Molecular docking, expounding the regiospecificity, stereoselectivity, and the mechanism of [5+2] cycloaddition reaction between ethereal ether and oxidopyrylium

被引:1
|
作者
Aitouna, Anas Ouled [1 ,2 ]
Mazoir, Noureddine [2 ]
Zeroual, Abdellah [1 ]
Syed, Asad [3 ]
Bahkali, Ali H. [3 ]
Elgorban, Abdallah M. [3 ]
Verma, Meenakshi [4 ]
Idrissi, Mohammed El [5 ]
Jasinski, Radomir [6 ]
机构
[1] Chouaib Doukkali Univ, Fac Sci, Mol Modelling & Spect Res Team, POB 20, El Jadida 24000, Morocco
[2] Univ Chouaib Doukkali, Dept Chem, Fac Sci, Lab Bioorgan Chem, POB 20, El Jadida 24000, Morocco
[3] King Saud Univ, Coll Sci, Dept Bot & Microbiol, POB 2455, Riyadh 11451, Saudi Arabia
[4] Chandigarh Univ Gharuan, Univ Ctr Res & Dev, Dept Chem, Mohali, India
[5] Sultan Moulay Slimane Univ, Fac Polydisciplinary, Team Chem Proc & Appl Mat, Beni Mellal, Morocco
[6] Cracow Univ Technol, Dept Organ Chem & Technol, Warszawska 24, PL-31155 Krakow, Poland
关键词
5+2] cycloaddition; MEDT; Regiospecificity; DFT; ELF; Oxidopyrylium; ELECTRON-DENSITY THEORY; LOCALIZATION; STEPWISE; ALKENES;
D O I
10.1007/s11224-023-02239-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Application of molecular electron density theory (MEDT) to investigate the [5+2] cycloaddition reaction between oxidopyrylium and ethervinylether, we discovered that oxidopyrylium is an electrophile and ethervinylether is a nucleophile by an examination of conceptual DFT indices. Analysis of energetical parameters shows clearly that this cycloaddition is both regio- and stereoselective, which is extremely consistent with the experience. Topological analysis of the electron localization function (ELF) has shown that this [5+2] cycloaddition is achieved by a two-step, single-step mechanism along the most favored route. Aside from that, docking outcomes show that the (1-20) oxabicyclo[3.2.1]octene derivatives have a significant anti-HIV potential.
引用
收藏
页码:841 / 852
页数:12
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