John A. Grosso

622 total citations
17 papers, 377 citations indexed

About

John A. Grosso is a scholar working on Organic Chemistry, Molecular Biology and Materials Chemistry. According to data from OpenAlex, John A. Grosso has authored 17 papers receiving a total of 377 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Organic Chemistry, 8 papers in Molecular Biology and 5 papers in Materials Chemistry. Recurrent topics in John A. Grosso's work include Phenothiazines and Benzothiazines Synthesis and Activities (4 papers), Synthesis and Characterization of Heterocyclic Compounds (3 papers) and Computational Drug Discovery Methods (3 papers). John A. Grosso is often cited by papers focused on Phenothiazines and Benzothiazines Synthesis and Activities (4 papers), Synthesis and Characterization of Heterocyclic Compounds (3 papers) and Computational Drug Discovery Methods (3 papers). John A. Grosso collaborates with scholars based in United States, Germany and United Kingdom. John A. Grosso's co-authors include David E. Nichols, Shawn X. Yin, Victor W. Rosso, Sandeep Modi, Sushil Srivastava, Thomas C. Sedergran, James H. Simpson, Michael Humora, Neal G. Anderson and Katerina Leftheris and has published in prestigious journals such as Journal of Medicinal Chemistry, The Journal of Organic Chemistry and Pharmaceutical Research.

In The Last Decade

John A. Grosso

17 papers receiving 357 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
John A. Grosso United States 10 261 96 46 37 36 17 377
Ádám Demeter Hungary 11 120 0.5× 71 0.7× 104 2.3× 79 2.1× 78 2.2× 30 333
Abdolmohammad Mehranpour Iran 11 244 0.9× 30 0.3× 95 2.1× 9 0.2× 37 1.0× 33 356
Brian M. Lynch Canada 14 490 1.9× 94 1.0× 62 1.3× 26 0.7× 76 2.1× 46 664
Tatyana A. Podrugina Russia 12 298 1.1× 41 0.4× 48 1.0× 20 0.5× 25 0.7× 38 408
Wayne D. Luke United States 7 144 0.6× 32 0.3× 58 1.3× 34 0.9× 51 1.4× 10 249
S. V. Zinchenko Russia 10 187 0.7× 60 0.6× 31 0.7× 33 0.9× 69 1.9× 53 317
Aabid A. Wani India 12 217 0.8× 88 0.9× 32 0.7× 14 0.4× 26 0.7× 27 330
Ashraf A. A. Abdel‐Fattah United States 14 364 1.4× 131 1.4× 19 0.4× 13 0.4× 45 1.3× 37 503
Giacomo Lo Moro Netherlands 11 198 0.8× 66 0.7× 23 0.5× 14 0.4× 46 1.3× 14 326
Michael M. Gilbert United States 10 410 1.6× 85 0.9× 40 0.9× 33 0.9× 41 1.1× 12 568

Countries citing papers authored by John A. Grosso

Since Specialization
Citations

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

Fields of papers citing papers by John A. Grosso

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John A. Grosso. 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 John A. Grosso. The network helps show where John A. Grosso may publish in the future.

Co-authorship network of co-authors of John A. Grosso

This figure shows the co-authorship network connecting the top 25 collaborators of John A. Grosso. A scholar is included among the top collaborators of John A. Grosso 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 John A. Grosso. John A. Grosso 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.
Pan, Duohai, et al.. (2013). Low level drug product API form analysis – Avalide tablet NIR quantitative method development and robustness challenges. Journal of Pharmaceutical and Biomedical Analysis. 89. 268–275. 33 indexed citations
2.
Chan, Steven H., et al.. (2012). A new perspective on the mechanical evaluation of granular material. Drug Development and Industrial Pharmacy. 39(7). 1126–1132. 8 indexed citations
3.
Yin, Shawn X. & John A. Grosso. (2009). ChemInform Abstract: Selecting and Controlling API Crystal Form for Pharmaceutical Development: Strategies and Processes. ChemInform. 40(11). 2 indexed citations
4.
Yin, Shawn X. & John A. Grosso. (2008). Selecting and controlling API crystal form for pharmaceutical development--strategies and processes.. PubMed. 11(6). 771–7. 8 indexed citations
5.
Huang, Yande, et al.. (2008). Identification of Critical Process Impurities and Their Impact on Process Research and Development. Organic Process Research & Development. 12(4). 632–636. 4 indexed citations
6.
Bhattacharya, Apurba, Vikram C. Purohit, Prashant P. Deshpande, et al.. (2007). An Alternate Route to 2-Amino-3-nitro-5-bromo-4-picoline: Regioselective Pyridine Synthesis via 2-Nitramino-picoline Intermediate. Organic Process Research & Development. 11(5). 885–888. 3 indexed citations
7.
8.
Bhattacharya, Apurba, et al.. (2006). Remarkable solvent effect in Barton–Zard pyrrole synthesis: application in an efficient one-step synthesis of pyrrole derivatives. Tetrahedron Letters. 47(31). 5481–5484. 26 indexed citations
9.
Bhattacharya, Apurba, Nitinchandra D. Patel, R. Erik Plata, et al.. (2006). An efficient electrophilic N-amination utilizing in situ generated chloramine under phase transfer conditions. Tetrahedron Letters. 47(30). 5341–5343. 7 indexed citations
10.
Hynes, John, Wendel W. Doubleday, Alaric J. Dyckman, et al.. (2004). N-Amination of Pyrrole and Indole Heterocycles with Monochloramine (NH2Cl). The Journal of Organic Chemistry. 69(4). 1368–1371. 58 indexed citations
11.
Li, Jun, et al.. (2003). Selective removal of a benzyl protecting group in the presence of an aryl chloride under gaseous and transfer hydrogenolysis conditions. Tetrahedron Letters. 44(21). 4041–4043. 11 indexed citations
12.
Wang, Jianji, Robert P. Discordia, Gerard A. Crispino, et al.. (2003). A mild and efficient synthesis of 4-aryl-quinolin-2(1H)-ones via a tandem amidation/Knoevenagel condensation of 2-amino-benzophenones with esters or lactones. Tetrahedron Letters. 44(22). 4271–4273. 26 indexed citations
13.
Yang, Ming, et al.. (2003). A Practical Pilot-Scale Synthesis of 4-Vinyl-2,3-dihydrobenzofuran Using Imidate Ester Chemistry and Phase-Transfer Catalysis. Organic Process Research & Development. 7(4). 547–550. 11 indexed citations
14.
Rosso, Victor W., John A. Grosso, Sandeep Modi, et al.. (1997). Removal of Palladium from Organic Reaction Mixtures by Trimercaptotriazine. Organic Process Research & Development. 1(4). 311–314. 104 indexed citations
15.
Thakur, Ajit B., et al.. (1993). Mechanism and Kinetics of Metal Ion-Mediated Degradation of Fosinopril Sodium. Pharmaceutical Research. 10(6). 800–809. 20 indexed citations
16.
Grosso, John A., David E. Nichols, Jai D. Kohli, & Dana Glock. (1982). Synthesis of 2-(alkylamino)-5,6- and -6,7-dihydroxy-3,4-dihydroquinazolines and evaluation as potential dopamine agonists. Journal of Medicinal Chemistry. 25(6). 703–708. 32 indexed citations
17.
Grosso, John A., et al.. (1980). Synthesis and adrenergic blocking effects of 2-(alkylamino)-3,4-dihydroquinazolines. Journal of Medicinal Chemistry. 23(11). 1261–1264. 23 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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