Quantum mechanical modeling unveils the effect of substitutions on the activation barriers of the Diels–Alder reactions of an antiviral compound 7H-benzo[a]phenalene-Reference-Cited by-同舟云学术

Quantum mechanical modeling unveils the effect of substitutions on the activation barriers of the Diels–Alder reactions of an antiviral compound 7H-benzo[a]phenalene

Published:2022-05-10 Issue:6 Volume:33 Page:1907-1920
ISSN:1040-0400
Container-title:Structural Chemistry
language:en
Short-container-title:Struct Chem

Author:

Rehman Umatur,Mansha Asim^ORCID,Zahid Muhammad,Asim Sadia,Zahoor Ameer Fawad,Rehan Zulfiqar Ahmad

Funder

Higher Education Commision, Pakistan

Publisher

Springer Science and Business Media LLC

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics

Link

https://link.springer.com/content/pdf/10.1007/s11224-022-01948-6.pdf

Reference81 articles.

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2. Samba WK, Tia R, Adei E (2021) Regio-, enantio-, peri-, and stereo-selectivities of the reactions of five-membered cyclodiene derivatives with itaconic anhydride toward the formation of norbornene lactones. J Phys Org Chem 34(2):e4132. https://doi.org/10.1002/poc.4132

3. Khan TS, Gupta S, Ahmad M, Alam MI, Haider MA (2020) Effect of substituents and promoters on the Diels-Alder cycloaddition reaction in the biorenewable synthesis of trimellitic acid. RSC Adv 10(51):30656–30670. https://doi.org/10.1039/D0RA04318D

4. Oluwasanmi A, Hoskins C (2021) Potential use of the Diels-Alder reaction in biomedical and nanomedicine applications. Int J Pharm 604:120727. https://doi.org/10.1016/j.ijpharm.2021.120727

5. Medrán NS, Dezotti F, Pellegrinet SC (2019) Remarkable reactivity of boron-substituted furans in the Diels-Alder reactions with maleic anhydride. Org Lett 21(13):5068–5072. https://doi.org/10.1021/acs.orglett.9b01662

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