T. M. Rangarajan

852 total citations
44 papers, 632 citations indexed

About

T. M. Rangarajan is a scholar working on Organic Chemistry, Pharmacology and Pharmaceutical Science. According to data from OpenAlex, T. M. Rangarajan has authored 44 papers receiving a total of 632 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Organic Chemistry, 12 papers in Pharmacology and 8 papers in Pharmaceutical Science. Recurrent topics in T. M. Rangarajan's work include Cholinesterase and Neurodegenerative Diseases (12 papers), Synthesis and Biological Evaluation (9 papers) and Electrochemical sensors and biosensors (8 papers). T. M. Rangarajan is often cited by papers focused on Cholinesterase and Neurodegenerative Diseases (12 papers), Synthesis and Biological Evaluation (9 papers) and Electrochemical sensors and biosensors (8 papers). T. M. Rangarajan collaborates with scholars based in India, South Korea and Saudi Arabia. T. M. Rangarajan's co-authors include Bijo Mathew, Rishi Pal Singh, Hoon Kim, Sunil Kumar, Aathira Sujathan Nair, Ashok K. Prasad, V. Baliah, Rabindra Prasad Singh, Rajendra Singh and Ashutosh Kumar Singh and has published in prestigious journals such as Scientific Reports, Coordination Chemistry Reviews and The Journal of Organic Chemistry.

In The Last Decade

T. M. Rangarajan

43 papers receiving 623 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
T. M. Rangarajan India 14 411 139 128 118 77 44 632
Aathira Sujathan Nair India 10 171 0.4× 93 0.7× 70 0.5× 79 0.7× 57 0.7× 15 329
Mevlüt Ertan Türkiye 17 930 2.3× 105 0.8× 53 0.4× 217 1.8× 33 0.4× 44 1.2k
Erika M. Milczek United States 11 536 1.3× 85 0.6× 18 0.1× 242 2.1× 34 0.4× 12 812
Mohamed Abarbri France 21 1.3k 3.2× 85 0.6× 115 0.9× 172 1.5× 14 0.2× 104 1.5k
Pilar López‐Alvarado Spain 18 732 1.8× 105 0.8× 20 0.2× 247 2.1× 43 0.6× 53 976
Paul B. Huleatt Singapore 14 281 0.7× 104 0.7× 15 0.1× 108 0.9× 51 0.7× 17 508
Hena Khanam India 14 623 1.5× 107 0.8× 21 0.2× 164 1.4× 62 0.8× 23 973
Morshed Alam Chowdhury Canada 18 624 1.5× 348 2.5× 111 0.9× 140 1.2× 37 0.5× 39 898
Vincent Gembus France 14 426 1.0× 138 1.0× 68 0.5× 175 1.5× 94 1.2× 32 582
Rafael P. Vieira Brazil 15 121 0.3× 52 0.4× 41 0.3× 109 0.9× 57 0.7× 31 484

Countries citing papers authored by T. M. Rangarajan

Since Specialization
Citations

This map shows the geographic impact of T. M. Rangarajan'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 T. M. Rangarajan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. M. Rangarajan more than expected).

Fields of papers citing papers by T. M. Rangarajan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by T. M. Rangarajan. 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 T. M. Rangarajan. The network helps show where T. M. Rangarajan may publish in the future.

Co-authorship network of co-authors of T. M. Rangarajan

This figure shows the co-authorship network connecting the top 25 collaborators of T. M. Rangarajan. A scholar is included among the top collaborators of T. M. Rangarajan 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 T. M. Rangarajan. T. M. Rangarajan 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
1.
Rangarajan, T. M., et al.. (2025). Deep Eutectic Solvents (DESs): Emerging viable solvent systems for transition-metal-catalyzed cross-coupling reactions. Journal of Molecular Liquids. 426. 127287–127287. 3 indexed citations
2.
Yadav, S. K., et al.. (2025). Greener media for nano catalysts in Suzuki Miyaura reaction. Coordination Chemistry Reviews. 528. 216431–216431. 5 indexed citations
3.
Rangarajan, T. M., et al.. (2024). Optimal exploitation of supported heterogenized Pd nanoparticles for C-C cross-coupling reactions. Coordination Chemistry Reviews. 507. 215763–215763. 21 indexed citations
4.
Yasin, Haya, Ankita Patel, Della Grace Thomas Parambi, et al.. (2024). Recent Progress in Synthetic and Natural Catechol-O-methyltransferase Inhibitors for Neurological Disorders. ACS Omega. 9(44). 44005–44018. 2 indexed citations
5.
Rangarajan, T. M., et al.. (2023). Solid-Supported Heterogenized Palladium Nanoparticles: Propitious Vehicles for Sonogashira Cross-Coupling Reaction. SynOpen. 7(1). 43–45. 4 indexed citations
6.
Kumar, Sunil, et al.. (2023). A Comprehensive Review of the Docking Studies of Chalcone for theDevelopment of Selective MAO-B Inhibitors. CNS & Neurological Disorders - Drug Targets. 23(6). 697–714. 3 indexed citations
7.
Rangarajan, T. M., et al.. (2023). Langlois Reagent: An Efficient Trifluoromethylation Reagent. SynOpen. 7(1). 65–68. 1 indexed citations
8.
Rangarajan, T. M., Sunil Kumar, Neelima Kukreti, et al.. (2023). “Click Chemistry”: An Emerging Tool for Developing a New Class of Structural Motifs against Various Neurodegenerative Disorders. ACS Omega. 8(47). 44437–44457. 14 indexed citations
9.
Mathew, Bijo, Ravichandran Veerasamy, T. M. Rangarajan, et al.. (2022). Two dimensional-QSAR and molecular dynamics studies of a selected class of aldoxime- and hydroxy-functionalized chalcones as monoamine oxidase-B inhibitors. Journal of Biomolecular Structure and Dynamics. 41(19). 9256–9266. 15 indexed citations
10.
Rangarajan, T. M., et al.. (2022). Revealing the role of the benzyloxy pharmacophore in the design of a new class of monoamine oxidase‐B inhibitors. Archiv der Pharmazie. 355(8). e2200084–e2200084. 21 indexed citations
11.
Mathew, Bijo, Jong‐Min Oh, Ahmed Khames, et al.. (2021). Replacement of Chalcone-Ethers with Chalcone-Thioethers as Potent and Highly Selective Monoamine Oxidase-B Inhibitors and Their Protein-Ligand Interactions. Pharmaceuticals. 14(11). 1148–1148. 10 indexed citations
12.
Rangarajan, T. M., et al.. (2020). An Easy Access to Oxime Ethers byPd‐CatalyzedC—OCross‐Couplingof Activated Aryl Bromides with Ketoximes and Chalcone Oximes. Chinese Journal of Chemistry. 38(8). 830–836. 7 indexed citations
14.
Rangarajan, T. M., et al.. (2016). A general and efficient Pd-catalyzed rapid 2-fluoroethoxylation of bromo-chalcones. Journal of Fluorine Chemistry. 186. 101–110. 7 indexed citations
16.
Rangarajan, T. M., Rajendra Singh, Rajendra Singh, et al.. (2014). BrettPhos Ligand Supported Palladium‐Catalyzed CO Bond Formation through an Electronic Pathway of Reductive Elimination: Fluoroalkoxylation of Activated Aryl Halides. Chemistry - A European Journal. 20(44). 14218–14225. 65 indexed citations
18.
Ahmed, Fahim, et al.. (1975). THE SYNTHESIS OF BENZ[α]ANTHRACENE. Organic Preparations and Procedures International. 7(6). 267–270. 2 indexed citations
19.
Baliah, V. & T. M. Rangarajan. (1961). Notes. Synthesis of 3,5-Diaryl-1,4-thiasine 1,1-Dioxides.. The Journal of Organic Chemistry. 26(3). 970–971. 8 indexed citations
20.
Baliah, V. & T. M. Rangarajan. (1959). Possible intramolecular proton transfer during the electronic excitation of acetanilide. Die Naturwissenschaften. 46(3). 107–107. 5 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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