acid, NH(4)OAc and aldehydes utilizing Ni-TMEDA@βSiO(2)@αSiO(2)@Fe(3)O(4) as a novel mesoporous nanomagnetic catalyst at room temperature. This protocol is one of the few reports of the preparation of these derivatives without the use of conventional heating as well as energies such as microwave and ultrasound radiation. The characterization of the prepared catalyst was well accomplished by different techniques such as FT-IR, ICP-OES, SEM, TEM, BET, XRD, VSM, TGA, EDX and Elemental mapping. This organometallic catalyst was reusable for seven times with negligible decrement in its catalytic performance. In addition, all of the products were produced with high TON and TOF values, which demonstrates that our catalyst has a very high level of activity in the preparation of pyrido[2,3-d:6,5-d′]dipyrimidines.