Y. Lingappa

548 total citations
30 papers, 434 citations indexed

About

Y. Lingappa is a scholar working on Organic Chemistry, Materials Chemistry and Analytical Chemistry. According to data from OpenAlex, Y. Lingappa has authored 30 papers receiving a total of 434 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Organic Chemistry, 7 papers in Materials Chemistry and 6 papers in Analytical Chemistry. Recurrent topics in Y. Lingappa's work include Multicomponent Synthesis of Heterocycles (9 papers), Synthesis and biological activity (6 papers) and Electrochemical Analysis and Applications (5 papers). Y. Lingappa is often cited by papers focused on Multicomponent Synthesis of Heterocycles (9 papers), Synthesis and biological activity (6 papers) and Electrochemical Analysis and Applications (5 papers). Y. Lingappa collaborates with scholars based in India, United States and France. Y. Lingappa's co-authors include Lingaiah Nagarapu, P. Prathap, Rajashaker Bantu, K.T. Ramakrishna Reddy, N. Revathi, R.W. Miles, G. Rajeshwar Reddy, Manojit Pal, K. Deepa and K. Hussain Reddy and has published in prestigious journals such as Green Chemistry, Tetrahedron Letters and European Journal of Medicinal Chemistry.

In The Last Decade

Y. Lingappa

29 papers receiving 414 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Y. Lingappa India 11 242 172 117 40 24 30 434
Shriya H. Wadumethrige United States 8 340 1.4× 215 1.3× 158 1.4× 21 0.5× 27 1.1× 12 498
Gülbin Kurtay Türkiye 13 176 0.7× 110 0.6× 129 1.1× 49 1.2× 25 1.0× 37 462
Thorben Pfeifer Germany 8 224 0.9× 240 1.4× 118 1.0× 34 0.8× 18 0.8× 8 541
Cahit Örek Türkiye 13 234 1.0× 68 0.4× 40 0.3× 62 1.6× 37 1.5× 29 391
Mahdieh Ghavidel Iran 4 238 1.0× 65 0.4× 24 0.2× 54 1.4× 34 1.4× 6 363
Kenneth A. Belmore United States 11 173 0.7× 57 0.3× 65 0.6× 27 0.7× 6 0.3× 18 294
Zhengfen Liu China 13 356 1.5× 93 0.5× 36 0.3× 38 0.9× 15 0.6× 28 479
M. N. Alberti Greece 16 293 1.2× 160 0.9× 52 0.4× 45 1.1× 67 2.8× 23 458
Bingchuan Yang China 13 316 1.3× 97 0.6× 38 0.3× 70 1.8× 18 0.8× 49 465
M. E. Niyazymbetov Russia 12 304 1.3× 76 0.4× 36 0.3× 40 1.0× 10 0.4× 45 361

Countries citing papers authored by Y. Lingappa

Since Specialization
Citations

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

Fields of papers citing papers by Y. Lingappa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Y. Lingappa

This figure shows the co-authorship network connecting the top 25 collaborators of Y. Lingappa. A scholar is included among the top collaborators of Y. Lingappa 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 Y. Lingappa. Y. Lingappa 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.
Deepa, K., et al.. (2015). A simple spectrophotometric method for the determination ofarsenic in industrial and environmental samples using vanillin-2-amino nicotinic acid (VANA). Der pharmacia lettre. 7(7). 345–352. 1 indexed citations
2.
Deepa, K., et al.. (2014). Spectrophotometric determination of lead in medicinal leaf and environmental samples using 5-methylthiophene–2-carboxaldehyde ethylenediamine (MTCED). Der pharmacia lettre. 6(6). 380–388. 2 indexed citations
3.
Deepa, K. & Y. Lingappa. (2014). Spectrophotometric determination of selenium in industrial and environmental samples using vanillin-2-aminonicotinic acid (VANA). Der pharma chemica. 6(1). 52–60. 3 indexed citations
4.
Deepa, K., et al.. (2014). Spectrophotometric determination of Mercury in environmental samples using 5-methylthiophene-2-carboxaldehyde ethylenediamine (MTCED). Der pharma chemica. 6(3). 48–55. 3 indexed citations
6.
Deepa, K. & Y. Lingappa. (2014). A simple spectrophotometric method for the determination of arsenic in industrial and environmental samples using 2,4-Dihydroxy benzophenone-2-amino thiophenol. Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy. 124. 102–107. 11 indexed citations
7.
Reddy, G. Rajeshwar, Chandana Lakshmi T. Meda, Kishore V. L. Parsa, et al.. (2013). Montmorillonite K-10 catalyzed green synthesis of 2,6-unsubstituted dihydropyridines as potential inhibitors of PDE4. European Journal of Medicinal Chemistry. 62. 395–404. 19 indexed citations
9.
Reddy, G. Rajeshwar, Y. Lingappa, D. Rambabu, et al.. (2012). Construction of a quinoline ring via a 3-component reaction in water: crystal structure analysis and H-bonding patterns of a 2-aryl quinoline. Green Chemistry. 14(7). 1870–1870. 34 indexed citations
11.
Reddy, G. Rajeshwar, Y. Lingappa, Ravikumar Kapavarapu, et al.. (2011). Montmorillonite K-10 mediated green synthesis of cyano pyridines: Their evaluation as potential inhibitors of PDE4. European Journal of Medicinal Chemistry. 48. 265–274. 23 indexed citations
12.
Reddy, G. Rajeshwar, et al.. (2011). A Pd-mediated new strategy to functionalized 2-aminochromenes: Their in vitro evaluation as potential anti tuberculosis agents. Bioorganic & Medicinal Chemistry Letters. 21(21). 6433–6439. 27 indexed citations
14.
Reddy, N. C. Gangi, et al.. (2011). Chemoselective Synthesis of 2-Aryl-1-arylmethyl-1H-benzo[d]imidazoles Using Indion 190 Resin as a Heterogeneous Recyclable Catalyst. Journal of the Korean Chemical Society. 55(2). 304–307. 8 indexed citations
15.
Reddy, N. C. Gangi, et al.. (2010). A Simple and Convenient Synthesis of (±)-Methylcyclopentanone-3-carboxylate; an Important Precursor of Antitumor Drug Sarkomycin. Bulletin of the Korean Chemical Society. 31(6). 1732–1734.
16.
Rao, K. Srinivasa, T. Balaji, Y. Lingappa, et al.. (2010). Synthesis and characterization of chemically ordered FePt magnetic nano-particles. Physica B Condensed Matter. 405(16). 3205–3207. 6 indexed citations
17.
Subrahmanyam, P., Suvardhan Kanchi, P. Murali Krishna, et al.. (2006). Spectrophotometric Determination of Se (IV) in Environmental Samples Using a Novel Oxidative Coupling Reagent. Environmental Monitoring and Assessment. 123(1-3). 431–437. 1 indexed citations
18.
Lingappa, Y., et al.. (2006). Synthesis, characterization and biological activity of phthalimide derivatives of Cu(II) complex. Radiation effects and defects in solids. 162(1). 11–16. 5 indexed citations
19.
Reddy, K. Hussain & Y. Lingappa. (1993). Spectral and thermal studies on mixed lignad complexes of zinc(II) and cadmium (II) with diethyldithiocarbamate and 2,2′-bipyridyl/1,10-phenanthroline. Journal of Chemical Sciences. 105(2). 87–94. 9 indexed citations
20.
Lingappa, Y.. (1987). Analytical properties of 2-nitro-5,6-dimethyl-1,3-indanedione dithiosemicarbazone. Talanta. 34(9). 789–792. 3 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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