Sudhir Nambiar

497 total citations
23 papers, 419 citations indexed

About

Sudhir Nambiar is a scholar working on Organic Chemistry, Molecular Biology and Physical and Theoretical Chemistry. According to data from OpenAlex, Sudhir Nambiar has authored 23 papers receiving a total of 419 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Organic Chemistry, 8 papers in Molecular Biology and 5 papers in Physical and Theoretical Chemistry. Recurrent topics in Sudhir Nambiar's work include Crystallography and molecular interactions (5 papers), Chemical Synthesis and Analysis (4 papers) and Crystallization and Solubility Studies (4 papers). Sudhir Nambiar is often cited by papers focused on Crystallography and molecular interactions (5 papers), Chemical Synthesis and Analysis (4 papers) and Crystallization and Solubility Studies (4 papers). Sudhir Nambiar collaborates with scholars based in India, United States and United Kingdom. Sudhir Nambiar's co-authors include Sulur G. Manjunatha, Ashwini Nangia, N. Rajesh Goud, Kuthuru Suresh, K. Grant Taylor, Ronald J. Doyle, John F. Daeuble, Dongxu Qiu, Stephen Hanessian and Seth Ribe and has published in prestigious journals such as The Journal of Organic Chemistry, Journal of Pharmaceutical Sciences and Tetrahedron Letters.

In The Last Decade

Sudhir Nambiar

23 papers receiving 406 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sudhir Nambiar India 11 189 173 158 105 53 23 419
Gerardo Camí Argentina 12 148 0.8× 182 1.1× 73 0.5× 115 1.1× 53 1.0× 34 449
Ping Ying China 7 240 1.3× 71 0.4× 76 0.5× 88 0.8× 41 0.8× 15 372
Caiqin Yang China 13 51 0.3× 258 1.5× 140 0.9× 67 0.6× 57 1.1× 38 441
Sulur G. Manjunatha India 10 198 1.0× 165 1.0× 162 1.0× 80 0.8× 87 1.6× 30 407
Xiaojie Sun China 6 46 0.2× 208 1.2× 139 0.9× 85 0.8× 32 0.6× 10 353
Duanxiu Li China 16 117 0.6× 359 2.1× 198 1.3× 70 0.7× 285 5.4× 31 628
Е. А. Дикусар Belarus 14 500 2.6× 123 0.7× 63 0.4× 104 1.0× 38 0.7× 166 685
Balvant Yadav India 11 64 0.3× 293 1.7× 170 1.1× 47 0.4× 19 0.4× 13 425

Countries citing papers authored by Sudhir Nambiar

Since Specialization
Citations

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

Fields of papers citing papers by Sudhir Nambiar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sudhir Nambiar

This figure shows the co-authorship network connecting the top 25 collaborators of Sudhir Nambiar. A scholar is included among the top collaborators of Sudhir Nambiar 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 Sudhir Nambiar. Sudhir Nambiar 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.
Koenig, Stefan G., Alina Borovika, Juan Colberg, et al.. (2019). A Green Chemistry Continuum for a Robust and Sustainable Active Pharmaceutical Ingredient Supply Chain. ACS Sustainable Chemistry & Engineering. 7(20). 16937–16951. 51 indexed citations
2.
Mittapalli, Sudhir, et al.. (2019). Novel solid form of prothioconazole and its crystallographic analysis. Journal of Molecular Structure. 1203. 127406–127406. 5 indexed citations
3.
Nambiar, Sudhir, et al.. (2016). The Development of a Manufacturing Route to an MCHr1 Antagonist. Organic Process Research & Development. 20(3). 675–682. 9 indexed citations
4.
Manjunatha, Sulur G., et al.. (2014). A novel synthetic approach to 4-acetamido-1-arylindazoles via Semmler–Wolff rearrangement of 1-aryl-6,7-dihydro-5H-indazol-4-one oxime. Tetrahedron Letters. 55(22). 3348–3350. 1 indexed citations
5.
Manjunatha, Sulur G., et al.. (2014). Semmler–Wolff aromatisation: a concise route for the synthesis of 5-amino-quinazolines and 4-amino-indoles. Tetrahedron Letters. 55(47). 6441–6446. 1 indexed citations
6.
Nambiar, Sudhir, et al.. (2014). Novel approach towards one pot stereospecific synthesis of carbohydrate derived substituted imidazolines. Tetrahedron Letters. 55(35). 4943–4947. 2 indexed citations
7.
Santhosh, U., K. Venkatesan, David S. Ennis, et al.. (2014). Development of a Safe, Scalable Process for the Preparation of an Oxaisoxazolidinone. Organic Process Research & Development. 18(12). 1802–1806. 1 indexed citations
8.
Shetty, Nandini P., Praveena Bhatt, Bhagyalakshmi Neelwarne, & Sudhir Nambiar. (2014). Inhibition of LDL oxidation and oxidized LDL-induced foam cell formation in RAW 264.7 cells show anti-atherogenic properties of a foliar methanol extract of Scoparia dulcis. Pharmacognosy Magazine. 10(38). 240–240. 10 indexed citations
9.
Ghosh, Avipsa, et al.. (2014). A Greener Approach for the Large-Scale Synthesis of 1,4,5-Trisubstituted Pyrazole, AZD8329. Organic Process Research & Development. 18(8). 947–951. 3 indexed citations
10.
Manjunatha, Sulur G., et al.. (2014). Exploiting the Differential Reactivities of Halogen Atoms: Development of a Scalable Route to IKK2 Inhibitor AZD3264. Organic Process Research & Development. 18(5). 646–651. 4 indexed citations
11.
Nambiar, Sudhir, et al.. (2013). Thermal studies of furosemide–caffeine binary system that forms a cocrystal. Journal of Thermal Analysis and Calorimetry. 115(3). 2261–2268. 19 indexed citations
12.
Manjunatha, Sulur G., et al.. (2012). Regio-selective synthesis of 1,2-aminoalcohols from epoxides and chlorohydrins. Tetrahedron Letters. 53(43). 5739–5741. 12 indexed citations
13.
Sanphui, Palash, et al.. (2012). Polymorphs and Cocrystals of Nalidixic Acid. Crystal Growth & Design. 12(10). 4963–4971. 27 indexed citations
14.
Goud, N. Rajesh, et al.. (2011). Novel Furosemide Cocrystals and Selection of High Solubility Drug Forms. Journal of Pharmaceutical Sciences. 101(2). 664–680. 145 indexed citations
15.
Rao, H. Surya Prakash, et al.. (2011). A mechanistic investigation of Biginelli reaction under base catalysis. Tetrahedron Letters. 52(28). 3605–3609. 28 indexed citations
16.
Nagarajan, N.S., et al.. (2011). Understanding of the mass spectrometric fragmentation pathways of a few potentially genotoxic haloaniline isomers in their protonated form by collision-induced dissociation. Journal of Pharmaceutical and Biomedical Analysis. 56(4). 721–727. 4 indexed citations
17.
Hanessian, Stephen, et al.. (1996). Synthesis of chemically and functionally diverse scaffolds from pentaerythritol. Canadian Journal of Chemistry. 74(9). 1731–1737. 15 indexed citations
18.
McAlister, D. B., Sudhir Nambiar, K. Grant Taylor, & R.J. Doyle. (1989). Glucosyltransferases of Streptococcus sobrinus C211 are both stimulated and inhibited by hydrogen peroxide. Oral Microbiology and Immunology. 4(3). 146–152. 3 indexed citations
19.
Nambiar, Sudhir, et al.. (1989). Dialdosides-(1,5) of glucose and galactose: synthesis, reactivity, and conformation. The Journal of Organic Chemistry. 54(10). 2300–2307. 10 indexed citations
20.
Nambiar, Sudhir, John F. Daeuble, Ronald J. Doyle, & K. Grant Taylor. (1989). Facile synthesis of silylated thioglycosides. Tetrahedron Letters. 30(17). 2179–2182. 28 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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