V. P. Vaidya
About
In The Last Decade
V. P. Vaidya
51 papers receiving 706 citations
Peers
Comparison fields: 5 of 75
- Organic Chemistry 569
- Molecular Biology 133
- Plant Science 98
- Pharmacology 69
- Endocrinology, Diabetes and Metabolism 44
Countries citing papers authored by V. P. Vaidya
This map shows the geographic impact of V. P. Vaidya'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 V. P. Vaidya with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites V. P. Vaidya more than expected).
Fields of papers citing papers by V. P. Vaidya
This network shows the impact of papers produced by V. P. Vaidya. 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 V. P. Vaidya. The network helps show where V. P. Vaidya may publish in the future.
Co-authorship network of co-authors of V. P. Vaidya
This figure shows the co-authorship network connecting the top 25 collaborators of V. P. Vaidya. A scholar is included among the top collaborators of V. P. Vaidya 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 V. P. Vaidya. V. P. Vaidya is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | SYNTHESIS AND STRUCTURAL STUDIES OF 1-[(8-NITRONAPHTHO[2,1-B]FURAN-2-YL) CARBONYL] PIPERIDINE | 0 |
| 3 | 2 | |
| 4 | In vitro anthelmintic activity of leaves extract of Wrightia tinctoria. | 2 |
| 5 | Synthesis and Antimicrobial Evaluation of Some New Pyrrolylnaphtho[2,1-b] furan Derivatives | 1 |
| 6 | Synthesis, biological and pharmacological activities of 2-methyl-4H-pyrimido[2,1-b][1,3]benzothiazoles. | 14 |
| 7 | Synthesis, characterization and pharmacological studies on some triazolothiadiazines and triazolothiadiazoles containing naphtho[2,b]furan | 4 |
| 8 | Synthesis of novel naphtho(2,1-b)furo(3,2-b)pyridine derivatives as potential antimicrobial agents | 8 |
| 9 | 40 | |
| 10 | 12 | |
| 11 | Synthesis, antimicrobial and antiinflammatory activities of 1,3,4-oxadiazoles linked to naphtho[2,1- b ]furan | 12 |
| 12 | Screening of Momordica dioica for hepatoprotective, antioxidant, and antiinflammatory activities | 7 |
| 13 | A new flavonoid from Momordica dioica Roxb | 1 |
| 14 | Microwave assisted one pot synthesis of 8-methyl-3,6,9-triphenyl-5,6-dihydro-9 H -pyrazolo[3,4- e ][1,2,4]triazolo[3,4- b ][1,3,4]thiadiazepine | 1 |
| 15 | Synthesis of novel naphtho[2,1- b ]furo pyrazolyl, isoxazolyl and pyridyl derivatives as potential antimicrobial agents | 1 |
| 16 | Synthesis of novel angularly fused pentacyclic heterocycles of pharmacological interest | 3 |
| 17 | Synthesis of naphtho[2,1-b]furo[3,2-e]-1,4-diazepin-2-ones and naphtho[2,1- b]furo[3,2-e]-1,3,4-triazepin-2-ones of pharmacological interest | 3 |
| 18 | Evaluation of some novel heterocyclic compounds for antifertility, antiinflammatory and analgesic activities | 1 |
| 19 | Synthesis And Pharmacological Evaluation Of Some Potent Naphtho (2,1-b) Furo-Pyrazolyl, Oxadiazolyl And Coumaryl Derivatives | 9 |
| 20 | Postcoital Antifertility Activity Of The Root Of Momordica Dioica Roxb | 11 |
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.