The 1,3-dipolar cycloaddition of adamantine-derived nitrones with maleimides
Author:
Affiliation:
1. Institute of Chemistry Saint Petersburg State University, St. Petersburg, Russian Federation;
2. Saint Petersburg Pasteur Institute, St. Petersburg, Russian Federation
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2020.1738494
Reference45 articles.
1. Isoxazolidine: A Privileged Scaffold for Organic and Medicinal Chemistry
2. Design, antiviral and cytostatic properties of isoxazolidine-containing amonafide analogues
3. New Isoxazolidine-Conjugates of Quinazolinones—Synthesis, Antiviral and Cytostatic Activity
4. Regio- and diastereoselectivity of the cycloaddition of aldonitrones with benzylidenecyclopropane: An experimental and theoretical study
5. Highly efficient and stereoselective cycloaddition of nitrones to indolyl- and pyrrolylacrylates
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1. Density Functional Theory Calculations: A Useful Tool to Investigate Mechanisms of 1,3-Dipolar Cycloaddition Reactions;International Journal of Molecular Sciences;2024-01-20
2. Synthesis and Biological Activity of Potential Antiviral Compounds Through 1,3-Dipolar Cycloadditions; Part 2: Nitrones, Nitrile Oxides and Imines, and Other 1,3-Dipoles;Arkivoc;2023-01-04
3. Selective and Reversible 1,3-Dipolar Cycloaddition of 2-(2-Oxoindoline-3-ylidene)acetates with Nitrones in the Synthesis of Functionalized Spiroisoxazolidines;International Journal of Molecular Sciences;2022-10-20
4. The 1,3-dipolar cycloaddition of adamantine-derived nitrones with maleimides: A computational study;Computational and Theoretical Chemistry;2021-01
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