Jayadevan Jayashankaran

532 total citations
32 papers, 460 citations indexed

About

Jayadevan Jayashankaran is a scholar working on Organic Chemistry, Pharmacology and Pharmaceutical Science. According to data from OpenAlex, Jayadevan Jayashankaran has authored 32 papers receiving a total of 460 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Organic Chemistry, 11 papers in Pharmacology and 5 papers in Pharmaceutical Science. Recurrent topics in Jayadevan Jayashankaran's work include Synthesis of Organic Compounds (10 papers), Multicomponent Synthesis of Heterocycles (7 papers) and Oxidative Organic Chemistry Reactions (5 papers). Jayadevan Jayashankaran is often cited by papers focused on Synthesis of Organic Compounds (10 papers), Multicomponent Synthesis of Heterocycles (7 papers) and Oxidative Organic Chemistry Reactions (5 papers). Jayadevan Jayashankaran collaborates with scholars based in India, France and United States. Jayadevan Jayashankaran's co-authors include R. Raghunathan, S. Manian, Annie−Claude Gaumont, Jean‐François Lohier, Stéphane Perrio, Fabien Gelat, Natarajan Arumugam, Ramesh Rasappan, Asit R. Sarkar and Govindaswamy Manickam and has published in prestigious journals such as Tetrahedron, Organic Letters and Tetrahedron Letters.

In The Last Decade

Jayadevan Jayashankaran

32 papers receiving 451 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jayadevan Jayashankaran India 11 436 82 62 21 19 32 460
Atish Chandra India 11 361 0.8× 61 0.7× 71 1.1× 10 0.5× 27 1.4× 20 387
Shugao Zhu China 12 438 1.0× 31 0.4× 110 1.8× 31 1.5× 19 1.0× 24 485
Leonardo Moro Italy 9 495 1.1× 31 0.4× 48 0.8× 24 1.1× 30 1.6× 12 504
R. Raghunathan India 12 429 1.0× 94 1.1× 89 1.4× 27 1.3× 13 0.7× 46 441
Wangyang Tu China 8 375 0.9× 33 0.4× 58 0.9× 9 0.4× 23 1.2× 16 421
Madhukar S. Chande India 7 378 0.9× 39 0.5× 58 0.9× 14 0.7× 21 1.1× 39 402
Andrea Modi Germany 4 529 1.2× 80 1.0× 125 2.0× 21 1.0× 27 1.4× 7 554
Man‐Su Tu China 15 665 1.5× 45 0.5× 68 1.1× 48 2.3× 33 1.7× 32 674
Pradipta K. Basu India 10 399 0.9× 50 0.6× 40 0.6× 11 0.5× 16 0.8× 25 428
Manisha Swain India 12 411 0.9× 44 0.5× 64 1.0× 16 0.8× 51 2.7× 17 437

Countries citing papers authored by Jayadevan Jayashankaran

Since Specialization
Citations

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

Fields of papers citing papers by Jayadevan Jayashankaran

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jayadevan Jayashankaran

This figure shows the co-authorship network connecting the top 25 collaborators of Jayadevan Jayashankaran. A scholar is included among the top collaborators of Jayadevan Jayashankaran 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 Jayadevan Jayashankaran. Jayadevan Jayashankaran 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.
Xiao, Yufang, Srinivasa Karra, Andreas Goutopoulos, et al.. (2019). Synthesis and SAR development of quinoline analogs as novel P2X7 receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 29(13). 1660–1664. 9 indexed citations
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Jayashankaran, Jayadevan, et al.. (2013). A Facile One‐Pot Synthesis of Pyrrolo[1, 2‐a] Indoles by Intramolecular1,3‐Dipolar Cycloaddition under Neat‐Microwave Irradiation. Journal of Heterocyclic Chemistry. 50(2). 442–449. 7 indexed citations
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Manian, S., Jayadevan Jayashankaran, & R. Raghunathan. (2007). Indium trichloride catalyzed one-pot synthesis of indolo[2,1-a]pyrrolo[4′,3′:2,3]-7a,8,13,13b-tetrahydroquinolines through intramolecular imino Diels–Alder reactions. Tetrahedron Letters. 48(23). 4139–4142. 10 indexed citations
7.
Manian, S., Jayadevan Jayashankaran, Ramesh Rasappan, & R. Raghunathan. (2006). Rapid synthesis of tetrahydroquinolines by indium trichloride catalyzed mono- and bis-intramolecular imino Diels–Alder reactions. Tetrahedron Letters. 47(43). 7571–7574. 24 indexed citations
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Manian, S., Jayadevan Jayashankaran, & R. Raghunathan. (2006). Microwave induced one-pot synthesis of fluorenespiro[9.3′]-(4′-aryl)pyrrolidine/pyrrolizidine/tetrahydropyrrolo[1,2-c]thiazolespiro[2′.2″]indan-1″,3″-dione derivatives. Tetrahedron. 62(52). 12357–12362. 18 indexed citations
10.
Jayashankaran, Jayadevan, S. Manian, & R. Raghunathan. (2006). An efficient synthesis of thiopyrano[5,6-c]coumarin/[6,5-c]chromones through intramolecular domino Knoevenagel hetero Diels–Alder reactions. Tetrahedron Letters. 47(13). 2265–2270. 38 indexed citations
11.
Manian, S., Jayadevan Jayashankaran, & R. Raghunathan. (2006). A rapid access to indolo[2,1-a]pyrrolo[4′,3′:4,5]pyrano[5,6-c]coumarin/[6,5-c]chromone derivatives by domino Knoevenagal intramolecular hetero Diels–Alder reactions. Tetrahedron Letters. 48(8). 1385–1389. 36 indexed citations
12.
Jayashankaran, Jayadevan, et al.. (2005). 連続的に分子内1,3‐双極環状付加及びPictet‐Spengler環化を経るベンゾ‐/ナフト‐ピラノ‐インドリジノ‐インドールへの容易な経路. Synlett. 1167–1169. 1 indexed citations
13.
Arumugam, Natarajan, Jayadevan Jayashankaran, S. Manian, & R. Raghunathan. (2005). A novel access to highly functionalised β-lactams by regio- and stereoselective 1,3-dipolar cycloaddition reaction. Tetrahedron. 61(35). 8512–8516. 30 indexed citations
14.
Jayashankaran, Jayadevan, et al.. (2005). Novel Synthesis of N‐Methyl Spiropyrrolidines by 1,3‐Dipolar Cycloaddition Reaction of Azomethine Ylides. Synthetic Communications. 35(16). 2189–2193. 4 indexed citations
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Aravindan, P.G., S. Selvanayagam, D. Velmurugan, et al.. (2004). 1′-Methyl-4′-phenyl-H-fluorene-9-spiro-3′-pyrrolidine-2′-spiro-3′′-1H-indol-2′'(3′′H)-one. Acta Crystallographica Section E Structure Reports Online. 60(11). o2152–o2154. 1 indexed citations
17.
Jayashankaran, Jayadevan, S. Manian, & R. Raghunathan. (2004). A facile synthesis of novel dispiroheterocycles through solvent-free microwave-assisted [3+2] cycloaddition of azomethine ylides. Tetrahedron Letters. 45(39). 7303–7305. 52 indexed citations
18.
Jayashankaran, Jayadevan, et al.. (2003). A Novel Entry into a New Class of Dispiroheterocycles Through Azomethine Ylides Involving Unusual Dipolarophiles. Synthetic Communications. 33(3). 499–506. 2 indexed citations
19.
Manian, S., Jayadevan Jayashankaran, & R. Raghunathan. (2003). A New Access to Dispiro 7-Oxaindazolidines Spiroxindole Derivatives. Synthetic Communications. 33(23). 4053–4061. 6 indexed citations
20.
Jayashankaran, Jayadevan, et al.. (2003). An Easy Access to Spiroisoxazoline [5,31] Flavan-41-one Through 1,3-Dipolar Cycloaddition Reaction of Nitrile Oxide to Unusual Dipolarophiles. Synthetic Communications. 33(23). 4063–4069. 9 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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