K. Srinivas

1.6k total citations
79 papers, 1.4k citations indexed

About

K. Srinivas is a scholar working on Organic Chemistry, Molecular Biology and Materials Chemistry. According to data from OpenAlex, K. Srinivas has authored 79 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Organic Chemistry, 30 papers in Molecular Biology and 10 papers in Materials Chemistry. Recurrent topics in K. Srinivas's work include Synthesis and Characterization of Heterocyclic Compounds (15 papers), Chemical Synthesis and Analysis (10 papers) and Multicomponent Synthesis of Heterocycles (8 papers). K. Srinivas is often cited by papers focused on Synthesis and Characterization of Heterocyclic Compounds (15 papers), Chemical Synthesis and Analysis (10 papers) and Multicomponent Synthesis of Heterocycles (8 papers). K. Srinivas collaborates with scholars based in India, France and United States. K. Srinivas's co-authors include V. Jayathirtha Rao, Biswanath Das, K. Bhanuprakash, U. Srinivas, Biswanath Das, U. S. N. Murty, K. Hara Kishore, Ivan Huc, Sanyasi Sitha and Biswanath Das and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Journal of Materials Chemistry.

In The Last Decade

K. Srinivas

78 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
K. Srinivas India 20 856 511 151 121 104 79 1.4k
Hassan M. Faidallah Saudi Arabia 22 1.3k 1.6× 463 0.9× 142 0.9× 95 0.8× 73 0.7× 119 1.6k
Dieter Ströhl Germany 21 547 0.6× 488 1.0× 112 0.7× 71 0.6× 49 0.5× 70 1.1k
M.L. Rodríguez Spain 19 636 0.7× 317 0.6× 77 0.5× 130 1.1× 69 0.7× 66 1.2k
Andreas Speicher Germany 17 1.8k 2.1× 394 0.8× 155 1.0× 96 0.8× 54 0.5× 46 2.3k
Denitsa Yancheva Bulgaria 21 545 0.6× 339 0.7× 93 0.6× 146 1.2× 135 1.3× 106 1.2k
Jacek W. Morzycki Poland 23 701 0.8× 964 1.9× 156 1.0× 128 1.1× 33 0.3× 154 1.8k
Manohar V. Kulkarni India 20 1.4k 1.6× 352 0.7× 312 2.1× 112 0.9× 45 0.4× 100 1.6k
Anne Jäger Germany 24 1.3k 1.5× 321 0.6× 201 1.3× 83 0.7× 51 0.5× 54 1.7k
Florent Di Meo France 22 609 0.7× 405 0.8× 79 0.5× 238 2.0× 52 0.5× 57 1.5k
Rogério Corrêa Brazil 22 578 0.7× 312 0.6× 107 0.7× 112 0.9× 36 0.3× 67 1.1k

Countries citing papers authored by K. Srinivas

Since Specialization
Citations

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

Fields of papers citing papers by K. Srinivas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K. Srinivas

This figure shows the co-authorship network connecting the top 25 collaborators of K. Srinivas. A scholar is included among the top collaborators of K. Srinivas 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 K. Srinivas. K. Srinivas 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.
Ghosh, Kaushik, et al.. (2015). A novel UV degradation product of Ebastine: Isolation and characterization using Q-TOF, NMR, IR and computational chemistry. Journal of Pharmaceutical and Biomedical Analysis. 107. 488–494. 10 indexed citations
2.
Srinivas, K., et al.. (2014). Isolation and characterization of a novel acid degradation impurity of Amlodipine Besylate using Q-TOF, NMR, IR and single crystal X-ray. Journal of Pharmaceutical and Biomedical Analysis. 99. 59–66. 12 indexed citations
3.
Rao, Boddu Ananda, Pankaj Sharma, Dinesh Thummuri, et al.. (2014). Synthesis and biological evaluation of new rhodanine analogues bearing 2-chloroquinoline and benzo[h]quinoline scaffolds as anticancer agents. European Journal of Medicinal Chemistry. 83. 569–580. 51 indexed citations
4.
Ravinder, M., Pankaj K. Bagul, Chandrakant Bagul, et al.. (2013). Synthesis and biological evaluation of new epalrestat analogues as aldose reductase inhibitors (ARIs). European Journal of Medicinal Chemistry. 71. 53–66. 60 indexed citations
5.
Ravinder, M., et al.. (2012). Synthesis and evaluation of novel 2-pyridone derivatives as inhibitors of phosphodiesterase3 (PDE3): A target for heart failure and platelet aggregation. Bioorganic & Medicinal Chemistry Letters. 22(18). 6010–6015. 50 indexed citations
6.
Gara, Rishi K., et al.. (2012). Anticancer siRNA delivery by new anticancer molecule: A novel combination strategy for cancer cell killing. European Journal of Medicinal Chemistry. 56. 400–408. 16 indexed citations
7.
8.
Rao, Boddu Ananda, et al.. (2011). Synthesis And In Vitro Antitumor Activity Of New Nicotinyl-Rhodanine Derivatives. International Journal of Pharma and Bio Sciences. 3 indexed citations
9.
Bao, Chunyan, Brice Kauffmann, Quan Gan, et al.. (2008). Converting Sequences of Aromatic Amino Acid Monomers into Functional Three‐Dimensional Structures: Second‐Generation Helical Capsules. Angewandte Chemie International Edition. 47(22). 4153–4156. 73 indexed citations
10.
Prabhakar, S., et al.. (2007). Mass spectral studies of meso‐dialkyl, alkyl aryl and cycloalkyl calix(4)pyrroles under positive and negative ion electrospray ionization conditions. Journal of Mass Spectrometry. 42(9). 1194–1206. 5 indexed citations
11.
12.
Ravikumar, Κ., et al.. (2006). Chains of edge-fused hydrogen-bondedR33(22) rings in 5,3′-dihydroxy-3,6,7,4′,5′-pentamethoxyflavone. Acta Crystallographica Section C Crystal Structure Communications. 62(8). o495–o497. 1 indexed citations
13.
Srinivas, K., Sanyasi Sitha, V. Jayathirtha Rao, et al.. (2005). First hyperpolarizability of some nonconjugated donor–acceptor 3D molecules: noncentrosymmetric crystal through conformational flexibility. Journal of Materials Chemistry. 15(9). 965–973. 32 indexed citations
14.
Srinivas, K., U. Srinivas, V. Jayathirtha Rao, et al.. (2004). Synthesis and antibacterial activity of 2,4,6-tri substituted s-triazines. Bioorganic & Medicinal Chemistry Letters. 15(4). 1121–1123. 78 indexed citations
15.
Srinivas, K., et al.. (2004). AN IMPROVED SYNTHESIS OF 5-(2-FLUOROPHENYL)-1H-TETRAZOLE. Organic Preparations and Procedures International. 36(1). 69–71. 3 indexed citations
16.
17.
Srinivas, K., et al.. (2003). A facile synthesis of 4-oxo-1,2,3,4-tetrahydropyrido[3¢,2¢:4,5]furo[3,2-d]pyridines: A new tricyclic heterocyclic ring system. (Abstract Only). Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 42(3). 605–610. 3 indexed citations
18.
19.
Das, Biswanath, et al.. (1995). A taxoid from needles of himalayan Taxus baccata. Phytochemistry. 38(3). 671–674. 14 indexed citations
20.
Takhi, Mohamed, et al.. (1994). A lignan from needles of himalayan taxus baccata. Phytochemistry. 36(4). 1031–1033. 14 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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