Molecular docking, expounding the regiospecificity, stereoselectivity, and the mechanism of [5+2] cycloaddition reaction between ethereal ether and oxidopyrylium-Reference-Cited by-同舟云学术

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

Published:2023-10-12 Issue: Volume: Page:
ISSN:1040-0400
Container-title:Structural Chemistry
language:en
Short-container-title:Struct Chem

Author:

Aitouna Anas Ouled,Mazoir Noureddine,Zeroual Abdellah,Syed Asad,Bahkali Ali H.,Elgorban Abdallah M.,Verma Meenakshi,idrissi Mohammed El,Jasiński Radomir

Publisher

Springer Science and Business Media LLC

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics

Link

https://link.springer.com/content/pdf/10.1007/s11224-023-02239-4.pdf

Reference71 articles.

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2. Jasiński R (2021) On the question of stepwise [4+2] cycloaddition reactions and their stereochemical aspects. Symmetry (Basel) 13(10). https://doi.org/10.3390/sym13101911

3. Aitouna AO, Barhoumi A, Zeroual A (2023) A mechanism study and an investigation of the reason for the stereoselectivity in the [4+2] cycloaddition reaction between cyclopentadiene and gem-substituted ethylene electrophiles. Sci Radices 2(3):217–228. https://doi.org/10.58332/scirad2023v2i3a01

4. El Ghozlani M, Barhoumi A, Elkacmi R, Ouled Aitouna A, Zeroual A, El idrissi M (2020) Mechanistic study of hetero-Diels-Alder [4+2] cycloaddition reactions between 2-nitro-1H-pyrrole and isoprene. Chemistry Africa 3:901–909. https://doi.org/10.1007/s42250-020-00187-8

5. Zahnoune R, Asserne F, Ourhriss N, Ouled Aitouna A, Barhoumi A, Hakmaoui Y, Belghiti ME, Abouricha S, El ajlaoui R, Zeroual A (2022) Theoretical survey of Diels-Alder between acrylic acid and isoprene catalyzed by the titanium tetrachloride and titanium tertafluoride. J Mol Struct 1269:133630. https://doi.org/10.1016/j.molstruc.2022.133630

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