Eugene Farkas

789 total citations · 1 hit paper
28 papers, 645 citations indexed

About

Eugene Farkas is a scholar working on Organic Chemistry, Molecular Biology and Genetics. According to data from OpenAlex, Eugene Farkas has authored 28 papers receiving a total of 645 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Organic Chemistry, 14 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Eugene Farkas's work include Steroid Chemistry and Biochemistry (10 papers), Asymmetric Synthesis and Catalysis (4 papers) and Estrogen and related hormone effects (4 papers). Eugene Farkas is often cited by papers focused on Steroid Chemistry and Biochemistry (10 papers), Asymmetric Synthesis and Catalysis (4 papers) and Estrogen and related hormone effects (4 papers). Eugene Farkas collaborates with scholars based in United States and Hungary. Eugene Farkas's co-authors include Ernest Wenkert, Banavara L. Mylari, David M. Doddrell, Paul V. Demarco, Calvin L. Stevens, Bernard T. Gillis, Carl Djerassi, John M. Owen, W. H. W. LUNN and G. H. THOMAS and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Medicinal Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Eugene Farkas

27 papers receiving 578 citations

Hit Papers

Pyridine-induced solvent ... 1968 2026 1987 2006 1968 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eugene Farkas United States 12 292 265 100 86 66 28 645
Ewart R. H. Jones United States 14 312 1.1× 176 0.7× 88 0.9× 70 0.8× 30 0.5× 79 588
N. L. Wendler United States 18 561 1.9× 603 2.3× 63 0.6× 165 1.9× 98 1.5× 103 1.1k
Masanao Matsui Japan 11 271 0.9× 242 0.9× 48 0.5× 75 0.9× 27 0.4× 117 547
Thomas Money Canada 18 332 1.1× 541 2.0× 103 1.0× 124 1.4× 102 1.5× 70 870
U. R. Nayak India 16 408 1.4× 363 1.4× 102 1.0× 229 2.7× 44 0.7× 56 866
Robin B. Boar United Kingdom 14 403 1.4× 255 1.0× 61 0.6× 85 1.0× 22 0.3× 47 687
A. J. Lemin United States 13 309 1.1× 223 0.8× 129 1.3× 51 0.6× 17 0.3× 25 629
T. G. Halsall United Kingdom 18 671 2.3× 429 1.6× 175 1.8× 225 2.6× 66 1.0× 93 1.3k
D. E. A. Rivett South Africa 15 209 0.7× 273 1.0× 126 1.3× 63 0.7× 59 0.9× 44 563
Ek. Weiss Switzerland 17 506 1.7× 169 0.6× 195 1.9× 82 1.0× 31 0.5× 53 828

Countries citing papers authored by Eugene Farkas

Since Specialization
Citations

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

Fields of papers citing papers by Eugene Farkas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eugene Farkas

This figure shows the co-authorship network connecting the top 25 collaborators of Eugene Farkas. A scholar is included among the top collaborators of Eugene Farkas 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 Eugene Farkas. Eugene Farkas 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.
Misner, Jerry W., Michael A. Staszak, Christopher W. Doecke, et al.. (2000). Enantioselective Syntheses of 1-Carbacephalosporins from Chemoenzymically Derived β-Hydroxy-α-Amino Acids: Applications to the Total Synthesis of Carbacephem Antibiotic Loracarbef. Tetrahedron. 56(31). 5667–5677. 21 indexed citations
2.
Paquette, Leo A., Eugene Farkas, & Robert A. Galemmo. (1981). 4,7,7-Trimethyl-cis-bicyclo[3.3.0]oct-3-en-2-one. Potentially useful synthon for triquinane natural products. The Journal of Organic Chemistry. 46(26). 5434–5436. 2 indexed citations
3.
Farkas, Eugene, et al.. (1971). 17α-ethynyl-17β-hydroxy-10α-estr-4-en-3-one. Steroids. 17(1-5). 317–322. 1 indexed citations
4.
Farkas, Eugene & Nicholas J. Bach. (1971). Catalytic dehydrogenation of estr-4-en-3-ones. The Journal of Organic Chemistry. 36(18). 2715–2717. 2 indexed citations
5.
Debono, Manuel, Eugene Farkas, Robert M. Molloy, & John M. Owen. (1969). Chemistry of 10.alpha.-estr-4-en-17.beta.-ol-3-one and selected transformation products. The Journal of Organic Chemistry. 34(5). 1447–1450. 8 indexed citations
6.
LUNN, W. H. W. & Eugene Farkas. (1968). The adamantyl carbonium ion as a dehydrogenating agent, its reactions with estrone. Tetrahedron. 24(23). 6773–6776. 13 indexed citations
7.
Farkas, Eugene, John M. Owen, Manuel Debono, Robert M. Molloy, & Max M. Marsh. (1966). The preparatiom and chemistsy of the 10α-estra-4- en-3-ones. Tetrahedron Letters. 7(10). 1023–1027. 5 indexed citations
8.
Harrison, Ian T., et al.. (1964). Steroids CCLXX. Biologically-active labile ethers II. A new group of potent orally-active estrogens. Steroids. 4(3). 423–432. 7 indexed citations
9.
Farkas, Eugene, et al.. (1964). Steroidal Carbamic Acid γ-Lactones. Journal of Medicinal Chemistry. 7(6). 739–741. 7 indexed citations
10.
Farkas, Eugene, et al.. (1958). Notes: Preparation of a New Class of Steroids with Unnatural Configuration. The 19-Nor-5α, 10α Series. The Journal of Organic Chemistry. 23(9). 1404–1405. 10 indexed citations
11.
Farkas, Eugene, et al.. (1958). PREPARATION OF 5β,10β-ESTRANE-3,17-DIONE AND RELATED DERIVATIVES AND PROOF OF THEIR CONFIGURATION. Journal of the American Chemical Society. 80(4). 1008–1009. 12 indexed citations
12.
Lavagnino, E. R., et al.. (1957). New Total Synthesis of dl-Alloyohimbane and dl-Epialloyohimbane and their 11-Methoxy Derivatives. Journal of the American Chemical Society. 79(14). 3770–3772. 6 indexed citations
13.
Farkas, Eugene, et al.. (1957). Notes - Preparation of 3-Dehydroeserpic Acid Lactone and Its Conversion to Reserpic Acid Lactone. The Journal of Organic Chemistry. 22(10). 1261–1263. 2 indexed citations
14.
Djerassi, Carl, et al.. (1955). Terpenoids. XVII.1 The Cactus Triterpenes Thurberogenin and Stellatogenin2. Journal of the American Chemical Society. 77(20). 5330–5336. 22 indexed citations
15.
Farkas, Eugene, et al.. (1955). 17β-Methyl-Δ5-androstene-3β-ol. Journal of the American Chemical Society. 77(24). 6685–6685. 1 indexed citations
16.
Cope, Arthur C. & Eugene Farkas. (1954). CLEAVAGE OF CARBON-SULFUR BONDS BY CATALYTIC HYDROGENATION. The Journal of Organic Chemistry. 19(3). 385–390. 5 indexed citations
17.
Djerassi, Carl, et al.. (1954). Terpenoids. VI.1 Dumortierigenin, a New Triterpene Lactone from the Cactus Lemaireocereus dumortieri2. Journal of the American Chemical Society. 76(11). 2969–2973. 14 indexed citations
18.
Stevens, Calvin L. & Eugene Farkas. (1953). Halogen Migration in the Friedel—Crafts Acylation of Olefins1. Journal of the American Chemical Society. 75(14). 3306–3308. 3 indexed citations
19.
Stevens, Calvin L. & Eugene Farkas. (1952). The Formation of 1-Phenylcyclohexanecarboxylic Acid from α-Halocyclohexyl Phenyl Ketones. Journal of the American Chemical Society. 74(21). 5352–5355. 10 indexed citations
20.
Stevens, Calvin L. & Eugene Farkas. (1952). Epoxyethers. II. The Epoxyether from α-Halocyclohexyl Phenyl Ketone1. Journal of the American Chemical Society. 74(3). 618–620. 14 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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