Shubhankar Samanta

694 total citations
46 papers, 522 citations indexed

About

Shubhankar Samanta is a scholar working on Organic Chemistry, Molecular Biology and Materials Chemistry. According to data from OpenAlex, Shubhankar Samanta has authored 46 papers receiving a total of 522 indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Organic Chemistry, 6 papers in Molecular Biology and 4 papers in Materials Chemistry. Recurrent topics in Shubhankar Samanta's work include Catalytic C–H Functionalization Methods (22 papers), Synthesis and Characterization of Pyrroles (10 papers) and Catalytic Cross-Coupling Reactions (9 papers). Shubhankar Samanta is often cited by papers focused on Catalytic C–H Functionalization Methods (22 papers), Synthesis and Characterization of Pyrroles (10 papers) and Catalytic Cross-Coupling Reactions (9 papers). Shubhankar Samanta collaborates with scholars based in India, United States and South Korea. Shubhankar Samanta's co-authors include Jayanta K. Ray, Jayanta K. Ray, Arabinda Mandal, Suresh Kumar Mondal, Tapas Das, Indranil Chatterjee, Soumen Giri, Mohammed Ikbal, Akash Jana and Maidul Hossain and has published in prestigious journals such as Journal of Materials Chemistry A, The Journal of Organic Chemistry and Chemistry - A European Journal.

In The Last Decade

Shubhankar Samanta

43 papers receiving 514 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shubhankar Samanta India 15 484 62 42 27 23 46 522
Alexey А. Festa Russia 13 670 1.4× 65 1.0× 26 0.6× 42 1.6× 42 1.8× 46 721
Anugula Nagaraju India 15 631 1.3× 53 0.9× 47 1.1× 29 1.1× 13 0.6× 23 655
Narsaiah Chinthala India 11 436 0.9× 59 1.0× 42 1.0× 43 1.6× 15 0.7× 17 467
Vignesh Palani United States 12 517 1.1× 81 1.3× 29 0.7× 85 3.1× 29 1.3× 18 588
Yogesh G. Shelke India 12 311 0.6× 38 0.6× 43 1.0× 31 1.1× 19 0.8× 14 370
Teresa A. Palazzo United States 15 520 1.1× 117 1.9× 35 0.8× 58 2.1× 11 0.5× 23 612
Yu. V. Shklyaev Russia 10 479 1.0× 59 1.0× 25 0.6× 34 1.3× 19 0.8× 133 522
Priti Khedkar India 10 407 0.8× 135 2.2× 18 0.4× 16 0.6× 13 0.6× 14 436
Ram N. Ram India 15 466 1.0× 91 1.5× 23 0.5× 82 3.0× 37 1.6× 33 504

Countries citing papers authored by Shubhankar Samanta

Since Specialization
Citations

This map shows the geographic impact of Shubhankar Samanta'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 Shubhankar Samanta with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shubhankar Samanta more than expected).

Fields of papers citing papers by Shubhankar Samanta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shubhankar Samanta. 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 Shubhankar Samanta. The network helps show where Shubhankar Samanta may publish in the future.

Co-authorship network of co-authors of Shubhankar Samanta

This figure shows the co-authorship network connecting the top 25 collaborators of Shubhankar Samanta. A scholar is included among the top collaborators of Shubhankar Samanta 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 Shubhankar Samanta. Shubhankar Samanta 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.
Haldar, Pallab Kanti, Suman Pradhan, Dipak Kumar Hazra, et al.. (2025). Design, synthesis, and in vitro and in vivo biological evaluation of 2-amino-naphtho[2,3-b]thiophene-4,9-dione derivatives as potent anticancer agents. European Journal of Medicinal Chemistry. 296. 117728–117728.
2.
Giri, Soumen, et al.. (2025). Metal–organic frameworks: classifications, synthesis, structure–property–performance relationship, and techno-economic analysis of redox flow batteries. Journal of Materials Chemistry A. 13(25). 19193–19235. 3 indexed citations
3.
4.
Ikbal, Mohammed, et al.. (2024). Progress in Electrochemically Empowered C−O Bond Formation: Unveiling the Pathway of Efficient Green Synthesis. Chemistry - An Asian Journal. 19(11). e202400116–e202400116. 7 indexed citations
5.
6.
Samanta, Shubhankar, et al.. (2024). Synthesis of Polynuclear Aromatic Hydrocarbons by Palladium-catalyzed C-H BondFunctionalization. Current Organic Chemistry. 28(18). 1387–1403. 2 indexed citations
7.
Roy, S. R., et al.. (2023). DBU Promoted Deformylative/Dehalogenative Difunctionalization to Access β‐Bromovinyl Aldehydes Derived from Tetralones**. European Journal of Organic Chemistry. 26(41). 3 indexed citations
8.
Samanta, Shubhankar, et al.. (2023). Recent advances in the synthesis of chromenone fused pyrrolo[2,1-a]isoquinoline derivatives. New Journal of Chemistry. 47(48). 22246–22268. 6 indexed citations
9.
Samanta, Jayanta, Nayim Sepay, Chandan Pal, et al.. (2023). Urea‐Promoted Neat Synthesis of Fused Dihydroisoquinolines and Disubstituted Pyridines: A Mechanistic Observation with Molecular‐Sensing Studies. Chemistry - A European Journal. 30(13). e202303287–e202303287. 4 indexed citations
10.
11.
Samanta, Shubhankar, et al.. (2022). Transition metal-free advanced synthetic approaches for isoindolinones and their fused analogues. New Journal of Chemistry. 46(17). 7780–7830. 21 indexed citations
12.
Molla, Mijanur Rahaman, et al.. (2020). First Example of Copper(I) Catalyzed Decarboalkoxymethylation of Alkyl 2‐[1‐(Pyridin‐2‐yl)‐1H‐pyrrol‐2‐yl]acetates. European Journal of Organic Chemistry. 2020(18). 2754–2760. 3 indexed citations
13.
Ikbal, Mohammed, et al.. (2020). A solvent- and catalyst-free tandem reaction: synthesis, and photophysical and biological applications of isoindoloquinazolinones. New Journal of Chemistry. 44(11). 4324–4331. 11 indexed citations
14.
Mondal, Suresh Kumar, et al.. (2019). One-pot tandem cyclisation to pyrrolo[1,2-a][1,4]benzodiazepines: a modified approach to the Pictet–Spengler reaction. Organic & Biomolecular Chemistry. 17(18). 4652–4662. 15 indexed citations
15.
Jana, Akash, Akash Jana, Mohammed Ikbal, et al.. (2018). NaN 3 /NH 4 Cl‐Promoted Aza‐Cyclization: A Convenient Route for Bio‐Active Diverse Isoindolinone Derivatives. ChemistrySelect. 3(42). 11950–11956. 5 indexed citations
16.
Mondal, Suresh Kumar, et al.. (2014). Platinum(II)-Catalyzed Novel Synthesis of 3,4-Fused Furans. Synthetic Communications. 45(5). 625–634. 3 indexed citations
17.
Samanta, Shubhankar, et al.. (2010). Palladium-catalyzed one-pot Suzuki coupling followed by arylpalladium addition to aldehyde: a convenient route to fluoren-9-one derivatives. Tetrahedron Letters. 51(42). 5604–5608. 42 indexed citations
18.
19.
Chatterjee, Indranil, et al.. (2008). Novel and Rapid Palladium-Assisted 6π Electrocyclic Reaction Affording 9,10-Dihydrophenanthrene and Its Analogues. Organic Letters. 10(21). 4795–4797. 46 indexed citations
20.
Samanta, Shubhankar, et al.. (2008). Pd(0) catalyzed intramolecular Heck reaction: a versatile route for the synthesis of 2-aryl substituted 5-, 6-, and 7-membered O-containing heterocycles. Tetrahedron Letters. 49(50). 7153–7156. 15 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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