Christopher G. Hamaker

1.0k total citations
49 papers, 854 citations indexed

About

Christopher G. Hamaker is a scholar working on Organic Chemistry, Oncology and Inorganic Chemistry. According to data from OpenAlex, Christopher G. Hamaker has authored 49 papers receiving a total of 854 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Organic Chemistry, 17 papers in Oncology and 17 papers in Inorganic Chemistry. Recurrent topics in Christopher G. Hamaker's work include Metal complexes synthesis and properties (17 papers), Crystal structures of chemical compounds (10 papers) and Asymmetric Synthesis and Catalysis (9 papers). Christopher G. Hamaker is often cited by papers focused on Metal complexes synthesis and properties (17 papers), Crystal structures of chemical compounds (10 papers) and Asymmetric Synthesis and Catalysis (9 papers). Christopher G. Hamaker collaborates with scholars based in United States, Puerto Rico and France. Christopher G. Hamaker's co-authors include L. Keith Woo, Jean‐Pierre Djukic, Thomas Kodadek, Gholam A. Mirafzal, Shawn R. Hitchcock, Daniel Smith, T. Andrew Mitchell, M.P. Weberski, John R. Goodell and Céline Dablemont and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Communications and Ecology Letters.

In The Last Decade

Christopher G. Hamaker

48 papers receiving 832 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher G. Hamaker United States 16 614 276 160 123 100 49 854
Bianca R. Sculimbrene United States 14 594 1.0× 152 0.6× 148 0.9× 26 0.2× 475 4.8× 19 871
Vesna B. Medaković Serbia 12 179 0.3× 209 0.8× 122 0.8× 115 0.9× 97 1.0× 21 577
Xuefei Zhao China 14 239 0.4× 89 0.3× 275 1.7× 19 0.2× 110 1.1× 39 785
Kohei Inomata Japan 18 595 1.0× 49 0.2× 49 0.3× 22 0.2× 124 1.2× 43 781
T.S. Griffin United States 8 239 0.4× 63 0.2× 164 1.0× 29 0.2× 162 1.6× 14 658
R. Fernando Martínez United Kingdom 16 436 0.7× 59 0.2× 108 0.7× 27 0.2× 229 2.3× 37 661
César Raposo Spain 17 361 0.6× 85 0.3× 162 1.0× 18 0.1× 279 2.8× 57 793
Mauro I. Ciglic United States 13 324 0.5× 164 0.6× 68 0.4× 21 0.2× 153 1.5× 28 541
Xueyan Zhang China 15 254 0.4× 62 0.2× 92 0.6× 8 0.1× 227 2.3× 48 561
Jakka Kavitha India 13 301 0.5× 52 0.2× 328 2.0× 51 0.4× 110 1.1× 30 802

Countries citing papers authored by Christopher G. Hamaker

Since Specialization
Citations

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

Fields of papers citing papers by Christopher G. Hamaker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher G. Hamaker. 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 Christopher G. Hamaker. The network helps show where Christopher G. Hamaker may publish in the future.

Co-authorship network of co-authors of Christopher G. Hamaker

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher G. Hamaker. A scholar is included among the top collaborators of Christopher G. Hamaker 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 Christopher G. Hamaker. Christopher G. Hamaker 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.
2.
Hamaker, Christopher G., et al.. (2024). Synthesis and Crystal Structure Analysis of Some Aromatic Imines of Syringaldehyde. Crystals. 14(1). 99–99. 1 indexed citations
3.
Jones, Marjorie A., et al.. (2020). Ruthenium(III) complexes with imidazole ligands that modulate the aggregation of the amyloid-β peptide via hydrophobic interactions. Journal of Inorganic Biochemistry. 214. 111303–111303. 19 indexed citations
4.
Hamaker, Christopher G., et al.. (2017). Sulfonamides as Inhibitors of Leishmania – Potential New Treatments for Leishmaniasis. Anti-Infective Agents. 15(1). 57–62. 4 indexed citations
5.
6.
Bruce, J. Malcolm, et al.. (2016). syn-Diastereoselective glycolate aldol addition reactions of an N(3)-(p-methoxyphenoxy)acetyloxazolidine-2-thione. Tetrahedron Asymmetry. 28(1). 98–104. 2 indexed citations
7.
Avdeev, Maxim, et al.. (2015). Structure, stability, and photoluminescence in the anti-perovskites Na3W1−Mo O4F (0≤x≤1). Journal of Solid State Chemistry. 230. 279–286. 9 indexed citations
8.
Hamaker, Christopher G., et al.. (2014). Investigation of oxidopyrylium–alkene [5+2] cycloaddition conjugate addition cascade (C3) sequences. Chemical Communications. 50(65). 9130–9133. 21 indexed citations
9.
Weddle, Carie B., Sandra Steiger, Christopher G. Hamaker, et al.. (2012). Cuticular hydrocarbons as a basis for chemosensory self‐referencing in crickets: a potentially universal mechanism facilitating polyandry in insects. Ecology Letters. 16(3). 346–353. 45 indexed citations
10.
Hamaker, Christopher G., et al.. (2010). Aromatic motifs in the design of Ephedra ligands for application in the asymmetric addition of diethylzinc to aldehydes and diphenylphosphinoylimines. Tetrahedron Asymmetry. 21(5). 549–557. 10 indexed citations
11.
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Jin, Guang, et al.. (2008). Use of a whole-cell biocatalyst to produce biodiesel in a water-containing system. Journal of Environmental Science and Health Part A. 44(1). 21–28. 10 indexed citations
13.
Chávez-Gil, Tulio, David L. Cedeño, Christopher G. Hamaker, M. Cristina Vega, & Jéssica Rodríguez. (2008). Synthesis, characterization, and crystal structure of [Cu{(3,5-Ph2Pz)2BH2}2]0: Evidence of a B–H–Cu agostic interaction. Journal of Molecular Structure. 888(1-3). 168–172. 10 indexed citations
14.
Hamaker, Christopher G., et al.. (2008). Salicylaldehyde based oxazolidines as catalysts for the asymmetric addition of diethylzinc to aldehydes. Journal of Heterocyclic Chemistry. 45(3). 873–878. 6 indexed citations
15.
Jin, Guang, et al.. (2008). Producing biodiesel using whole-cell biocatalysts in separate hydrolysis and methanolysis reactions. Journal of Environmental Science and Health Part A. 43(6). 589–595. 10 indexed citations
16.
17.
Hamaker, Christopher G., et al.. (2006). 3-Acetyl-7-(diethylamino)coumarin. Acta Crystallographica Section E Structure Reports Online. 62(5). o2072–o2074. 3 indexed citations
18.
Hamaker, Christopher G., et al.. (2006). Synthesis and crystal structures of the bis-Schiff bases of 2-(methylthio)aniline with isophthaldehyde, terephthaldehyde, and para-diacetylbenzene. Journal of Chemical Crystallography. 36(11). 735–742. 18 indexed citations
19.
Weberski, M.P., C.C. McLauchlan, & Christopher G. Hamaker. (2005). Synthesis and X-ray structural characterization of M(3,5-tBu2-salophen) (M=Cu, VO). Polyhedron. 25(1). 119–123. 24 indexed citations
20.
Hamaker, Christopher G., et al.. (2005). 3-Methoxy-N-[2-(methylsulfanyl)phenyl]salicylaldimine. Acta Crystallographica Section E Structure Reports Online. 62(1). o68–o69. 3 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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