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For: Ludwig BS, Correia JD, Kühn FE. Ferrocene derivatives as anti-infective agents. Coordination Chemistry Reviews 2019;396:22-48. [DOI: 10.1016/j.ccr.2019.06.004] [Cited by in Crossref: 26] [Cited by in F6Publishing: 34] [Article Influence: 8.7] [Reference Citation Analysis]
Number Citing Articles
1 dos Santos Filho JM, de Souza Castro MVB. Synthesis, structural characterization, and antimicrobial activity of novel ferrocene-N-acyl hydrazones designed by means of molecular simplification strategy Celebrating the 100th anniversary of the birth of Professor Paulo Freire. Journal of Organometallic Chemistry 2022;979:122488. [DOI: 10.1016/j.jorganchem.2022.122488] [Reference Citation Analysis]
2 Das S, Borkotoky S, Rymbai M, Borah VV, Roy JD, Kaping S, Helissey P, Vishwakarma JN. Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids: A facile environment-friendly regioselective synthesis, structure elucidation, and their antioxidant, antibacterial, and anti-biofilm activities. J Chem Sci 2022;134. [DOI: 10.1007/s12039-022-02064-y] [Reference Citation Analysis]
3 Suzuki N, Yoneyama S, Sato K, Shiba K, Nakayama T, Uematsu Y, Sakurai K. Synthesis of O,N,O-P-multidentate ligands and their heterobimetallic complexes. Journal of Organometallic Chemistry 2022. [DOI: 10.1016/j.jorganchem.2022.122531] [Reference Citation Analysis]
4 Poje G, Marinović M, Pavić K, Mioč M, Kralj M, de Carvalho LP, Held J, Perković I, Rajić Z. Harmicens, Novel Harmine and Ferrocene Hybrids: Design, Synthesis and Biological Activity. IJMS 2022;23:9315. [DOI: 10.3390/ijms23169315] [Reference Citation Analysis]
5 Ranjan A, Sharma D, Srivastava AK, Varma A, Magani SK, Joshi RK. Evaluation of anticancer activity of ferrocene based benzothiazole and β-ketooxothioacetal. Journal of Organometallic Chemistry 2022. [DOI: 10.1016/j.jorganchem.2022.122500] [Reference Citation Analysis]
6 Gupta A, Das R, Chamoli A, Choithramani A, Kumar H, Patel S, Khude D, Bothra G, Wangdale K, Ghosh Chowdhury M, Rathod R, Mandoli A, Shard A. A Series of Ferrocene-Containing Pyrazolo[1,5- a ]pyrimidines Induce a Strong Antiproliferative Effect against Oral Cancer Cells. Organometallics. [DOI: 10.1021/acs.organomet.2c00348] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Binici A, Elmas G, Okumuş A, Güzel R, Şimşek H, Kılıç Z. Phosphorus–nitrogen compounds: Part 60: Synthesis of hexaminomonoferrocenyl-spiro(N/O)cyclotetraphosphazenes: Spectral and electrochemical properties, tuning of redox feature, and antituberculosis activity. Phosphorus, Sulfur, and Silicon and the Related Elements. [DOI: 10.1080/10426507.2022.2100888] [Reference Citation Analysis]
8 Hammoud MM, Khattab M, Abdel-Motaal M, Van der Eycken J, Alnajjar R, Abulkhair HS, Al-Karmalawy AA. Synthesis, structural characterization, DFT calculations, molecular docking, and molecular dynamics simulations of a novel ferrocene derivative to unravel its potential antitumor activity. J Biomol Struct Dyn 2022;:1-18. [PMID: 35674744 DOI: 10.1080/07391102.2022.2082533] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
9 Zhang L, Xie M. The crystal structure of ( E )-3-(2-chlorophenyl)-1-ferrocenylprop-2-en-1-one, C 19 H 15 ClFeO. Zeitschrift für Kristallographie - New Crystal Structures 2022;0. [DOI: 10.1515/ncrs-2022-0042] [Reference Citation Analysis]
10 Zhang J, Huang X. The crystal structure of (2 E ,4 E )-1-ferrocenyl-5-phenylpenta-2,4-dien-1-one, C 21 H 18 FeO. Zeitschrift für Kristallographie - New Crystal Structures 2022;0. [DOI: 10.1515/ncrs-2022-0048] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
11 Shuvalov VY, Rozhkova YS, Plekhanova IV, Kostyuchenko AS, Shklyaev YV, Fisyuk AS. Synthesis of 3-Amino-6,7-Dihydroferroceno[a]Quinolizin-4-One Derivatives via the Reaction of 3,4-Dihydroferroceno[c]Pyridines with Azlactones. Chem Heterocycl Comp. [DOI: 10.1007/s10593-022-03050-5] [Reference Citation Analysis]
12 Li D, Gao S, Ye K, Wang Q, Xie C, Wu W, Feng L, Jiang L, Zheng K, Pang Q. Membrane-active La(III) and Ce(III) complexes as potent antibacterial agents: synthesis, characterization, in vitro, in silico, and in vivo studies. Journal of Molecular Structure 2022;1249:131595. [DOI: 10.1016/j.molstruc.2021.131595] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
13 Huang M, Kong J, Zhang J, Wang Z, Hao D, Zhang J, Wang Y, Qi W, Su R, He Z. Enhanced Polychromatic Luminescence of Bionic Peptidyl Nanoparticles Driven by Hydrogen Bonds. Part & Part Syst Charact. [DOI: 10.1002/ppsc.202100260] [Reference Citation Analysis]
14 Ramalakshmi S, Sonanki K, Prakash R, Usha G, Karpagalakshmi K, Nagarajan E, Selvapalam N. In–silico approach of effect of protein on complexation of cucurbit[7]uril with N- (ferrocenylmethyl) aniline. Materials Today: Proceedings 2022;51:1733-7. [DOI: 10.1016/j.matpr.2020.11.720] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Zhang R, Liu J, Zhu Z, Chen S, Wang F, Zhang J. Synthesis, Structure and Characterization of Two Ferrocene Functionalized Cadmium Metal Organic Frameworks . Acta Chimica Sinica 2022;80:249. [DOI: 10.6023/a21120611] [Reference Citation Analysis]
16 Wang QX, Guo ZC, Qin Y, Wang X, Li G. High Proton Conduction in Three Highly Water-Stable Hydrogen-Bonded Ferrocene-Based Phenyl Carboxylate Frameworks. Inorg Chem 2021;60:19278-86. [PMID: 34860499 DOI: 10.1021/acs.inorgchem.1c03093] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
17 Chaudhary A, Poonia K. The redox mechanism of ferrocene and its phytochemical and biochemical compounds in anticancer therapy: A mini review. Inorganic Chemistry Communications 2021;134:109044. [DOI: 10.1016/j.inoche.2021.109044] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
18 Wieczorek-Błauż A, Kowalczyk K, Błauż A, Makal A, Pawlędzio S, Eurtivong C, Arabshahi HJ, Reynisson J, Hartinger CG, Rychlik B, Plażuk D. Impact of the ferrocenyl group on cytotoxicity and KSP inhibitory activity of ferrocenyl monastrol conjugates. Dalton Trans 2021. [PMID: 34787141 DOI: 10.1039/d1dt03553c] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
19 Schlagintweit JF, Jakob CHG, Wilke NL, Ahrweiler M, Frias C, Frias J, König M, Esslinger EHJ, Marques F, Machado JF, Reich RM, Morais TS, Correia JDG, Prokop A, Kühn FE. Gold(I) Bis(1,2,3-triazol-5-ylidene) Complexes as Promising Selective Anticancer Compounds. J Med Chem 2021;64:15747-57. [PMID: 34670090 DOI: 10.1021/acs.jmedchem.1c01021] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
20 Asfiya R, Maiti B, Kamra M, Karande AA, Bhattacharya S. Novel α-tocopherol-ferrocene conjugates for the specific delivery of transgenes in liver cancer cells under high serum conditions. Biomater Sci 2021;9:7636-47. [PMID: 34676384 DOI: 10.1039/d1bm00607j] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
21 Kavitha N, Thamilarasan V, Sengottuvelan N. Diketonato based ferrocene appended cyclometalated iridium(III) complexes: Anti-microbial and anti-cancer studies. Journal of Organometallic Chemistry 2021;952:122032. [DOI: 10.1016/j.jorganchem.2021.122032] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
22 Su W, Fu T, Xu Z. Bis(ethanol-κ O )bis(1-ferrocenyl-4,4,4-trifluorobutane-1,3-dionato-κ 2O , O ′)nickel(II). IUCrData 2021;6. [DOI: 10.1107/s2414314621006933] [Reference Citation Analysis]
23 Yeo CI, Tiekink ERT, Chew J. Insights into the Antimicrobial Potential of Dithiocarbamate Anions and Metal-Based Species. Inorganics 2021;9:48. [DOI: 10.3390/inorganics9060048] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
24 Ludwig BS, Tomassi S, Di Maro S, Di Leva FS, Benge A, Reichart F, Nieberler M, Kühn FE, Kessler H, Marinelli L, Reuning U, Kossatz S. The organometallic ferrocene exhibits amplified anti-tumor activity by targeted delivery via highly selective ligands to αvβ3, αvβ6, or α5β1 integrins. Biomaterials 2021;271:120754. [PMID: 33756215 DOI: 10.1016/j.biomaterials.2021.120754] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
25 Huang Z, Yu H, Wang L, Liu X, Lin T, Haq F, Vatsadze SZ, Lemenovskiy DA. Ferrocene-contained metal organic frameworks: From synthesis to applications. Coordination Chemistry Reviews 2021;430:213737. [DOI: 10.1016/j.ccr.2020.213737] [Cited by in Crossref: 5] [Cited by in F6Publishing: 31] [Article Influence: 5.0] [Reference Citation Analysis]
26 Toro PM, Oyarzo J, Arancibia R, Wilkinson S, Artigas V, Fuentealba M, Moncada-basualto M, Olea-azar C, Vega A, Hugo Klahn A. Comparison of chemical and biological properties of organometallic complexes containing 4- and 5-nitrothienyl groups. Polyhedron 2021;193:114872. [DOI: 10.1016/j.poly.2020.114872] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
27 Román T, Ramirez D, Fierro-medina R, Santillan R, Farfán N. Ferrocene and Organotin (IV) Conjugates Containing Amino Acids and Peptides: A Promising Strategy for Searching New Therapeutic and Diagnostic Tools. COC 2020;24:2426-47. [DOI: 10.2174/1385272824999201001154259] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
28 González‐pelayo S, Bernardo O, Borge J, López LA. Synthesis of Metallocene Analogues of the Phenethylamine and Tetrahydroisoquinoline Scaffolds via Regioselective Ring Opening of 2‐Aryl‐ N ‐sulfonyl Aziridines. Adv Synth Catal 2021;363:819-25. [DOI: 10.1002/adsc.202001210] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
29 Keszei SJ, Pekker P, Fehér C, Balogh S, Jakab M, Nagy L, Skoda-földes R. Application of sol-gel methods to obtain silica materials decorated with ferrocenyl-ureidopyrimidine moieties. Preparation of hollow spheres and modification of a carbon electrode. Microporous and Mesoporous Materials 2020;308:110380. [DOI: 10.1016/j.micromeso.2020.110380] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
30 Toma M, Kuvek T, Vrček V. Ionization Energy and Reduction Potential in Ferrocene Derivatives: Comparison of Hybrid and Pure DFT Functionals. J Phys Chem A 2020;124:8029-39. [PMID: 32900203 DOI: 10.1021/acs.jpca.0c06663] [Cited by in Crossref: 3] [Cited by in F6Publishing: 7] [Article Influence: 1.5] [Reference Citation Analysis]
31 Efimov NN, Loginov DA, Sharipov MY, Nazarov AA, Nelyubina YV, Perekalin DS. Unexpected antifungal activity of half-sandwich complexes with metal−iodine bonds. Journal of Organometallic Chemistry 2020;916:121272. [DOI: 10.1016/j.jorganchem.2020.121272] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
32 Rahimpour K, Shafagh‐azar A, Abbasi H, Mohammad‐gholizadeh A, Hezarkhani Z, Teimuri‐mofrad R. 2‐[(4‐Aminobutyl)ferrocenylmethylidene]‐5,6‐dimethoxy‐1‐indanone derivatives: Synthesis, characterization, and investigation of electro‐optical properties. Appl Organometal Chem 2020;34. [DOI: 10.1002/aoc.5633] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
33 Taner B, Sevgi F, Göver T. Synthesis and Anti-Biofilm Activity of New Ferrocene Schiff Bases. Russ J Gen Chem 2020;90:907-10. [DOI: 10.1134/s1070363220050254] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
34 Wang R, Chen H, Yan W, Zheng M, Zhang T, Zhang Y. Ferrocene-containing hybrids as potential anticancer agents: Current developments, mechanisms of action and structure-activity relationships. Eur J Med Chem 2020;190:112109. [PMID: 32032851 DOI: 10.1016/j.ejmech.2020.112109] [Cited by in Crossref: 27] [Cited by in F6Publishing: 52] [Article Influence: 13.5] [Reference Citation Analysis]
35 Xiao J, Sun Z, Kong F, Gao F. Current scenario of ferrocene-containing hybrids for antimalarial activity. Eur J Med Chem 2020;185:111791. [PMID: 31669852 DOI: 10.1016/j.ejmech.2019.111791] [Cited by in Crossref: 23] [Cited by in F6Publishing: 31] [Article Influence: 7.7] [Reference Citation Analysis]