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Cited by in F6Publishing
For: Kumar K, Carrère-kremer S, Kremer L, Guérardel Y, Biot C, Kumar V. Azide–alkynecycloadditionen route towards 1H-1,2,3-triazole-tethered β-lactam–ferrocene and β-lactam–ferrocenylchalcone conjugates: synthesis and in vitro anti-tubercular evaluation. Dalton Trans 2013;42:1492-500. [DOI: 10.1039/c2dt32148c] [Cited by in Crossref: 44] [Cited by in F6Publishing: 45] [Article Influence: 4.4] [Reference Citation Analysis]
Number Citing Articles
1 Desiatkina O, Mösching M, Anghel N, Boubaker G, Amdouni Y, Hemphill A, Furrer J, Păunescu E. New Nucleic Base-Tethered Trithiolato-Bridged Dinuclear Ruthenium(II)-Arene Compounds: Synthesis and Antiparasitic Activity. Molecules 2022;27. [PMID: 36500266 DOI: 10.3390/molecules27238173] [Reference Citation Analysis]
2 Al-rasheed HH, Al-majid AM, Ali M, Haukka M, Ramadan S, Soliman SM, El-faham A, Domingo LR, Barakat A. [3 + 2] Cycloadditions in Asymmetric Synthesis of Spirooxindole Hybrids Linked to Triazole and Ferrocene Units: X-ray Crystal Structure and MEDT Study of the Reaction Mechanism. Symmetry 2022;14:2071. [DOI: 10.3390/sym14102071] [Reference Citation Analysis]
3 Domingo LR, Ríos-Gutiérrez M, Barakat A. A Molecular Electron Density Theory Study of the [3+2] Cycloaddition Reaction of an Azomethine Ylide with an Electrophilic Ethylene Linked to Triazole and Ferrocene Units. Molecules 2022;27:6532. [PMID: 36235069 DOI: 10.3390/molecules27196532] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 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]
5 Altowyan MS, Soliman SM, Haukka M, Al-shaalan NH, Alkharboush AA, Barakat A. Synthesis and Structure Elucidation of Novel Spirooxindole Linked to Ferrocene and Triazole Systems via [3 + 2] Cycloaddition Reaction. Molecules 2022;27:4095. [DOI: 10.3390/molecules27134095] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
6 Sharma A, Agrahari AK, Rajkhowa S, Tiwari VK. Emerging impact of triazoles as anti-tubercular agent. Eur J Med Chem 2022;238:114454. [PMID: 35597009 DOI: 10.1016/j.ejmech.2022.114454] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Mbaba M, Khanye SD, Smith GS, Biot C. Organometallic Chemistry of Drugs Based on Iron. Comprehensive Organometallic Chemistry IV 2022. [DOI: 10.1016/b978-0-12-820206-7.00046-9] [Reference Citation Analysis]
8 Chang C, Lee G. Synthesis of ruthenium triazolato complexes by the [3 + 2] cycloaddition of a ruthenium azido complex with acetylacetylenes. Inorganica Chimica Acta 2019;494:232-8. [DOI: 10.1016/j.ica.2019.05.031] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 1.3] [Reference Citation Analysis]
9 Chang CW, Lee GH. Facile synthesis of 1,5-disubstituted 1,2,3-triazoles by the regiospecific alkylation of a ruthenium triazolato complex. Dalton Trans 2019;48:2028-37. [PMID: 30656320 DOI: 10.1039/c8dt04189j] [Cited by in Crossref: 6] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
10 Chang C, Lin Y, Lee G, Wang Y. [3+2] Cycloaddition of ruthenium azido complex with ethyl propiolate and related reactions. Journal of Organometallic Chemistry 2018;860:72-7. [DOI: 10.1016/j.jorganchem.2018.01.049] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 1.6] [Reference Citation Analysis]
11 Singh A, Saha ST, Perumal S, Kaur M, Kumar V. Azide-Alkyne Cycloaddition En Route to 1H-1,2,3-Triazole-Tethered Isatin-Ferrocene, Ferrocenylmethoxy-Isatin, and Isatin-Ferrocenylchalcone Conjugates: Synthesis and Antiproliferative Evaluation. ACS Omega 2018;3:1263-8. [PMID: 30023800 DOI: 10.1021/acsomega.7b01755] [Cited by in Crossref: 27] [Cited by in F6Publishing: 27] [Article Influence: 5.4] [Reference Citation Analysis]
12 Bhalla A, Bari SS, Bhalla J. Synthesis of Diverse β-Lactams: Role of Appended Hetero Moiety on Its Activity. Beta-Lactams 2017. [DOI: 10.1007/978-3-319-55621-5_1] [Reference Citation Analysis]
13 Bari SS, Bhalla A, Bhalla J. Role of Transition Metal Reagents in β-Lactam Synthesis: New Paradigms. Beta-Lactams 2017. [DOI: 10.1007/978-3-319-55621-5_2] [Reference Citation Analysis]
14 Zheng ZJ, Wang D, Xu Z, Xu LW. Synthesis of bi- and bis-1,2,3-triazoles by copper-catalyzed Huisgen cycloaddition: A family of valuable products by click chemistry. Beilstein J Org Chem 2015;11:2557-76. [PMID: 26734102 DOI: 10.3762/bjoc.11.276] [Cited by in Crossref: 58] [Cited by in F6Publishing: 59] [Article Influence: 7.3] [Reference Citation Analysis]
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