Padmanava Pradhan

1.3k total citations
49 papers, 1.0k citations indexed

About

Padmanava Pradhan is a scholar working on Organic Chemistry, Molecular Biology and Toxicology. According to data from OpenAlex, Padmanava Pradhan has authored 49 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Organic Chemistry, 19 papers in Molecular Biology and 7 papers in Toxicology. Recurrent topics in Padmanava Pradhan's work include DNA and Nucleic Acid Chemistry (8 papers), Bioactive Compounds and Antitumor Agents (7 papers) and Catalytic C–H Functionalization Methods (7 papers). Padmanava Pradhan is often cited by papers focused on DNA and Nucleic Acid Chemistry (8 papers), Bioactive Compounds and Antitumor Agents (7 papers) and Catalytic C–H Functionalization Methods (7 papers). Padmanava Pradhan collaborates with scholars based in United States, India and Sweden. Padmanava Pradhan's co-authors include Mahesh K. Lakshman, Asoke Banerji, Ramendra Pratap, Ashoke Deb, Swapnil R. Jadhav, George John, Damon A. Parrish, Ajit K. Parhi, Kurt W. Saionz and Malvika Kaul and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and Angewandte Chemie International Edition.

In The Last Decade

Padmanava Pradhan

49 papers receiving 983 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Padmanava Pradhan United States 18 591 308 100 96 80 49 1.0k
José I. Miranda Spain 20 665 1.1× 286 0.9× 147 1.5× 47 0.5× 47 0.6× 54 1.1k
Deepak K. Sharma India 20 510 0.9× 345 1.1× 164 1.6× 56 0.6× 170 2.1× 96 1.1k
Chun Li United States 14 328 0.6× 323 1.0× 104 1.0× 36 0.4× 63 0.8× 48 761
Fung Fuh Wong Taiwan 20 868 1.5× 225 0.7× 75 0.8× 49 0.5× 50 0.6× 101 1.1k
Tao Deng China 19 323 0.5× 232 0.8× 240 2.4× 78 0.8× 47 0.6× 65 876
Alejandro Bugarin United States 23 901 1.5× 235 0.8× 101 1.0× 37 0.4× 58 0.7× 71 1.3k
Mohammad Rahimizadeh Iran 23 1.3k 2.1× 362 1.2× 194 1.9× 46 0.5× 47 0.6× 124 1.6k
Li Shen China 19 336 0.6× 305 1.0× 433 4.3× 175 1.8× 72 0.9× 67 1.3k
Mihaela Bălan Romania 15 268 0.5× 137 0.4× 123 1.2× 60 0.6× 95 1.2× 58 636
И. В. Заварзин Russia 21 1.2k 2.0× 368 1.2× 276 2.8× 37 0.4× 82 1.0× 214 1.7k

Countries citing papers authored by Padmanava Pradhan

Since Specialization
Citations

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

Fields of papers citing papers by Padmanava Pradhan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Padmanava Pradhan

This figure shows the co-authorship network connecting the top 25 collaborators of Padmanava Pradhan. A scholar is included among the top collaborators of Padmanava Pradhan 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 Padmanava Pradhan. Padmanava Pradhan 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.
Lakshman, Mahesh K., et al.. (2023). Nitrene C−H Bond Insertion Approach to Carbazolones and Indolones, and a Reactivity Departure for 7‐Membered Analogues**. Chemistry - A European Journal. 29(72). e202302995–e202302995. 2 indexed citations
2.
Bae, Suyeal, et al.. (2022). Diversely C8-functionalized adenine nucleosides via their underexplored carboxaldehydes. Chemical Communications. 58(11). 1744–1747. 2 indexed citations
3.
Pradhan, Padmanava, et al.. (2021). General Approach to N6,C5′-Difunctionalization of Adenosine. The Journal of Organic Chemistry. 87(1). 18–39. 5 indexed citations
4.
Petrovic, Ana G., et al.. (2021). Synthesis of Oligonucleotides Containing Trans Mitomycin C DNA Adducts at N6 of Adenine and N2 of Guanine. Chemistry - A European Journal. 27(57). 14263–14272. 4 indexed citations
5.
Aguilera, Renato J., Graciela Andreï, Robert Snoeck, et al.. (2019). Synthesis and Evaluations of “1,4‐Triazolyl Combretacoumarins” and Desmethoxy Analogs. European Journal of Organic Chemistry. 2019(33). 5610–5623. 7 indexed citations
6.
Proni, Gloria, et al.. (2019). Synthesis of Mitomycin C and decarbamoylmitomycin C N6 deoxyadenosine-adducts. Bioorganic Chemistry. 92. 103280–103280. 10 indexed citations
7.
8.
Yang, Lijia, et al.. (2016). A novel bis(pinacolato)diboron-mediated N–O bond deoxygenative route to C6 benzotriazolyl purine nucleoside derivatives. Organic & Biomolecular Chemistry. 14(29). 7069–7083. 8 indexed citations
9.
Pradhan, Padmanava, et al.. (2014). Cycloaddition of Arynes and Cyclic Enol Ethers as a Platform for Access to Stereochemically Defined 1,2‐Disubstituted Benzocyclobutenes. European Journal of Organic Chemistry. 2015(4). 750–764. 14 indexed citations
10.
Parhi, Ajit K., Yong‐Zheng Zhang, Kurt W. Saionz, et al.. (2013). Antibacterial activity of quinoxalines, quinazolines, and 1,5-naphthyridines. Bioorganic & Medicinal Chemistry Letters. 23(17). 4968–4974. 145 indexed citations
11.
Reddy, Arava Leela Mohana, Subbiah Nagarajan, Sanketh R. Gowda, et al.. (2012). Lithium storage mechanisms in purpurin based organic lithium ion battery electrodes. Scientific Reports. 2(1). 960–960. 117 indexed citations
12.
Kumar, Rakesh, Padmanava Pradhan, & Barbara Zajc. (2011). Facile synthesis of 4-vinyl- and 4-fluorovinyl-1,2,3-triazoles via bifunctional “click-olefination” reagents. Chemical Communications. 47(13). 3891–3891. 24 indexed citations
13.
Lakshman, Mahesh K., et al.. (2011). Direct Arylation of 6‐Phenylpurine and 6‐Arylpurine Nucleosides by Ruthenium‐Catalyzed CH Bond Activation. Angewandte Chemie International Edition. 50(48). 11400–11404. 86 indexed citations
14.
Lakshman, Mahesh K., et al.. (2011). Direct Arylation of 6‐Phenylpurine and 6‐Arylpurine Nucleosides by Ruthenium‐Catalyzed CH Bond Activation. Angewandte Chemie. 123(48). 11602–11606. 19 indexed citations
15.
Jadhav, Swapnil R., et al.. (2010). Adhesive Vesicles through Adaptive Response of a Biobased Surfactant. Angewandte Chemie International Edition. 49(49). 9509–9512. 32 indexed citations
16.
Lakshman, Mahesh K., et al.. (2008). Synthesis of N6,N6‐Dialkyladenine Nucleosides Using Hexaalkylphosphorus Triamides Produced in Situ. European Journal of Organic Chemistry. 2009(1). 152–159. 11 indexed citations
17.
Pradhan, Padmanava, Ranajeet Ghose, & Michael E. Green. (2005). Voltage gating and anions, especially phosphate: A model system. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1717(2). 97–103. 8 indexed citations
18.
Bae, Suyeal, et al.. (2005). Synthesis and Reactions of 2-Chloro- and 2-Tosyloxy-2‘-deoxyinosine Derivatives. The Journal of Organic Chemistry. 70(18). 7188–7195. 12 indexed citations
19.
Zhang, Lina, Zhe Li, Jiangli Yan, et al.. (2003). Mutagenesis of the Runt Domain Defines Two Energetic Hot Spots for Heterodimerization with the Core Binding Factor β Subunit. Journal of Biological Chemistry. 278(35). 33097–33104. 24 indexed citations
20.
Pradhan, Padmanava, et al.. (1994). Cordifolisides A, B, C: Norditerpene furan glycosides from Tinospora cordifolia. Phytochemistry. 37(3). 781–786. 35 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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