Design, Synthesis, and Evaluation of Ribose-Modified Anilinopyrimidine Derivatives as EGFR Tyrosine Kinase Inhibitors

The synthesis of a series of ribose-modified anilinopyrimidine derivatives was efficiently achieved by utilizing DBU or tBuOLi-promoted coupling of ribosyl alcohols with 2,4,5-trichloropyrimidine as key step. Preliminary biological evaluation of this type of compounds as new EGFR tyrosine kinase inh...

Descripción completa

Detalles Bibliográficos
Autores principales: Hu, Xiuqin, Wang, Disha, Tong, Yi, Tong, Linjiang, Wang, Xia, Zhu, Lili, Xie, Hua, Li, Shiliang, Yang, You, Xu, Yufang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715404/
https://www.ncbi.nlm.nih.gov/pubmed/29250520
http://dx.doi.org/10.3389/fchem.2017.00101

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715404/
https://www.ncbi.nlm.nih.gov/pubmed/29250520
http://dx.doi.org/10.3389/fchem.2017.00101

Ejemplares similares