Srihari Pabbaraja

3.3k total citations
157 papers, 2.7k citations indexed

About

Srihari Pabbaraja is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Srihari Pabbaraja has authored 157 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 131 papers in Organic Chemistry, 41 papers in Molecular Biology and 29 papers in Pharmacology. Recurrent topics in Srihari Pabbaraja's work include Synthetic Organic Chemistry Methods (64 papers), Chemical synthesis and alkaloids (25 papers) and Microbial Natural Products and Biosynthesis (24 papers). Srihari Pabbaraja is often cited by papers focused on Synthetic Organic Chemistry Methods (64 papers), Chemical synthesis and alkaloids (25 papers) and Microbial Natural Products and Biosynthesis (24 papers). Srihari Pabbaraja collaborates with scholars based in India, United States and France. Srihari Pabbaraja's co-authors include J. S. Yadav, Goverdhan Mehta, Ramesh Samineni, Dinesh C. Bhunia, Shweta Singh, S. Chandrasekhar, Vinay Kumar Singh, Bogonda Ganganna, P. Sreedhar and Subhrangsu S. Mandal and has published in prestigious journals such as Angewandte Chemie International Edition, SHILAP Revista de lepidopterología and Chemical Communications.

In The Last Decade

Srihari Pabbaraja

150 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Srihari Pabbaraja India 31 2.3k 637 381 299 191 157 2.7k
Pallab Pahari India 24 1.3k 0.6× 664 1.0× 609 1.6× 241 0.8× 146 0.8× 57 2.0k
J. S. Yadav India 29 2.6k 1.1× 639 1.0× 319 0.8× 221 0.7× 194 1.0× 144 2.8k
Mukund K. Gurjar India 26 2.1k 0.9× 908 1.4× 339 0.9× 371 1.2× 130 0.7× 164 2.4k
Mathias Christmann Germany 34 3.0k 1.3× 1.1k 1.7× 529 1.4× 331 1.1× 570 3.0× 122 3.9k
Dipakranjan Mal India 23 1.9k 0.8× 320 0.5× 259 0.7× 164 0.5× 160 0.8× 105 2.2k
Mingji Dai United States 33 2.4k 1.1× 712 1.1× 287 0.8× 197 0.7× 287 1.5× 99 3.3k
Willi M. Amberg Switzerland 16 1.6k 0.7× 658 1.0× 196 0.5× 180 0.6× 304 1.6× 27 2.2k
Marco Santagostino Italy 15 1.5k 0.7× 449 0.7× 177 0.5× 212 0.7× 175 0.9× 32 1.8k
Xinfu Pan China 24 1.3k 0.6× 536 0.8× 257 0.7× 173 0.6× 164 0.9× 129 1.8k
Jiahua Chen China 31 2.6k 1.2× 704 1.1× 281 0.7× 217 0.7× 262 1.4× 98 3.0k

Countries citing papers authored by Srihari Pabbaraja

Since Specialization
Citations

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

Fields of papers citing papers by Srihari Pabbaraja

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Srihari Pabbaraja

This figure shows the co-authorship network connecting the top 25 collaborators of Srihari Pabbaraja. A scholar is included among the top collaborators of Srihari Pabbaraja 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 Srihari Pabbaraja. Srihari Pabbaraja 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
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Andugulapati, Sai Balaji, et al.. (2024). Glucosyltriazole amphiphile treatment attenuates breast cancer by modulating the AMPK signaling. Drug Development Research. 85(4). e22215–e22215. 3 indexed citations
3.
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Chakravarty, Sumana, et al.. (2024). One flask cascade approach to a complex pyrano[2,3-c]pyrazole-pyrazolone hybrid heterocyclic system and its initiatory neurobiological profiling. Chemical Communications. 60(64). 8443–8446. 1 indexed citations
5.
Sengupta, Saumitra, Srihari Pabbaraja, & Goverdhan Mehta. (2024). Natural products from the human microbiome: an emergent frontier in organic synthesis and drug discovery. Organic & Biomolecular Chemistry. 22(20). 4006–4030. 4 indexed citations
6.
Pabbaraja, Srihari, et al.. (2024). Visible-light-mediated flow protocol for Achmatowicz rearrangement. Beilstein Journal of Organic Chemistry. 20. 2493–2499.
7.
Nayak, Veena, et al.. (2023). Design, synthesis and biological evaluation of novel cationic liposomes loaded with melphalan for the treatment of cancer. Bioorganic & Medicinal Chemistry Letters. 97. 129549–129549. 3 indexed citations
8.
Roch, Myriam Le, et al.. (2023). Accessing spiropiperidines from dihydropyridones through tandem triflation–allylation and ring-closing metathesis (RCM). Organic & Biomolecular Chemistry. 21(25). 5245–5253. 2 indexed citations
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Sengupta, Saumitra, Srihari Pabbaraja, & Goverdhan Mehta. (2023). C–H modification of natural products: a minimalist enabling tactic for drug discovery, API processing and bioconjugation. Chemical Communications. 59(62). 9445–9456. 2 indexed citations
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Ramprasad, Jurupula, et al.. (2019). Synthesis and evaluation of a novel quinoline-triazole analogs for antitubercular properties via molecular hybridization approach. Bioorganic & Medicinal Chemistry Letters. 29(20). 126671–126671. 50 indexed citations
13.
Singh, Shweta, Ramesh Samineni, Srihari Pabbaraja, & Goverdhan Mehta. (2018). Nitromethane as a Carbanion Source for Domino Benzoannulation with Ynones: One‐Pot Synthesis of Polyfunctional Naphthalenes and a Total Synthesis of Macarpine. Angewandte Chemie. 130(51). 17089–17093. 6 indexed citations
14.
Reddy, Velma Ganga, Srinivasa Reddy Bonam, T. Srinivasa Reddy, et al.. (2017). 4 β -amidotriazole linked podophyllotoxin congeners: DNA topoisomerase-IIα inhibition and potential anticancer agents for prostate cancer. European Journal of Medicinal Chemistry. 144. 595–611. 57 indexed citations
15.
Yadav, J. S., et al.. (2016). Expedient Synthesis of Large‐Ring trans‐Enamide Macrolides by CuI‐Mediated Intramolecular Coupling of Vinyl Iodide with Amide: Total Synthesis of Palmyrolide A. European Journal of Organic Chemistry. 2016(14). 2509–2513. 12 indexed citations
16.
Pabbaraja, Srihari, et al.. (2014). An expedient total synthesis of mupirocin H. RSC Advances. 4(71). 37629–37629. 8 indexed citations
17.
Yadav, J. S., et al.. (2008). The Concise Synthesis of a Key Intermediate for the Total Synthesis of Fumagillin, TNP-470, and Ovalicin. Synthesis. 2008(9). 1460–1466. 5 indexed citations
18.
Chandrasekhar, S., Bathini Nagendra Babu, M. Venkat Ram Reddy, et al.. (2004). Safe and Convenient Reduction of Δ2-Isoxazolines with PMHS-Pd(OH)2/C. Synlett. 1303–1305. 10 indexed citations
19.
Chandrasekhar, S., et al.. (2001). New and practical synthesis of 1,4-dihydrobenzopyrano-pyrazoles. Tetrahedron Letters. 42(37). 6599–6601. 10 indexed citations
20.
Yadav, J. S., Basi V. Subba Reddy, & Srihari Pabbaraja. (2001). ChemInform Abstract: Scandium Triflate Catalyzed Allylation of Acetals and gem‐Diacetates: A Facile Synthesis of Homoallyl Ethers and Acetates.. ChemInform. 32(33). 1 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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