Reza Ranjbar‐Karimi

839 total citations
76 papers, 680 citations indexed

About

Reza Ranjbar‐Karimi is a scholar working on Organic Chemistry, Pharmaceutical Science and Pharmacology. According to data from OpenAlex, Reza Ranjbar‐Karimi has authored 76 papers receiving a total of 680 indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Organic Chemistry, 21 papers in Pharmaceutical Science and 7 papers in Pharmacology. Recurrent topics in Reza Ranjbar‐Karimi's work include Multicomponent Synthesis of Heterocycles (24 papers), Fluorine in Organic Chemistry (21 papers) and Synthesis and Biological Evaluation (20 papers). Reza Ranjbar‐Karimi is often cited by papers focused on Multicomponent Synthesis of Heterocycles (24 papers), Fluorine in Organic Chemistry (21 papers) and Synthesis and Biological Evaluation (20 papers). Reza Ranjbar‐Karimi collaborates with scholars based in Iran, India and United Kingdom. Reza Ranjbar‐Karimi's co-authors include Hossein Mehrabi, Alireza Bazmandegan‐Shamili, Mohammad Abdollahi‐Alibeik, Alireza Aslani, Majid Azizi, Hamzeh Izadi, Francesco Baino, Mojde Moradi Pour, Mohadeseh Hassanisaadi and Abbas Rahdar and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Chemical Physics Letters.

In The Last Decade

Reza Ranjbar‐Karimi

76 papers receiving 663 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Reza Ranjbar‐Karimi Iran 13 435 125 95 93 77 76 680
Zhiguo Zheng China 10 409 0.9× 76 0.6× 50 0.5× 160 1.7× 85 1.1× 28 699
Hongjun Zhu China 15 144 0.3× 73 0.6× 47 0.5× 185 2.0× 91 1.2× 25 576
Elmutasim O. Ibnouf Saudi Arabia 10 87 0.2× 68 0.5× 48 0.5× 65 0.7× 48 0.6× 21 373
Yangyang Ma China 13 325 0.7× 120 1.0× 47 0.5× 110 1.2× 106 1.4× 63 691
Xu Yan China 16 620 1.4× 23 0.2× 107 1.1× 63 0.7× 151 2.0× 38 886
Hongyan Si China 12 113 0.3× 29 0.2× 89 0.9× 46 0.5× 51 0.7× 27 381
Shikha Rani India 12 241 0.6× 32 0.3× 32 0.3× 57 0.6× 173 2.2× 26 488
Wen‐Xian Zhao China 19 920 2.1× 62 0.5× 142 1.5× 42 0.5× 153 2.0× 53 1.2k
Jiakun Su China 11 80 0.2× 56 0.4× 51 0.5× 67 0.7× 171 2.2× 23 537
Ibrar Hussain Germany 14 567 1.3× 41 0.3× 17 0.2× 106 1.1× 64 0.8× 38 770

Countries citing papers authored by Reza Ranjbar‐Karimi

Since Specialization
Citations

This map shows the geographic impact of Reza Ranjbar‐Karimi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Reza Ranjbar‐Karimi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Reza Ranjbar‐Karimi more than expected).

Fields of papers citing papers by Reza Ranjbar‐Karimi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Reza Ranjbar‐Karimi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Reza Ranjbar‐Karimi. The network helps show where Reza Ranjbar‐Karimi may publish in the future.

Co-authorship network of co-authors of Reza Ranjbar‐Karimi

This figure shows the co-authorship network connecting the top 25 collaborators of Reza Ranjbar‐Karimi. A scholar is included among the top collaborators of Reza Ranjbar‐Karimi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Reza Ranjbar‐Karimi. Reza Ranjbar‐Karimi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
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Ranjbar‐Karimi, Reza, et al.. (2024). Recent Advances in the Synthesis and Applications of Ionic Liquids Derived from Natural Products. Synthesis. 56(23). 3519–3542. 2 indexed citations
3.
Roostaee, Maryam & Reza Ranjbar‐Karimi. (2024). Emerging trends in carbon quantum dots: Synthesis, characterization, and environmental photodegradation applications. Materials Science in Semiconductor Processing. 188. 109212–109212. 10 indexed citations
4.
Darehkordi, Ali, et al.. (2023). 2,2,2-Trifluoro- N -(1-iminoethyl)- N ′ arylacetimidamides as key intermediate for synthesis of trifluoromethyl 1,2,4-triazoles. Synthetic Communications. 53(12). 920–931. 3 indexed citations
5.
Ranjbar‐Karimi, Reza, et al.. (2023). Synthesis of acyclic triarylmethane-based compounds containing perfluoropyridine subunits using 4,4′-(p-tolylmethylene)bis(2,6-dimethylphenol) as a flexible spacer. Journal of Molecular Structure. 1302. 137360–137360. 1 indexed citations
6.
Saeednia, Samira, et al.. (2023). CuFe2O4@SiO2-LMnCl: an efficient, highly recyclable magnetic nanoparticle for synergic catalyzing of tetrazoles. Journal of the Iranian Chemical Society. 20(7). 1569–1578. 2 indexed citations
7.
Ranjbar‐Karimi, Reza, et al.. (2023). Synthesis of novel triarylmethane derivatives containing a trichloropyrimidine moiety. Journal of the Iranian Chemical Society. 20(12). 2917–2922. 1 indexed citations
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Ranjbar‐Karimi, Reza, et al.. (2021). 3,3'-((Arylmethylene)bis(4-methoxy-3,1-phenylene)) dipyridine derivatives as convenient ligands for Suzuki–Miyaura chemo- and homoselective cross-coupling reactions. Journal of the Iranian Chemical Society. 19(4). 1143–1158. 5 indexed citations
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Abdollahi‐Alibeik, Mohammad, et al.. (2018). FSM-16-SO 3 H nanoparticles as a novel heterogeneous catalyst: preparation, characterization, and catalytic application in the synthesis of polyhydroquinolines. Main Group Metal Chemistry. 41(3-4). 91–101. 19 indexed citations
13.
Abdollahi‐Alibeik, Mohammad, et al.. (2018). Fe3O4@FSM-16-SO3H as a new magnetically recyclable nanostructured catalyst: synthesis, characterization and catalytic application for the synthesis of pyrano[2,3-c]pyrazoles. 8(4). 311–323. 2 indexed citations
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Ranjbar‐Karimi, Reza, et al.. (2015). Synthesis of some fluorinated thiazolopyridine from pentafluoropyridine and 4-phenylsulfonyl tetrafluoropyridine. Arabian Journal of Chemistry. 12(8). 2037–2043. 2 indexed citations
16.
Riseh, Roohallah Saberi, et al.. (2013). Biological control of take-all disease by isolates ofPseudomonas fluorescensand biosynthesis of silver nanoparticles by the culture supernatant ofPseudomonas fluorescensCHA0. Archives of Phytopathology and Plant Protection. 47(14). 1752–1763. 2 indexed citations
17.
Darehkordi, Ali, Mahin Ramezani, & Reza Ranjbar‐Karimi. (2013). Synthesis of New Gluco‐, Galacto‐, and Mannopyranosylthiazoles, Thiazolidinones, and Pyranosylthiazlidin‐4‐ones from Sugar Thiosemicarbazone Derivatives. Heteroatom Chemistry. 24(3). 200–207. 2 indexed citations
18.
Izadi, Hamzeh, et al.. (2011). Bioactivity of essential oil from Satureja hortensis (Laminaceae) against three stored-product insect species. AFRICAN JOURNAL OF BIOTECHNOLOGY. 10(34). 6620–6627. 35 indexed citations
19.
Ranjbar‐Karimi, Reza, et al.. (2010). Ultrasound promoted facile synthesis of some pentafluoropyridine derivatives at ambient conditions. Ultrasonics Sonochemistry. 18(1). 258–263. 13 indexed citations
20.
Ranjbar‐Karimi, Reza, et al.. (2010). Regiochemistry of nucleophilic substitution of 4-phenylsulfonyl tetrafluoropyridine with unequal bidentate nucleophiles. Journal of Fluorine Chemistry. 131(5). 587–591. 25 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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