Recent advances in the chemistry of selenophenofurans and their analogues

被引:0
作者
Helal, Mohamed H. [1 ]
Jame, Rasha [2 ]
Salem, Mohamed A. [3 ]
Gouda, Moustafa A. [4 ,5 ]
机构
[1] Northern Border Univ, Ctr Sci Res & Entrepreneurship, Ar Ar 73213, Saudi Arabia
[2] Univ Tabuk, Fac Sci, Dept Chem, Tabuk 71491, Saudi Arabia
[3] king khalid Univ, Appl Coll, Hlth Specialties Basic Sci & Their Applicat Unit, Abha 61421, Saudi Arabia
[4] Taibah Univ, Coll Sci, Dept Chem, Al Madinah Al Munawarah 30002, Saudi Arabia
[5] Mansoura Univ, Fac Sci, Dept Chem, Mansoura 35516, Egypt
关键词
Suzuki-miyaura; Stille; And sonogashira coupling reactions; Selenation reactions; Cyclization reactions; Synthesis; reactivity; HETEROCYCLES; DERIVATIVES; CYCLIZATION; ROUTE;
D O I
10.1016/j.jorganchem.2025.123721
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The fusion of furan and selenophene in hybrid configurations results in four distinct structural types: condensed 1H,3H-selenopheno[3,4-c]furans, selenopheno[3,4-b]furans, selenopheno[2,3-b]furans, and selenopheno[3,2-b] furans. Despite their potential, no dedicated studies have exclusively explored this scaffold, which has primarily been employed as a versatile building block across various applications. The synthesis of selenophenofurans and their analogs can be achieved through diverse chemical approaches, including (i) selenation reactions, (ii) Suzuki-Miyaura coupling, (iii) Stille and Sonogashira coupling, and (iv) cyclization reactions, among other methods.
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页数:22
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