H. M. Meshram

902 total citations
40 papers, 768 citations indexed

About

H. M. Meshram is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, H. M. Meshram has authored 40 papers receiving a total of 768 indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Organic Chemistry, 4 papers in Molecular Biology and 2 papers in Pharmacology. Recurrent topics in H. M. Meshram's work include Chemical Synthesis and Reactions (18 papers), Multicomponent Synthesis of Heterocycles (14 papers) and Synthesis of Indole Derivatives (10 papers). H. M. Meshram is often cited by papers focused on Chemical Synthesis and Reactions (18 papers), Multicomponent Synthesis of Heterocycles (14 papers) and Synthesis of Indole Derivatives (10 papers). H. M. Meshram collaborates with scholars based in India, United States and United Kingdom. H. M. Meshram's co-authors include Rajender S. Varma, B. Chennakesava Reddy, G. Santosh Kumar, J. S. Yadav, Pedavenkatagari Narayana Reddy, N. Nageswara Rao, K. Sadashiv, P. Ramesh, Rajender Dahiya and Ähmed Kamal and has published in prestigious journals such as Tetrahedron, Tetrahedron Letters and Synthesis.

In The Last Decade

H. M. Meshram

39 papers receiving 745 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H. M. Meshram India 16 729 106 99 44 44 40 768
Zhenjun Mao China 12 654 0.9× 75 0.7× 71 0.7× 29 0.7× 40 0.9× 15 687
Nandkishor N. Karade India 16 695 1.0× 74 0.7× 82 0.8× 45 1.0× 52 1.2× 50 737
Najmeh Nowrouzi Iran 13 558 0.8× 109 1.0× 81 0.8× 24 0.5× 48 1.1× 54 606
Sabrina Di Giuseppe Italy 9 962 1.3× 114 1.1× 157 1.6× 25 0.6× 59 1.3× 13 992
N. Suryakiran India 15 589 0.8× 138 1.3× 80 0.8× 18 0.4× 62 1.4× 42 662
Mingji Dai China 8 775 1.1× 103 1.0× 81 0.8× 31 0.7× 63 1.4× 10 823
Vinod T. Kamble India 16 704 1.0× 118 1.1× 36 0.4× 38 0.9× 58 1.3× 63 738
H. M. Meshram India 15 590 0.8× 138 1.3× 121 1.2× 12 0.3× 36 0.8× 30 628
Luis Botella Spain 8 995 1.4× 107 1.0× 95 1.0× 21 0.5× 88 2.0× 13 1.0k
Manas K. Basu United States 13 440 0.6× 94 0.9× 85 0.9× 15 0.3× 42 1.0× 22 486

Countries citing papers authored by H. M. Meshram

Since Specialization
Citations

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

Fields of papers citing papers by H. M. Meshram

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. M. Meshram

This figure shows the co-authorship network connecting the top 25 collaborators of H. M. Meshram. A scholar is included among the top collaborators of H. M. Meshram 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 H. M. Meshram. H. M. Meshram 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.
Meshram, H. M., et al.. (2018). Formal Synthesis of Angiopterlactone B via Enantioselective Reduction of Ketone with Daucus Carota Root. ChemistrySelect. 3(5). 1517–1520. 5 indexed citations
2.
Kumar, Santosh, et al.. (2017). N‐Bromosuccinimide Promoted Direct Thiolation of Imidazoheteroaryl C‐H bonds with Disulfides. ChemistrySelect. 2(4). 1544–1547. 14 indexed citations
3.
Meshram, H. M., et al.. (2017). A rapid and highly efficient Michael addition of methoxybenzenes and indoles to α,β-unsaturated ketones using BF 3 ·OEt 2 as a catalyst. Tetrahedron Letters. 58(47). 4427–4431. 6 indexed citations
4.
Sridevi, B., Yellaiah Tangella, Korrapati Suresh Babu, et al.. (2017). Sulfamic acid catalyzed one-pot, three-component green approach: synthesis and cytotoxic evaluation of pyrazolyl-thiazole congeners. New Journal of Chemistry. 41(10). 3745–3749. 19 indexed citations
5.
Meshram, H. M., et al.. (2017). Toward the Stereoselective Synthesis of Arthrobotrisin A: Fragment Synthesis and Coupling Studies. Synlett. 28(9). 1046–1050. 9 indexed citations
6.
Meshram, H. M., et al.. (2017). Formal synthesis of 14-membered unsymmetrical bis-macrolactone, (−)-colletodiol. Tetrahedron Letters. 58(50). 4687–4690. 5 indexed citations
7.
8.
9.
Meshram, H. M., et al.. (2013). Note Boric acid promoted convenient synthesis of bis (indolyl) methane in aqueous medium. 1 indexed citations
10.
Meshram, H. M., et al.. (2013). l-Proline catalyzed efficient and convenient synthesis of substituted 2H-chromenes by three-component reaction. Tetrahedron Letters. 55(6). 1127–1131. 32 indexed citations
11.
Meshram, H. M., et al.. (2012). Boric acid promoted an efficient and practical synthesis of fused pyrimidines in aqueous media. Der pharma chemica. 4(3). 956–960. 10 indexed citations
12.
Meshram, H. M., et al.. (2012). An efficient synthesis of hemiaminal of indoles by using tetrabutylammonium fluoride (TBAF) in water as a reusable reaction media. Green Chemistry Letters and Reviews. 6(1). 95–100. 8 indexed citations
13.
Meshram, H. M., et al.. (2012). First total synthesis of salinipyrone A using highly stereoselective vinylogous Mukaiyama aldol reaction. Tetrahedron. 68(45). 9289–9292. 15 indexed citations
14.
Meshram, H. M., G. Santosh Kumar, P. Ramesh, & B. Chennakesava Reddy. (2010). A mild and convenient synthesis of quinoxalines via cyclization–oxidation process using DABCO as catalyst. Tetrahedron Letters. 51(19). 2580–2585. 67 indexed citations
15.
Meshram, H. M., et al.. (2010). A green approach for efficient synthesis of N-substituted pyrroles in ionic liquid under microwave irradiation. Tetrahedron Letters. 51(27). 3477–3480. 59 indexed citations
16.
Meshram, H. M., N. Nageswara Rao, & G. Santosh Kumar. (2010). Boric Acid–Mediated Mild and Efficient Friedel–Crafts Alkylation of Indoles with Nitro Styrenes. Synthetic Communications. 40(23). 3496–3500. 13 indexed citations
17.
Meshram, H. M., et al.. (2007). Perchloric Acid Supported on Silica Catalyzed Efficient Synthesis of 1,5‐Benzodiazepines. Synthetic Communications. 37(23). 4117–4122. 9 indexed citations
18.
Meshram, H. M., et al.. (2006). Microwave thermolysis-Part IX: A selective and rapid oxidation of benzylic alcohols using clay supported ammonium nitrate. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 45(2). 500–502. 1 indexed citations
19.
Varma, Rajender S. & H. M. Meshram. (1997). Solid State Cleavage of Semicarbazones and Phenylhydrazones with Ammonium Persulfate-Clay using Microwave or Ultrasonic Irradiation. Tetrahedron Letters. 38(46). 7973–7976. 78 indexed citations
20.
Kamal, Ähmed, M. V. Prabhakara Rao, & H. M. Meshram. (1991). Enzymatic deoximation of oximes by ultrasonically stimulated baker's yeast. Journal of the Chemical Society Perkin Transactions 1. 2056–2056. 26 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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