Ashton T. Hamme

1.0k total citations
34 papers, 836 citations indexed

About

Ashton T. Hamme is a scholar working on Organic Chemistry, Molecular Biology and Biomedical Engineering. According to data from OpenAlex, Ashton T. Hamme has authored 34 papers receiving a total of 836 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Organic Chemistry, 14 papers in Molecular Biology and 8 papers in Biomedical Engineering. Recurrent topics in Ashton T. Hamme's work include Synthesis and Catalytic Reactions (9 papers), Synthesis and Biological Evaluation (9 papers) and Click Chemistry and Applications (8 papers). Ashton T. Hamme is often cited by papers focused on Synthesis and Catalytic Reactions (9 papers), Synthesis and Biological Evaluation (9 papers) and Click Chemistry and Applications (8 papers). Ashton T. Hamme collaborates with scholars based in United States. Ashton T. Hamme's co-authors include Sureshbabu Dadiboyena, E. Valente, Paresh Chandra Ray, Yunfeng Lin, Jianping Xu, Rajashekhar Kanchanapally, Bhanu Priya Viraka Nellore, Sudarson Sekhar Sinha, Avijit Pramanik and Dhiraj K. Sardar and has published in prestigious journals such as Journal of the American Chemical Society, ACS Applied Materials & Interfaces and The Journal of Organic Chemistry.

In The Last Decade

Ashton T. Hamme

34 papers receiving 816 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ashton T. Hamme United States 18 403 282 257 141 79 34 836
Srinivas Banala Germany 18 258 0.6× 278 1.0× 312 1.2× 254 1.8× 18 0.2× 45 931
Mayreli Ortiz Spain 18 178 0.4× 246 0.9× 500 1.9× 210 1.5× 91 1.2× 63 972
Wilker Caetano Brazil 17 150 0.4× 261 0.9× 195 0.8× 257 1.8× 14 0.2× 30 670
I. Ya. Dubey Ukraine 16 169 0.4× 72 0.3× 378 1.5× 162 1.1× 52 0.7× 71 700
Ruggero Dondi United Kingdom 11 184 0.5× 107 0.4× 178 0.7× 139 1.0× 35 0.4× 16 483
Karol Krzymiński Poland 14 282 0.7× 107 0.4× 163 0.6× 154 1.1× 22 0.3× 69 587
Xuefeng Li China 21 788 2.0× 171 0.6× 209 0.8× 193 1.4× 19 0.2× 62 1.2k
Thomas H. Kalantar United States 10 333 0.8× 58 0.2× 184 0.7× 105 0.7× 13 0.2× 20 565
Pat Forgione Canada 20 1.3k 3.2× 143 0.5× 170 0.7× 117 0.8× 14 0.2× 68 1.6k
Deepak K. Sharma India 20 510 1.3× 104 0.4× 345 1.3× 164 1.2× 24 0.3× 96 1.1k

Countries citing papers authored by Ashton T. Hamme

Since Specialization
Citations

This map shows the geographic impact of Ashton T. Hamme'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 Ashton T. Hamme with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ashton T. Hamme more than expected).

Fields of papers citing papers by Ashton T. Hamme

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ashton T. Hamme. 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 Ashton T. Hamme. The network helps show where Ashton T. Hamme may publish in the future.

Co-authorship network of co-authors of Ashton T. Hamme

This figure shows the co-authorship network connecting the top 25 collaborators of Ashton T. Hamme. A scholar is included among the top collaborators of Ashton T. Hamme 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 Ashton T. Hamme. Ashton T. Hamme 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.
Hamme, Ashton T., et al.. (2022). Bromo-lactamization of isoxazole via neighboring group participation: toward spiro-isoxazoline γ- and δ-lactams. RSC Advances. 12(16). 9628–9636. 2 indexed citations
2.
Mitra, Dipanwita, et al.. (2020). Synthesis and biological evaluation of fluoro-substituted spiro-isoxazolines as potential anti-viral and anti-cancer agents. RSC Advances. 10(50). 30223–30237. 22 indexed citations
3.
Hamme, Ashton T., et al.. (2015). Divergent and Concise Syntheses of Spiroisoxazolines: First Total Synthesis of 11‐Deoxyfistularin‐3. European Journal of Organic Chemistry. 2015(23). 5159–5166. 14 indexed citations
4.
Nellore, Bhanu Priya Viraka, Rajashekhar Kanchanapally, Avijit Pramanik, et al.. (2015). Aptamer-Conjugated Graphene Oxide Membranes for Highly Efficient Capture and Accurate Identification of Multiple Types of Circulating Tumor Cells. Bioconjugate Chemistry. 26(2). 235–242. 94 indexed citations
5.
Sitole, Lungile, et al.. (2015). Synthesis and investigation of novel spiro-isoxazolines as anti-cancer agents. Tetrahedron Letters. 56(14). 1794–1797. 31 indexed citations
6.
Dadiboyena, Sureshbabu, E. Valente, & Ashton T. Hamme. (2014). Synthesis and tautomerism of spiro-pyrazolines. Tetrahedron Letters. 55(14). 2208–2211. 16 indexed citations
7.
Dadiboyena, Sureshbabu & Ashton T. Hamme. (2013). Environmentally Benign Lewis Acid Promoted [2+3] Dipolar Cycloaddition Reactions of Nitrile Imines with Alkenes in Water. European Journal of Organic Chemistry. 2013(33). 7567–7574. 19 indexed citations
9.
Dadiboyena, Sureshbabu & Ashton T. Hamme. (2012). Synthesis of Celecoxib and Structural Analogs- A Review. Current Organic Chemistry. 16(11). 1390–1407. 18 indexed citations
10.
Dadiboyena, Sureshbabu & Ashton T. Hamme. (2011). One pot spiropyrazoline synthesis via intramolecular cyclization/methylation. Tetrahedron Letters. 52(20). 2536–2539. 19 indexed citations
11.
Dadiboyena, Sureshbabu, E. Valente, & Ashton T. Hamme. (2010). Synthesis of novel pyrazoles via [2+3]-dipolar cycloaddition using alkyne surrogates. Tetrahedron Letters. 51(9). 1341–1343. 43 indexed citations
12.
Xu, Jianping, et al.. (2009). Construction of novel spiroisoxazolines via intramolecular cyclization/methylation. Tetrahedron Letters. 50(39). 5516–5519. 9 indexed citations
13.
Valente, E., et al.. (2008). Oxonium ion-mediated synthesis of 4-substituted spiro-isoxazolines. Tetrahedron Letters. 50(5). 533–535. 16 indexed citations
14.
Dadiboyena, Sureshbabu, E. Valente, & Ashton T. Hamme. (2008). A novel synthesis of 1,3,5-trisubstituted pyrazoles through a spiro-pyrazoline intermediate via a tandem 1,3-dipolar cycloaddition/elimination. Tetrahedron Letters. 50(3). 291–294. 47 indexed citations
15.
Dadiboyena, Sureshbabu, Jianping Xu, & Ashton T. Hamme. (2007). Isoxazoles from 1,1-disubstituted bromoalkenes. Tetrahedron Letters. 48(7). 1295–1298. 50 indexed citations
16.
Rasulev, Bakhtiyor, Andrey A. Toropov, Ashton T. Hamme, & Jerzy Leszczyński. (2007). Multiple Linear Regression Analysis and Optimal Descriptors: Predicting the Cholesteryl Ester Transfer Protein Inhibition Activity. QSAR & Combinatorial Science. 27(5). 595–606. 14 indexed citations
17.
19.
Paquette, Leo A., et al.. (1997). Sensitivity of Substitution to the Extent of Self-Immolative Chirality Transfer during Reaction Cascades Originating from Squarate Esters. The Journal of Organic Chemistry. 62(6). 1730–1736. 14 indexed citations
20.

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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