Nucleophilic cyclopropanation of [60]fullerene by the addition–elimination mechanism
Article Properties
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LanguageEnglish
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DOI (url)
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Publication Date2019/01/01
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Journal
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Indian UGC (journal)
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Refrences177
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Citations2
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Yulya N. Biglova Ufa Institute of ChemistryRussian Academy of SciencesUfaRussian FederationDepartment of Chemistry ORCID (unauthenticated)
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Akhat G. Mustafin Ufa Institute of ChemistryRussian Academy of SciencesUfaRussian Federation
Abstract
Cite
Biglova, Yulya N., and Akhat G. Mustafin. “Nucleophilic Cyclopropanation of [60]fullerene by the addition–elimination Mechanism”. RSC Advances, vol. 9, no. 39, 2019, pp. 22428-9, https://doi.org/10.1039/c9ra04036f.
Biglova, Y. N., & Mustafin, A. G. (2019). Nucleophilic cyclopropanation of [60]fullerene by the addition–elimination mechanism. RSC Advances, 9(39), 22428-22498. https://doi.org/10.1039/c9ra04036f
Biglova, Yulya N., and Akhat G. Mustafin. “Nucleophilic Cyclopropanation of [60]fullerene by the addition–elimination Mechanism”. RSC Advances 9, no. 39 (2019): 22428-98. https://doi.org/10.1039/c9ra04036f.
Biglova YN, Mustafin AG. Nucleophilic cyclopropanation of [60]fullerene by the addition–elimination mechanism. RSC Advances. 2019;9(39):22428-9.
Journal Categories
Science
Chemistry
Science
Chemistry
General
Including alchemy
Refrences
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
Poly(ethylene glycol)–[60]Fullerene‐Based Materials for Perovskite Solar Cells with Improved Moisture Resistance and Reduced Hysteresis | ChemSusChem |
| 56 | 2018 |
| Review: Fullerene based acceptors for efficient bulk heterojunction organic solar cell applications | Solar Energy Materials and Solar Cells |
| 234 | 2017 |
| Synthesis of derivatives of fullerenes C 60 and C 70 containing pharmacophore groups | Mendeleev Communications |
| 2 | 2017 |
| TEMPO functionalized C60 fullerene deposited on gold surface for catalytic oxidation of selected alcohols | Journal of Nanoparticle Research |
| 15 | 2017 |
| Synthesis of amino substituted methanofullerenes in the presence of Ti(Oi-Pr)4 | Tetrahedron Letters |
| 6 | 2016 |
Refrences Analysis
The category
Science: Chemistry 125
is the most frequently represented among the references in this article. It primarily includes studies from Tetrahedron Letters and Journal of the American Chemical Society. The chart below illustrates the number of referenced publications per year.
Refrences used by this article by year
Citations
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
[2 + 1] Cycloaddition reactions of fullerene C60 based on diazo compounds | Beilstein Journal of Organic Chemistry |
| 8 | 2021 |
| Sodium-salt adduct fullerenes prevent self-association and amyloid β fibril formation: molecular dynamics approach | Soft Materials |
| 2020 |
Citations Analysis
The category
Science: Chemistry 2
is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled Sodium-salt adduct fullerenes prevent self-association and amyloid β fibril formation: molecular dynamics approach and was published in 2020. The most recent citation comes from a 2021 study titled [2 + 1] Cycloaddition reactions of fullerene C60 based on diazo compounds. This article reached its peak citation in 2021, with 1 citations. It has been cited in 2 different journals, 50% of which are open access. Among related journals, the Beilstein Journal of Organic Chemistry cited this research the most, with 1 citations. The chart below illustrates the annual citation trends for this article.