Srinivasan Easwar

616 total citations
30 papers, 466 citations indexed

About

Srinivasan Easwar is a scholar working on Organic Chemistry, Molecular Biology and Catalysis. According to data from OpenAlex, Srinivasan Easwar has authored 30 papers receiving a total of 466 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Organic Chemistry, 12 papers in Molecular Biology and 4 papers in Catalysis. Recurrent topics in Srinivasan Easwar's work include Asymmetric Synthesis and Catalysis (18 papers), Synthesis and Catalytic Reactions (7 papers) and Chemical Synthesis and Analysis (6 papers). Srinivasan Easwar is often cited by papers focused on Asymmetric Synthesis and Catalysis (18 papers), Synthesis and Catalytic Reactions (7 papers) and Chemical Synthesis and Analysis (6 papers). Srinivasan Easwar collaborates with scholars based in India, Italy and Russia. Srinivasan Easwar's co-authors include Claudio Trombini, Filippo Pasi, Marco Lombardo, Narshinha P. Argade, Dilip D. Dhavale, Alessandro De Marco, Vedavati G. Puranik, Krishna N. Ganesh, Alexander S. Kucherenko and Sergei G. Zlotin and has published in prestigious journals such as Chemical Communications, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Srinivasan Easwar

25 papers receiving 458 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Srinivasan Easwar India 11 413 146 110 88 33 30 466
Filippo Pasi Italy 10 390 0.9× 152 1.0× 108 1.0× 92 1.0× 29 0.9× 13 438
Zhaoqin Jiang China 9 798 1.9× 40 0.3× 176 1.6× 165 1.9× 31 0.9× 11 838
S. A. Siddiqui India 8 671 1.6× 115 0.8× 135 1.2× 33 0.4× 26 0.8× 13 728
Esa T. T. Kumpulainen Finland 8 312 0.8× 24 0.2× 76 0.7× 103 1.2× 21 0.6× 12 361
Fabiano Kauer Zinn Brazil 9 691 1.7× 96 0.7× 75 0.7× 203 2.3× 51 1.5× 12 776
Zhongqiang Zhou China 14 381 0.9× 33 0.2× 69 0.6× 104 1.2× 73 2.2× 48 472
Rana Chatterjee India 15 585 1.4× 40 0.3× 84 0.8× 43 0.5× 18 0.5× 64 630
Kasiviswanadharaju Pericherla India 19 897 2.2× 29 0.2× 123 1.1× 47 0.5× 16 0.5× 26 941
Angelika S. Magnus Sweden 5 302 0.7× 23 0.2× 73 0.7× 65 0.7× 15 0.5× 5 344

Countries citing papers authored by Srinivasan Easwar

Since Specialization
Citations

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

Fields of papers citing papers by Srinivasan Easwar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Srinivasan Easwar

This figure shows the co-authorship network connecting the top 25 collaborators of Srinivasan Easwar. A scholar is included among the top collaborators of Srinivasan Easwar 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 Srinivasan Easwar. Srinivasan Easwar 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.
Easwar, Srinivasan, et al.. (2025). Access to isolable cyclic dienamines and N-aryl-2-aminobenzophenones from Morita–Baylis–Hillman ketones. New Journal of Chemistry. 49(11). 4639–4646.
2.
Easwar, Srinivasan, et al.. (2024). A retro-Mannich mediated transformation of Morita–Baylis–Hillman ketones to saturated imidazo[1,2-a]pyridines. Organic Chemistry Frontiers. 11(11). 3137–3150. 2 indexed citations
3.
Easwar, Srinivasan, et al.. (2024). Mechanistic Investigations on the Interaction of Morita–Baylis–Hillman Ketones with 2-Aminothiophenol. The Journal of Organic Chemistry. 89(10). 7263–7269.
4.
Reddy, S. Rajagopala, et al.. (2023). Acyl Transfer-Driven Rauhut–Currier Dimerization of Morita–Baylis–Hillman Ketones. The Journal of Organic Chemistry. 88(4). 2023–2033. 7 indexed citations
5.
Reddy, S. Rajagopala, et al.. (2023). Cooperative assistance of a sulfonamide in a proline-mediated direct asymmetric aldol addition. New Journal of Chemistry. 47(36). 17042–17050. 2 indexed citations
6.
Easwar, Srinivasan, et al.. (2022). Synthesis of 2,2-Disubstituted Dihydro-1,4-benzothiazines from Morita–Baylis–Hillman Ketones by an Oxidative Cyclization. The Journal of Organic Chemistry. 87(9). 5760–5772. 7 indexed citations
7.
Easwar, Srinivasan, et al.. (2020). Diamine-mediated degradative dimerisation of Morita–Baylis–Hillman ketones. Chemical Communications. 56(19). 2949–2952. 7 indexed citations
8.
Easwar, Srinivasan, et al.. (2019). A Hydrazine Insertion Route to N′-Alkyl Benzohydrazides by an Unexpected Carbon–Carbon Bond Cleavage. Organic Letters. 21(20). 8191–8195. 14 indexed citations
9.
Easwar, Srinivasan, et al.. (2018). An expedient access to chromanols via an arginine-mediated cascade cyclisation in water. Tetrahedron Letters. 59(24). 2356–2359. 1 indexed citations
10.
Easwar, Srinivasan, et al.. (2017). An Arginine‐Mediated Protocol for the Aldol Addition of Methyl Vinyl Ketone in Water. ChemistrySelect. 2(35). 11666–11672. 3 indexed citations
11.
Easwar, Srinivasan, et al.. (2016). Proline-Mediated Baylis–Hillman Reaction of Methyl Vinyl Ketone without a Co-catalyst under Solvent-Free Conditions. Synlett. 28(1). 128–132. 10 indexed citations
12.
Argade, Narshinha P., et al.. (2009). Synthesis of the Reported Protoberberine Gusanlung D. Synthesis. 2009(10). 1667–1672. 7 indexed citations
13.
Lombardo, Marco, Srinivasan Easwar, Filippo Pasi, & Claudio Trombini. (2009). The Ion Tag Strategy as a Route to Highly Efficient Organocatalysts for the Direct Asymmetric Aldol Reaction. Advanced Synthesis & Catalysis. 351(1-2). 276–282. 87 indexed citations
14.
Lombardo, Marco, Srinivasan Easwar, Alessandro De Marco, Filippo Pasi, & Claudio Trombini. (2008). A modular approach to catalyst hydrophobicity for an asymmetric aldol reaction in a biphasic aqueous environment. Organic & Biomolecular Chemistry. 6(22). 4224–4224. 35 indexed citations
15.
Lombardo, Marco, Srinivasan Easwar, Filippo Pasi, Claudio Trombini, & Dilip D. Dhavale. (2008). Protonated arginine and lysine as catalysts for the direct asymmetric aldol reaction in ionic liquids. Tetrahedron. 64(39). 9203–9207. 44 indexed citations
16.
Lombardo, Marco, Filippo Pasi, Srinivasan Easwar, & Claudio Trombini. (2007). An Improved Protocol for the Direct Asymmetric Aldol Reaction in Ionic Liquids, Catalysed by Onium Ion‐Tagged Prolines. Advanced Synthesis & Catalysis. 349(11-12). 2061–2065. 85 indexed citations
17.
Easwar, Srinivasan, et al.. (2007). Facile air-oxidation of N-homopiperonyl-5,6-dimethoxyhomophthalimide: simple and efficient access to nuevamine. Tetrahedron. 64(8). 1786–1791. 24 indexed citations
18.
Easwar, Srinivasan & Narshinha P. Argade. (2003). Amano PS Catalyzed Methanolysis of Maleimides: An Efficient Synthesis of Methyl Maleanilates.. ChemInform. 34(1). 1 indexed citations
19.
Easwar, Srinivasan & Narshinha P. Argade. (2002). Amano PS catalysed methanolysis of maleimides: An efficient synthesis of methyl maleanilates. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 41(9). 1899–1901. 1 indexed citations
20.
Easwar, Srinivasan, et al.. (2002). Enantioselective enzymatic approach to (+)- and (−)-2-acetoxy/hydroxycyclopentanones. Tetrahedron Asymmetry. 13(13). 1367–1371. 16 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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