M. Muthukrishnan

824 total citations
45 papers, 652 citations indexed

About

M. Muthukrishnan is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, M. Muthukrishnan has authored 45 papers receiving a total of 652 indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Organic Chemistry, 13 papers in Molecular Biology and 6 papers in Pharmacology. Recurrent topics in M. Muthukrishnan's work include Asymmetric Synthesis and Catalysis (11 papers), Synthesis and biological activity (9 papers) and Synthesis of Indole Derivatives (7 papers). M. Muthukrishnan is often cited by papers focused on Asymmetric Synthesis and Catalysis (11 papers), Synthesis and biological activity (9 papers) and Synthesis of Indole Derivatives (7 papers). M. Muthukrishnan collaborates with scholars based in India, Australia and United States. M. Muthukrishnan's co-authors include Sachin R. Shirsath, Aslam C. Shaikh, Mohammad Mujahid, Perumal Yogeeswari, Ramesh A. Joshi, Om V. Singh, Dharmarajan Sriram, Rajesh G. Gonnade, Milind D. Nikalje and B.E. Stine and has published in prestigious journals such as SHILAP Revista de lepidopterología, Chemical Communications and The Journal of Organic Chemistry.

In The Last Decade

M. Muthukrishnan

45 papers receiving 628 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Muthukrishnan India 15 468 115 107 83 48 45 652
Yanwei Hu China 12 260 0.6× 101 0.9× 55 0.5× 19 0.2× 36 0.8× 25 445
H. A. Ioannidou Cyprus 14 421 0.9× 169 1.5× 63 0.6× 81 1.0× 20 0.4× 24 601
Rahul Singh India 12 204 0.4× 84 0.7× 205 1.9× 27 0.3× 62 1.3× 40 530
Mardia T. El Sayed Egypt 13 332 0.7× 107 0.9× 63 0.6× 47 0.6× 14 0.3× 37 516
Raghunath B. Toche India 14 511 1.1× 98 0.9× 29 0.3× 58 0.7× 24 0.5× 59 614
Samet Mert Türkiye 13 304 0.6× 156 1.4× 43 0.4× 62 0.7× 22 0.5× 23 422
Clinton D. Snyder United States 11 210 0.4× 92 0.8× 161 1.5× 39 0.5× 77 1.6× 20 531
Nagy M. Khalifa Egypt 15 583 1.2× 139 1.2× 60 0.6× 67 0.8× 16 0.3× 77 727
А. В. Богданов Russia 15 495 1.1× 192 1.7× 33 0.3× 39 0.5× 13 0.3× 84 603
Zhixu Zhou China 11 284 0.6× 134 1.2× 42 0.4× 17 0.2× 23 0.5× 66 475

Countries citing papers authored by M. Muthukrishnan

Since Specialization
Citations

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

Fields of papers citing papers by M. Muthukrishnan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Muthukrishnan

This figure shows the co-authorship network connecting the top 25 collaborators of M. Muthukrishnan. A scholar is included among the top collaborators of M. Muthukrishnan 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 M. Muthukrishnan. M. Muthukrishnan 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.
Gayathri, Parthasarathy, et al.. (2024). Visible‐Light Mediated C‐3 Amination of Quinoxalin‐ 2(1H)‐ones via Electron Donor‐Acceptor Complexation. Asian Journal of Organic Chemistry. 13(8). 3 indexed citations
2.
Sasi, Philip, et al.. (2024). Design, Synthesis, and In-vitro anti-tuberculosis activity of 2-substituted-1,5-diphenyl-1,2-dihydro-3H-1,2,4-triazole-3-thione Derivatives. Journal of Physics Conference Series. 2801(1). 12016–12016. 1 indexed citations
3.
Muthukrishnan, M., et al.. (2023). BF3⋅Et2O‐Catalyzed Selective C‐4 Alkylation of Isoquinolin‐1(2H)‐ones Employing p‐Quinone Methides. Chemistry - An Asian Journal. 18(17). e202300546–e202300546. 2 indexed citations
4.
Shirsath, Sachin R., et al.. (2023). Metal- and Photocatalyst-Free, Visible-Light-Initiated C3 α-Aminomethylation of Quinoxalin-2(1H)-ones via Electron Donor–Acceptor Complexes. The Journal of Organic Chemistry. 88(18). 13339–13350. 15 indexed citations
5.
6.
Muthukrishnan, M., et al.. (2019). Efficient Synthesis of Optically Active Neolignans Ligraminol D and E. Synthesis. 51(22). 4291–4295. 1 indexed citations
7.
Shirsath, Sachin R., et al.. (2018). Accessing α-Arylated Nitriles via BF3·OEt2 Catalyzed Cyanation of para-Quinone Methides Using tert-Butyl Isocyanide as a Cyanide Source. The Journal of Organic Chemistry. 83(19). 12305–12314. 45 indexed citations
8.
Mujahid, Mohammad, et al.. (2016). A new and efficient enantioselective synthesis of both enantiomers of the calcium channel blocker bepridil. New Journal of Chemistry. 41(2). 824–829. 5 indexed citations
9.
Vyas, Renu, et al.. (2015). Pharmacophore and Docking Based Virtual Screening of Validated Mycobacterium tuberculosis Targets. Combinatorial Chemistry & High Throughput Screening. 18(7). 624–637. 1 indexed citations
10.
Mujahid, Mohammad, Perumal Yogeeswari, Dharmarajan Sriram, et al.. (2015). Spirochromone-chalcone conjugates as antitubercular agents: synthesis, bio evaluation and molecular modeling studies. RSC Advances. 5(129). 106448–106460. 35 indexed citations
11.
12.
Gonnade, Rajesh G., et al.. (2013). Synthesis and antitubercular activity of amino alcohol fused spirochromone conjugates. Bioorganic & Medicinal Chemistry Letters. 23(5). 1416–1419. 29 indexed citations
13.
Muthukrishnan, M., et al.. (2010). Simple and Efficient Synthesis of 2-Aryl-2,3-Dihydroquinolin-4(1 H )-ones Using Silica Chloride as a New Catalyst Under Solvent-Free Conditions. Synthetic Communications. 40(9). 1391–1398. 10 indexed citations
14.
Nikalje, Milind D., et al.. (2009). A convenient synthesis of enantiomerically pure (R)-mexiletine using hydrolytic kinetic resolution method. Tetrahedron Asymmetry. 20(24). 2814–2817. 20 indexed citations
15.
Muthukrishnan, M., et al.. (2007). Concise synthesis of β-blockers (S)-metoprolol and (S)-betaxolol using hydrolytic kinetic resolution. Tetrahedron. 63(8). 1872–1876. 32 indexed citations
16.
Singh, Om V., et al.. (2005). Synthesis of isoflavones containing naturally occurring substitution pattern by oxidative rearrangement of respective flavanones using thallium(III) p-tosylate §. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 44(12). 2575–2581. 6 indexed citations
17.
Joshi, Ramesh A., et al.. (2005). A convenient synthesis of the enantiomerically pure β-blocker (S)-betaxolol using hydrolytic kinetic resolution. Tetrahedron Asymmetry. 16(23). 3802–3806. 20 indexed citations
18.
Muthukrishnan, M., et al.. (2005). Facile oxidation of flavanones to flavones using [hydroxy(tosyloxy)iodo]benzene in an ionic liquid. Mendeleev Communications. 15(3). 100–101. 11 indexed citations
19.
Joshi, Ramesh A., et al.. (2003). Copper-mediated coupling of aminopurines and aminopyrimidines with arylboronic acids. Tetrahedron Letters. 45(1). 195–197. 12 indexed citations
20.
Stine, B.E., Duane S. Boning, J.E. Chung, et al.. (1998). The physical and electrical effects of metal-fill patterning practices for oxide chemical-mechanical polishing processes. IEEE Transactions on Electron Devices. 45(3). 665–679. 112 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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