Recent advances in the chemistry of selenophenopyrimidine heterocycles: Synthesis, reactivity, and biological activity

被引:1
|
作者
Helal, Mohamed H. [1 ]
Salem, Mohamed A. [2 ]
Gouda, Moustafa A. [3 ,4 ]
机构
[1] Northern Border Univ, Fac Arts & Sci, Dept Chem, Rafha 91911, Saudi Arabia
[2] King Khalid Univ, Fac Sci & Arts, Dept Chem, Mohail Asir, Saudi Arabia
[3] Taibah Univ, Coll Sci, Dept Chem, Al Madinah Al Munawarah 30002, Saudi Arabia
[4] Mansoura Univ, Fac Sci, Dept Chem, Mansoura 35516, Egypt
关键词
Vilsmeier-Haack reagent; Gewald reaction; Suzuki cross-coupling; Synthesis; Biological activity; Reactivity; ANTICANCER ACTIVITY; SELENOPHENE; DERIVATIVES; ANALOGS; FACILE; ROUTE;
D O I
10.1016/j.jorganchem.2024.123343
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Undoubtedly, pyrimidine and selenophene stand as invaluable heterocyclic compounds pivotal in the quest for novel drug development. The fusion of selenophene and pyrimidine motifs into hybrid architectures has ushered in a realm of promising pharmacological potentialities. This amalgamation has given rise to selenophenopyrimidine derivatives, such as selenopheno[2,3-d]pyrimidine, d ]pyrimidine, selenopheno[3,4-d]pyrimidine, d ]pyrimidine, and selenopheno [3,2-d]pyrimidine, d ]pyrimidine, each boasting intriguing properties. Synthesizing selenophenopyrimidines encompasses diverse chemical pathways, including one-pot multi-component reactions, Vilsmeier-Haack reactions, Gewald reactions, and Suzuki cross-coupling methodologies.
引用
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页数:25
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