Synthetic routes for N-arylation of carbazole derivatives and their applications as organic materials

被引:1
|
作者
Mukhtar, Sobia [1 ]
Rafiq, Ayesha [1 ]
Naqvi, Syed Ali Raza [1 ]
Aslam, Sana [2 ]
Ahmad, Matloob [1 ]
Al-Hussain, Sami A. [3 ]
Zaki, Magdi E. A. [3 ]
机构
[1] Govt Coll Univ Faisalabad, Dept Chem, Faisalabad 38000, Pakistan
[2] Govt Coll Women Univ Faisalabad, Dept Chem, Faisalabad 38000, Pakistan
[3] Imam Mohammad Ibn Saud Islamic Univ IMSIU, Coll Sci, Dept Chem, Riyadh 11623, Saudi Arabia
关键词
Carbazole; N-arylation; Synthesis; Reaction; Catalyst; Applications; MONOAMINE-OXIDASE INHIBITION; MURRAYA-KOENIGII; COUPLING REACTIONS; PRIMARY AMINES; ANTIPROLIFERATIVE ACTIVITY; BIOLOGICAL-ACTIVITY; MOLECULAR DOCKING; HOST MATERIALS; ARYL IODIDES; IN-VITRO;
D O I
10.1016/j.jscs.2024.101927
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbazole is a heterocyclic aromatic organic compound that has vast applications in pharmaceuticals, and in biological and material sciences. Carbazole derivatives show various biological activities such as antibiotic, antiinflammatory, anti-tumor and anti-oxidant activities etc. . Synthesis of N-arylated carbazoles has become a major area of interest for scientists due to their applications in organic light-emitting diodes, dye-sensitized solar cells, and other organic electronics. The N-arylated carbazoles have unique properties such as high thermal stability, wide band gap, and excellent electrical and optical properties. The methods used for the N-arylation of carbazoles include transition metal-catalyzed reactions and metal-free reactions. The most common and classical methods for the N-arylation of carbazoles are copper-catalyzed Ullmann coupling reactions, while palladium, nickel, and iron catalysts are also used. This review focuses on all the synthetic methods used for the N-arylation of carbazoles and their applications.
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页数:36
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