Sanjeev Kanojiya

1.0k total citations
58 papers, 805 citations indexed

About

Sanjeev Kanojiya is a scholar working on Molecular Biology, Organic Chemistry and Plant Science. According to data from OpenAlex, Sanjeev Kanojiya has authored 58 papers receiving a total of 805 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 19 papers in Organic Chemistry and 11 papers in Plant Science. Recurrent topics in Sanjeev Kanojiya's work include Phytochemistry and Bioactive Compounds (8 papers), Synthesis of heterocyclic compounds (8 papers) and Natural product bioactivities and synthesis (6 papers). Sanjeev Kanojiya is often cited by papers focused on Phytochemistry and Bioactive Compounds (8 papers), Synthesis of heterocyclic compounds (8 papers) and Natural product bioactivities and synthesis (6 papers). Sanjeev Kanojiya collaborates with scholars based in India, Nepal and Poland. Sanjeev Kanojiya's co-authors include Prem P. Yadav, Sanjay Batra, Dipak Kumar Mishra, Jayanta Sarkar, Sudhir Sinha, Ranjani Maurya, Ashish Arora, K. P. Madhusudanan, Vineeta Tripathi and Shashikant U. Dighe and has published in prestigious journals such as Angewandte Chemie International Edition, Scientific Reports and The Journal of Organic Chemistry.

In The Last Decade

Sanjeev Kanojiya

53 papers receiving 777 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sanjeev Kanojiya India 17 345 280 188 146 86 58 805
Supreeya Yuenyongsawad Thailand 18 263 0.8× 249 0.9× 202 1.1× 289 2.0× 53 0.6× 38 971
Zhi‐You Hao China 16 456 1.3× 265 0.9× 282 1.5× 91 0.6× 42 0.5× 54 902
Suwanna Deachathai Thailand 14 254 0.7× 190 0.7× 317 1.7× 114 0.8× 37 0.4× 26 663
Márcia Aparecida Antônio Brazil 11 271 0.8× 243 0.9× 225 1.2× 69 0.5× 37 0.4× 26 813
Natthinee Anantachoke Thailand 14 259 0.8× 121 0.4× 271 1.4× 133 0.9× 31 0.4× 32 646
Yasin Genç Türkiye 10 280 0.8× 226 0.8× 246 1.3× 129 0.9× 32 0.4× 19 805
Phu Hoang Dang Vietnam 17 416 1.2× 111 0.4× 173 0.9× 141 1.0× 47 0.5× 78 750
Surya Kant Kalauni Nepal 18 508 1.5× 251 0.9× 252 1.3× 396 2.7× 42 0.5× 54 1.1k
Francisco Rivas Spain 20 689 2.0× 154 0.6× 129 0.7× 112 0.8× 60 0.7× 55 944
Khursheed Ahmad Bhat India 16 345 1.0× 199 0.7× 228 1.2× 113 0.8× 26 0.3× 51 804

Countries citing papers authored by Sanjeev Kanojiya

Since Specialization
Citations

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

Fields of papers citing papers by Sanjeev Kanojiya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sanjeev Kanojiya

This figure shows the co-authorship network connecting the top 25 collaborators of Sanjeev Kanojiya. A scholar is included among the top collaborators of Sanjeev Kanojiya 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 Sanjeev Kanojiya. Sanjeev Kanojiya 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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Rawat, Priyanka, et al.. (2023). Comprehensive characterization of Dactylorhin and loroglossin in Dactylorhiza hatagirea D. DON using ultra-performance liquid chromatography-mass spectrometry. International Journal of Mass Spectrometry. 490. 117069–117069. 1 indexed citations
3.
Bisen, Amol Chhatrapati, Sachin Nashik Sanap, Sristi Agrawal, et al.. (2023). Hesperidin: Enrichment, forced degradation, and structural elucidation of potential degradation products using spectral techniques. Rapid Communications in Mass Spectrometry. 37(20). e9615–e9615. 6 indexed citations
4.
Prakash, Ravi, et al.. (2023). Bone Fracture-healing Properties and UPLC-MS Analysis of an Enriched Flavonoid Fraction from Oxystelma esculentum. Planta Medica. 90(2). 96–110. 1 indexed citations
5.
Kanojiya, Sanjeev, et al.. (2023). Effect of Methyl Jasmonate and Salicylic Acid on the Enrichment of Carbazole Alkaloids in Murraya koenigii (L.) Spreng. Journal of Plant Growth Regulation. 43(9). 3192–3203. 1 indexed citations
6.
Ahmad, Shadab, Suriya P. Singh, Anjali Mishra, et al.. (2022). Furostanol saponins from Asparagus racemosus as potential hypoglycemic agents. Phytochemistry. 201. 113286–113286. 14 indexed citations
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Mishra, Dipak Kumar, et al.. (2019). Standardization of enrichment protocols for some medicinally important cardenolides within in vitro grown Calotropis gigantea plantlets. Pharmacognosy Magazine. 15(61). 264–264. 5 indexed citations
9.
Gupta, Abhishek, Ashok Kumar, Durgesh Kumar, et al.. (2017). Ethyl acetate fraction of Eclipta alba: a potential phytopharmaceutical targeting adipocyte differentiation. Biomedicine & Pharmacotherapy. 96. 572–583. 14 indexed citations
10.
Kanojiya, Sanjeev, et al.. (2016). Identification of an antibacterial Withanolide (Dinoxin B) from leaf of Datura inoxia Mill.. International Journal of Phytomedicine. 8(1). 1–12. 4 indexed citations
11.
Dighe, Shashikant U., et al.. (2015). Synthesis of 3,4,5‐Trisubstituted Isoxazoles from Morita–Baylis–Hillman Acetates by an NaNO2/I2‐Mediated Domino Reaction. Angewandte Chemie International Edition. 54(37). 10926–10930. 45 indexed citations
12.
Dighe, Shashikant U., et al.. (2015). Synthesis of 3,4,5‐Trisubstituted Isoxazoles from Morita–Baylis–Hillman Acetates by an NaNO2/I2‐Mediated Domino Reaction. Angewandte Chemie. 127(37). 11076–11080. 11 indexed citations
13.
Mahar, Rohit, et al.. (2015). Quantitative Analysis of Bioactive Carbazole Alkaloids in Murraya koenigii. Natural Product Communications. 10(2). 293–5. 3 indexed citations
14.
Kanojiya, Sanjeev, et al.. (2014). Callus culture and in vitro biosynthesis of echitamine from Alstonia scholaris (L.) R. Br.. Plant Cell Tissue and Organ Culture (PCTOC). 120(1). 367–372. 6 indexed citations
15.
Adaramoye, Oluwatosin A., Jayanta Sarkar, Neetu Singh, et al.. (2011). Antiproliferative Action of Xylopia aethiopica Fruit Extract on Human Cervical Cancer Cells. Phytotherapy Research. 25(10). 1558–1563. 60 indexed citations
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Yadav, Prem P., Ranjani Maurya, Jayanta Sarkar, et al.. (2009). Cassane Diterpenes from Caesalpinia bonduc. Phytochemistry. 70(2). 256–261. 63 indexed citations
18.
Madhusudanan, K. P., Brijesh Kumar, Sanjeev Kanojiya, Geetanjali Agnihotri, & Anup Kumar Misra. (2006). Tandem mass spectra of divalent metal ion adducts of glycosyl sulfides, sulfoxides and sulfones; distinction among stereoisomers. Journal of Mass Spectrometry. 41(10). 1322–1333. 6 indexed citations
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Madhusudanan, K. P., et al.. (2005). Effect of stereochemistry on the electrospray ionization tandem mass spectra of transition metal chloride complexes of monosaccharides. Journal of Mass Spectrometry. 40(8). 1044–1054. 9 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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