J. S. Yadav

3.4k total citations
144 papers, 2.8k citations indexed

About

J. S. Yadav is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, J. S. Yadav has authored 144 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 131 papers in Organic Chemistry, 37 papers in Molecular Biology and 23 papers in Pharmacology. Recurrent topics in J. S. Yadav's work include Synthetic Organic Chemistry Methods (54 papers), Chemical Synthesis and Reactions (43 papers) and Asymmetric Synthesis and Catalysis (22 papers). J. S. Yadav is often cited by papers focused on Synthetic Organic Chemistry Methods (54 papers), Chemical Synthesis and Reactions (43 papers) and Asymmetric Synthesis and Catalysis (22 papers). J. S. Yadav collaborates with scholars based in India, France and China. J. S. Yadav's co-authors include B. V. Subba Reddy, B. V. Subba Reddy, Gowravaram Sabitha, Gakul Baishya, K. Nagaiah, A. K. Basak, A. Venkat Narsaiah, Basi V. Subba Reddy, Sunitha Sadula and K. Premalatha and has published in prestigious journals such as Angewandte Chemie International Edition, Green Chemistry and The Journal of Organic Chemistry.

In The Last Decade

J. S. Yadav

139 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. S. Yadav India 29 2.6k 639 319 221 194 144 2.8k
Xuegong She China 35 3.2k 1.2× 596 0.9× 399 1.3× 293 1.3× 287 1.5× 188 3.9k
Rick Danheiser United States 46 4.7k 1.8× 689 1.1× 244 0.8× 168 0.8× 420 2.2× 112 5.3k
José Justicia Spain 28 1.7k 0.7× 390 0.6× 226 0.7× 239 1.1× 364 1.9× 58 2.2k
Giovanni Piancatelli Italy 21 2.3k 0.9× 529 0.8× 183 0.6× 224 1.0× 236 1.2× 94 2.6k
Subhash P. Chavan India 28 2.0k 0.8× 719 1.1× 165 0.5× 106 0.5× 285 1.5× 167 2.6k
Pradeep Kumar India 36 3.2k 1.2× 855 1.3× 358 1.1× 241 1.1× 591 3.0× 171 3.9k
Gowravaram Sabitha India 34 4.0k 1.5× 887 1.4× 606 1.9× 472 2.1× 340 1.8× 233 4.4k
Yoo Tanabe Japan 32 2.5k 1.0× 740 1.2× 140 0.4× 97 0.4× 282 1.5× 140 2.9k
Xinfu Pan China 24 1.3k 0.5× 536 0.8× 257 0.8× 173 0.8× 164 0.8× 129 1.8k
Marco Santagostino Italy 15 1.5k 0.6× 449 0.7× 177 0.6× 212 1.0× 175 0.9× 32 1.8k

Countries citing papers authored by J. S. Yadav

Since Specialization
Citations

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

Fields of papers citing papers by J. S. Yadav

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. S. Yadav. 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 J. S. Yadav. The network helps show where J. S. Yadav may publish in the future.

Co-authorship network of co-authors of J. S. Yadav

This figure shows the co-authorship network connecting the top 25 collaborators of J. S. Yadav. A scholar is included among the top collaborators of J. S. Yadav 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 J. S. Yadav. J. S. Yadav 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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Gohil, Nisarg, Gargi Bhattacharjee, Vijai Singh, et al.. (2024). New Amino Acids Naphthalene Scaffolds as Potent Antimicrobial Agents: In Vitro Assay and In Silico Molecular Docking Study. ChemistrySelect. 9(17). 1 indexed citations
3.
Reddy, B. V. Subba, et al.. (2023). Stereoselective total syntheses of dodoneine and its diastereomer, epidodoneine via Prins cyclisation. Tetrahedron. 132. 133242–133242.
4.
Tadiparthi, Krishnaji, et al.. (2022). Synthetic Applications of Prins Cyclization in Natural Product Syntheses. The Chemical Record. 22(8). e202200044–e202200044. 8 indexed citations
5.
Yadav, J. S., et al.. (2020). Stereoselective Synthesis of the C1–C16 Fragment of the Purported Structure of Formosalide B. ACS Omega. 5(17). 10217–10224. 6 indexed citations
6.
Nagaiah, K., et al.. (2020). Stereoselective Total Synthesis of (‐)‐Ebelactone A. ChemistrySelect. 5(9). 2763–2766.
7.
Yadav, J. S., et al.. (2019). Studies towards the Synthesis of Aldgamycin – M. ChemistrySelect. 4(11). 3002–3005. 8 indexed citations
8.
Das, Saibal, et al.. (2018). Studies towards the Total Synthesis of Aspergillide‐B. ChemistrySelect. 3(12). 3391–3393. 3 indexed citations
9.
Yadav, J. S., Shweta Singh, & Saibal Das. (2018). Stereoselective Total Syntheses of Acutifolone A, Bisacutifolone A and B, Pinguisenol, and Isonaviculol. ACS Omega. 3(1). 636–647. 6 indexed citations
10.
Reddy, B. V. Subba, et al.. (2017). Synthesis and biological evaluation of 1-amino isochromans from 2-bromoethyl benzaldehyde and amines in acid medium. Bioorganic & Medicinal Chemistry Letters. 28(2). 196–201. 5 indexed citations
11.
Sabitha, Gowravaram, et al.. (2010). Enantioselective Synthesis of Herbarumin III by Using a Chelation‐Controlled Reduction. Helvetica Chimica Acta. 93(8). 1634–1640. 5 indexed citations
12.
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Sabitha, Gowravaram, et al.. (2006). VCl3-Catalyzed aza-Diels-Alder reaction: one-pot synthesis of pyrano(3,2-c)quinolines and furo(3,2-c)quinolines. 1 indexed citations
14.
Yadav, J. S., et al.. (2003). Ring expansion approach for the synthesis of the (3S,4S)-hexahydroazepine core of balanol and ophiocordin. Tetrahedron. 59(51). 10325–10329. 29 indexed citations
15.
Yadav, J. S., et al.. (2003). Novel Use of SelectfluorTM for the Synthesis of cis‐Fused Pyrano‐ and Furanotetrahydroquinolines. Advanced Synthesis & Catalysis. 345(11). 1203–1206. 26 indexed citations
16.
Murty, M. S. R., T. Ramalingam, Gowravaram Sabitha, & J. S. Yadav. (2001). Facile Synthesis of 9,10-Dihydro-4H-Benzo [4,5] Cyclohepta [1,2-b] Thiophene-4-One: A Crucial Drug Intermediate-Application of Wittig-Horner Reaction. Heterocyclic Communications. 7(5). 449–454. 2 indexed citations
17.
Yadav, J. S., B. V. Subba Reddy, G. Mahesh Kumar, & Ch. Madan. (2001). InCl3-SiO2 Catalyzed Electrophilic Amination of Arenes: A Facile and Rapid Synthesis of Aryl Hydrazides. Synlett. 2001(11). 1781–1783. 44 indexed citations
18.
Yadav, J. S., et al.. (2000). Synthesis of (3E, 5Z)-3,5-Dodecadienylacetate, the Sex Pheromone ofPhtheochroa cranaodes(Lepidoptera: Tortricidae). Bioscience Biotechnology and Biochemistry. 64(8). 1726–1728. 7 indexed citations
19.
Yadav, J. S., et al.. (1999). A convergent total synthesis of mappicine ketone: A leading antiviral compound. Tetrahedron. 55(17). 5449–5456. 13 indexed citations
20.

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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