Recent advances in ring-forming reactions of donor–acceptor cyclopropanes
Article Properties
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LanguageEnglish
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DOI (url)
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Publication Date2011/11/01
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Journal
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Indian UGC (journal)
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Refrences55
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Citations225
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Mikhail Ya. Mel’nikov
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Ekaterina M. Budynina
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Olga A. Ivanova
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Igor V. Trushkov
Cite
Mel’nikov, Mikhail Ya., et al. “Recent Advances in Ring-Forming Reactions of donor–acceptor Cyclopropanes”. Mendeleev Communications, vol. 21, no. 6, 2011, pp. 293-01, https://doi.org/10.1016/j.mencom.2011.11.001.
Mel’nikov, M. Y., Budynina, E. M., Ivanova, O. A., & Trushkov, I. V. (2011). Recent advances in ring-forming reactions of donor–acceptor cyclopropanes. Mendeleev Communications, 21(6), 293-301. https://doi.org/10.1016/j.mencom.2011.11.001
Mel’nikov, Mikhail Ya., Ekaterina M. Budynina, Olga A. Ivanova, and Igor V. Trushkov. “Recent Advances in Ring-Forming Reactions of donor–acceptor Cyclopropanes”. Mendeleev Communications 21, no. 6 (2011): 293-301. https://doi.org/10.1016/j.mencom.2011.11.001.
Mel’nikov MY, Budynina EM, Ivanova OA, Trushkov IV. Recent advances in ring-forming reactions of donor–acceptor cyclopropanes. Mendeleev Communications. 2011;21(6):293-301.
Journal Categories
Science
Chemistry
Science
Chemistry
General
Including alchemy
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Refrences
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
Lewis Acid‐Catalyzed [3+4] Annulation of 2‐(Heteroaryl)‐ cyclopropane‐1,1‐dicarboxylates with Cyclopentadiene | Advanced Synthesis & Catalysis |
| 52 | 2011 |
| (3 + 3)-Cyclodimerization of Donor–Acceptor Cyclopropanes. Three Routes to Six-Membered Rings | The Journal of Organic Chemistry |
| 70 | 2011 |
| AlCl3-Promoted Highly Regio- and Diastereoselective [3 + 2] Cycloadditions of Activated Cyclopropanes and Aromatic Aldehydes: Construction of 2,5-Diaryl-3,3,4-trisubstituted Tetrahydrofurans | The Journal of Organic Chemistry |
| 75 | 2011 |
| New dimerization and cascade oligomerization reactions of dimethyl 2-phenylcyclopropan-1,1-dicarboxylate catalyzed by Lewis acids | Tetrahedron Letters |
| 51 | 2011 |
| [3+2] Cyclodimerization of 2-arylcyclopropane-1,1-diesters. Lewis acid induced reversion of cyclopropane umpolung | Tetrahedron Letters |
| 41 | 2011 |
Refrences Analysis
The category
Science: Chemistry 32
is the most frequently represented among the references in this article. It primarily includes studies from Organic Letters 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 |
|---|---|---|---|---|
Organocatalytic Enantioselective (4+2) Annulation of Cyclopropane Carbaldehydes with 2‐Mercapto‐1‐Arylethanones | Advanced Synthesis & Catalysis |
| 2024 | |
Synthesis and biological evaluation of 3‐hydroxypyrazoles as aquaporin 9 inhibitors | Journal of Heterocyclic Chemistry |
| 2024 | |
| Alkynyl cyclopropanes in organic synthesis | Russian Chemical Bulletin |
| 2024 | |
| Intramolecular 1,2-Aroyl Migration in Spiro Donor–Acceptor Cyclopropanes: Formation of 1,4-Naphthoquinones and 1-Naphthols as Ring-Expansion Products | The Journal of Organic Chemistry |
| 2024 | |
| Three-Component Synthesis of Substituted Perhydropyrans from β-Styrylmalonates, Aldehydes, and Alkoxyaluminum Dichlorides | Organic Letters |
| 2024 |
Citations Analysis
The category
Science: Chemistry 208
is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled Formation of the double addition products of donor-acceptor cyclopropanes with 2-pyrazolines in the presence of Lewis acids and was published in 2012. The most recent citation comes from a 2024 study titled Intramolecular 1,2-Aroyl Migration in Spiro Donor–Acceptor Cyclopropanes: Formation of 1,4-Naphthoquinones and 1-Naphthols as Ring-Expansion Products. This article reached its peak citation in 2016, with 41 citations. It has been cited in 37 different journals, 10% of which are open access. Among related journals, the Organic Letters cited this research the most, with 39 citations. The chart below illustrates the annual citation trends for this article.