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Correction

Correction: Pasdar et al. Eco-Friendly Synthesis of Perimidine Derivatives Using Recyclable Fe3O4@Nano-Cellulose/Ti(IV). Molbank 2026, 2026, M2181

by
Ghaffar Pasdar
1,2,*,
Abdolhamid Bamoniri
1,* and
Bi Bi Fatemeh Mirjalili
3
1
Department of Chemistry, College of Science, University of Kashan, Kashan P.O. Box 87317-51167, Iran
2
Institute of Organic Chemistry, Johannes Kepler University Linz, 4040 Linz, Austria
3
Department of Chemistry, College of Science, Yazd University, Yazd P.O. Box 89195-741, Iran
*
Authors to whom correspondence should be addressed.
Molbank 2026, 2026(4), M2208; https://doi.org/10.3390/M2208
Submission received: 20 July 2026 / Revised: 23 July 2026 / Accepted: 27 July 2026 / Published: 3 August 2026
(This article belongs to the Collection Heterocycle Reactions)
In the original publication [1], the following citations were mistakenly included:
2. Zhou, Q.; Wang, M. Nitrogen-containing heterocycles: Versatile synthetic building blocks for pharmaceuticals and agrochemicals. Chem. Soc. Rev. 2012, 41, 3501–3520.
3. Gaba, M.; Singh, S. Recent advances in the medicinal chemistry of imidazole derivatives: Current developments and structure–activity relationships. Eur. J. Med. Chem. 2014, 85, 758–777.
5. Elgemeie, G.H.; Elghandour, A.H.; Abd El-Galil, E. Synthesis and reactions of new perimidine derivatives with potential biological activity. Arch. Pharm. 2000, 333, 197–202.
6. Elgemeie, G.H.; Fahmy, H.H.; Elghandour, A.H. Synthesis and antimicrobial activity of some new perimidine derivatives. Pharmazie 1991, 46, 287–289.
7. Kumar, S.; Bawa, S.; Gupta, H. Biological activities of perimidine derivatives: A review. Med. Chem. 2009, 9, 164–175.
8. Elgemeie, G.H.; Elghandour, A.H.; Fahmy, H.H. Synthesis and antioxidant activity of novel perimidine derivatives. Eur. J. Med. Chem. 2005, 40, 1214–1220.
9. Elgemeie, G.H.; Elghandour, A.H.; Fahmy, H.H. Synthesis and anti-inflammatory activity of perimidine derivatives. Bioorg. Med. Chem. Lett. 2007, 17, 1527–1531.
12. Patil, N.T.; Shinde, V.S.; Gajula, B. N-Heterocyclic carbene-catalyzed multicomponent reactions: A versatile strategy for rapid access to molecular complexity. Chem. Soc. Rev. 2012, 41, 3491–3505.
14. Kumar, S.; Sharma, A.; Maurya, R.A.; Verma, A.K. Multicomponent reactions: A simple and efficient route to bioactive molecules. Chem. Rev. 2021, 121, 13944–14031.
15. Patil, N.T.; Kavthe, R.D.; Shinde, V.S. Gold-catalyzed tandem reactions: An expedient approach to molecular complexity. Chem. Commun. 2014, 50, 14018–14029.
21. Mirjalili, B.F.; Zamani, L. Nano-TiCl4.SiO2: Synthesis of dihydropyrimidinones. S. Afr. J. Chem. 2014, 67, 21–26.
These have now been corrected to the following:
2. Peshkov, V.A.; Pereshivko, O.P.; Van der Eycken, E.V. A walk around the A3-coupling. Chem. Soc. Rev. 2012, 41, 3790–3807.
3. Gaba, M.; Singh, S.; Mohan, C. Benzimidazole: An emerging scaffold for analgesic and anti-inflammatory agents. Eur. J. Med. Chem. 2014, 76, 494–505.
5. Farghaly, T.A.; Mahmoud, H.K. Synthesis, tautomeric structures, and antitumor activity of new perimidines. Arch. Pharm. 2013, 346, 392–402.
6. Elgemeie, G.E.H.; Elghandour, A.H.H. Activated Nitriles in Heterocyclic Synthesis. Novel Synthesis of 5-Imino-5H-[1]benzopyrano[3,4-c]pyridine-4(3H)-thiones and Their Oxo Analogues. Bull. Chem. Soc. Jpn. 1990, 63, 1230–1232.
7. Kumar, S.; Bawa, S.; Gupta, H. Biological activities of quinoline derivatives. Mini Rev. Med. Chem. 2009, 9, 1648–1654.
8. Kotaiah, Y.; Harikrishna, N.; Nagaraju, K.; Rao, C.V. Synthesis and antioxidant activity of 1,3,4-oxadiazole tagged thieno[2,3-d]pyrimidine derivatives. Eur. J. Med. Chem. 2012, 58, 340–345.
9. Saragatsis, M.; Pontiki, E. Synthesis and Antioxidant Activities of Novel Pyrimidine Acrylamides as Inhibitors of Lipoxygenase: Molecular Modeling and In Silico Physicochemical Studies. Molecules 2024, 29, 1189.
12. Patil, N.T.; Shinde, V.S.; Gajula, B. A one-pot catalysis: The strategic classification with some recent examples. Org. Biomol. Chem. 2012, 10, 211–224.
14. Choudhary, A.; Verma, M.; Bharti, R.; Sharma, R. Eco-Friendly and Facile Synthesis of Diverse Heterocycles via Zirconia Nanoparticles Catalyzed One Pot Multicomponent Reaction. Curr. Org. Chem. 2025, 29, 869–885.
15. Kumar, A.; Bhattacharya, N.; Mane, M.V.; Patil, N.T. Ligand-Enabled Gold-Catalyzed Cyanation of Organohalides. Angew. Chem. 2024, 63, e202412682.
21. Mirjalili, B.F.; Zamani, L. Nano-TiCl4.SiO2: A versatile and efficient catalyst for synthesis of dihydropyrimidones via Biginelli condensation. S. Afr. J. Chem. 2014, 67, 21–26.
With this correction, these eleven references have been revised and updated in the online version of the article. The authors state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor. The original publication has also been updated.

Reference

  1. Pasdar, G.; Bamoniri, A.; Mirjalili, B.B.F. Eco-Friendly Synthesis of Perimidine Derivatives Using Recyclable Fe3O4@Nano-Cellulose/Ti(IV). Molbank 2026, 2026, M2181. [Google Scholar] [CrossRef]
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MDPI and ACS Style

Pasdar, G.; Bamoniri, A.; Mirjalili, B.B.F. Correction: Pasdar et al. Eco-Friendly Synthesis of Perimidine Derivatives Using Recyclable Fe3O4@Nano-Cellulose/Ti(IV). Molbank 2026, 2026, M2181. Molbank 2026, 2026, M2208. https://doi.org/10.3390/M2208

AMA Style

Pasdar G, Bamoniri A, Mirjalili BBF. Correction: Pasdar et al. Eco-Friendly Synthesis of Perimidine Derivatives Using Recyclable Fe3O4@Nano-Cellulose/Ti(IV). Molbank 2026, 2026, M2181. Molbank. 2026; 2026(4):M2208. https://doi.org/10.3390/M2208

Chicago/Turabian Style

Pasdar, Ghaffar, Abdolhamid Bamoniri, and Bi Bi Fatemeh Mirjalili. 2026. "Correction: Pasdar et al. Eco-Friendly Synthesis of Perimidine Derivatives Using Recyclable Fe3O4@Nano-Cellulose/Ti(IV). Molbank 2026, 2026, M2181" Molbank 2026, no. 4: M2208. https://doi.org/10.3390/M2208

APA Style

Pasdar, G., Bamoniri, A., & Mirjalili, B. B. F. (2026). Correction: Pasdar et al. Eco-Friendly Synthesis of Perimidine Derivatives Using Recyclable Fe3O4@Nano-Cellulose/Ti(IV). Molbank 2026, 2026, M2181. Molbank, 2026(4), M2208. https://doi.org/10.3390/M2208

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