Richard Rampulla

988 total citations
17 papers, 282 citations indexed

About

Richard Rampulla is a scholar working on Organic Chemistry, Molecular Biology and Oncology. According to data from OpenAlex, Richard Rampulla has authored 17 papers receiving a total of 282 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 8 papers in Molecular Biology and 3 papers in Oncology. Recurrent topics in Richard Rampulla's work include Chemical Synthesis and Analysis (4 papers), Synthesis and Biological Evaluation (4 papers) and Synthesis of heterocyclic compounds (3 papers). Richard Rampulla is often cited by papers focused on Chemical Synthesis and Analysis (4 papers), Synthesis and Biological Evaluation (4 papers) and Synthesis of heterocyclic compounds (3 papers). Richard Rampulla collaborates with scholars based in United States, India and Germany. Richard Rampulla's co-authors include Ronald K. Russell, Jeffery B. Press, David Bright, Robert Falotico, Joan A. Keiser, Alfonso J. Tobia, James J. McNally, Arvind Mathur, Dieter H. Klaubert and Anuradha Gupta and has published in prestigious journals such as Journal of Medicinal Chemistry, The Journal of Organic Chemistry and Tetrahedron Letters.

In The Last Decade

Richard Rampulla

17 papers receiving 257 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Richard Rampulla United States 8 228 70 19 14 12 17 282
Jaimie K. Rueter United States 7 169 0.7× 130 1.9× 19 1.0× 32 2.3× 8 0.7× 10 221
Daniel Gardette France 13 317 1.4× 109 1.6× 21 1.1× 13 0.9× 16 1.3× 24 399
George T. Lee Switzerland 9 189 0.8× 55 0.8× 24 1.3× 16 1.1× 7 0.6× 13 232
Shahzad S. Rahman United Kingdom 11 271 1.2× 129 1.8× 25 1.3× 38 2.7× 13 1.1× 18 357
Walíd Fathalla Egypt 13 407 1.8× 134 1.9× 36 1.9× 10 0.7× 22 1.8× 55 473
Nikolai Yu. Kuznetsov Russia 11 212 0.9× 90 1.3× 27 1.4× 41 2.9× 15 1.3× 40 283
Alex Bridges United States 8 183 0.8× 106 1.5× 32 1.7× 8 0.6× 9 0.8× 13 291
Stefan Braese Germany 7 121 0.5× 74 1.1× 15 0.8× 13 0.9× 7 0.6× 73 166
Stéphane Raeppel France 10 185 0.8× 81 1.2× 31 1.6× 15 1.1× 5 0.4× 21 258
Tracy L. Deegan United States 8 200 0.9× 183 2.6× 19 1.0× 13 0.9× 7 0.6× 11 286

Countries citing papers authored by Richard Rampulla

Since Specialization
Citations

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

Fields of papers citing papers by Richard Rampulla

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Richard Rampulla

This figure shows the co-authorship network connecting the top 25 collaborators of Richard Rampulla. A scholar is included among the top collaborators of Richard Rampulla 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 Richard Rampulla. Richard Rampulla is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Vetrichelvan, Muthalagu, et al.. (2021). Solvent-specific, DAST-mediated intramolecular Friedel–Crafts reaction: access to dibenzoxepine-fused spirooxindoles. Organic & Biomolecular Chemistry. 19(8). 1760–1768. 2 indexed citations
2.
Nimje, Roshan Y., Muthalagu Vetrichelvan, Amol G. Dikundwar, et al.. (2021). Practical Synthesis of (3aR, 9bR)-8-Fluoro-7-(perfluoropropan-2-yl)-9b-(phenylsulfonyl)-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]indole: An Advanced Intermediate to Access the RORγt Inverse Agonist BMT-362265. Organic Process Research & Development. 25(4). 1001–1014. 7 indexed citations
3.
Nimje, Roshan Y., Richard Rampulla, Cullen L. Cavallaro, et al.. (2020). Synthesis of Differentially Protected Azatryptophan Analogs via Pd2(dba)3/XPhos Catalyzed Negishi Coupling of N-Ts Azaindole Halides with Zinc Derivative from Fmoc-Protected tert-Butyl (R)-2-Amino-3-iodopropanoate. The Journal of Organic Chemistry. 85(17). 11519–11530. 7 indexed citations
4.
Rampulla, Richard, et al.. (2020). Concise synthesis of chiral pyrazolo[4,3‐f] [1,4]oxazepines and pyrazolo[4,3‐f] [1,4]thiazepines bearing pyrazole unit. Journal of Heterocyclic Chemistry. 58(2). 558–568. 3 indexed citations
5.
Poudel, Yam B., Naidu S. Chowdari, Heng Cheng, et al.. (2020). Chemical Modification of Linkers Provides Stable Linker–Payloads for the Generation of Antibody–Drug Conjugates. ACS Medicinal Chemistry Letters. 11(11). 2190–2194. 26 indexed citations
6.
Oderinde, Martins S., James Kempson, Daniel Smith, et al.. (2019). Intramolecular [2+2] Cycloaddition of N‐Allylcinnamamines and N‐Allylcinnamamides by Visible‐Light Photocatalysis. European Journal of Organic Chemistry. 2020(1). 41–46. 22 indexed citations
7.
Sridharan, R., Makonen Belema, Nicholas A. Meanwell, et al.. (2019). Facile Access to 1,4-Disubstituted Pyrrolo[1,2-a]pyrazines from α-Aminoacetonitriles. Synthesis. 52(3). 441–449. 3 indexed citations
8.
Krishnamoorthy, Suresh, Pirama Nayagam Arunachalam, Ivar M. McDonald, et al.. (2018). Process Optimization for the Large-Scale Preparation of (2S,3aR,7aS)-tert-Butyl Hexahydro-2,5-methanopyrrolo[3,2-c]pyridine-1(4H)-carboxylate, an Intermediate for Nicotinic Acetylcholine Receptor Agonists. Organic Process Research & Development. 22(9). 1276–1281. 3 indexed citations
9.
10.
Gavai, Ashvinikumar V., et al.. (2016). Crystallization-Induced Dynamic Resolution toward the Synthesis of (S)-7-Amino-5H,7H-dibenzo[b,d]-azepin-6-one: An Important Scaffold for γ-Secretase Inhibitors. Organic Process Research & Development. 20(10). 1717–1720. 5 indexed citations
11.
Murray, William V., Alan Gill, Marylyn M. Addo, et al.. (1993). Substituted pyrrolidin-2-one biphenyltetrazoles as angiotensin II antagonists. Bioorganic & Medicinal Chemistry Letters. 3(2). 369–374. 12 indexed citations
12.
Russell, Ronald K., et al.. (1992). Preparation of N-1 Substituted Thieno[3,4-d]pyrimidine-2,4-diones. Synthetic Communications. 22(22). 3221–3227. 3 indexed citations
13.
Russell, Ronald K., et al.. (1992). The Synthesis of 2,3-Ring-Fused Analogues of 7-Fluoro-1-methyl-3-(methylsulfinyl)-4(1H)-quinolinone. Synthesis. 1992(8). 753–755. 5 indexed citations
14.
Combs, Donald W., Ronald K. Russell, Richard Rampulla, et al.. (1990). Design, synthesis and bronchodilatory activity of a series of quinazoline-3-oxides.. PubMed. 6(4). 241–54. 7 indexed citations
15.
Russell, Ronald K., et al.. (1990). Thiophene systems. 11. The synthesis of novel thieno[4,3,2‐de] tricyclic ring systems. Journal of Heterocyclic Chemistry. 27(6). 1761–1770. 13 indexed citations
16.
Russell, Ronald K., Jeffery B. Press, Richard Rampulla, et al.. (1988). Thiophene systems. 9. Thienopyrimidinedione derivatives as potential antihypertensive agents. Journal of Medicinal Chemistry. 31(9). 1786–1793. 147 indexed citations
17.
Rampulla, Richard & Ronald K. Russell. (1986). Selective Reduction of Nitroarylhydrazones by Catalytic Transfer Hydrogenation with Cyclohexene. Synthetic Communications. 16(10). 1229–1232. 4 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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