Gabor Lukacs

2.1k total citations
116 papers, 1.5k citations indexed

About

Gabor Lukacs is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Gabor Lukacs has authored 116 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Organic Chemistry, 41 papers in Molecular Biology and 31 papers in Spectroscopy. Recurrent topics in Gabor Lukacs's work include Carbohydrate Chemistry and Synthesis (45 papers), Microbial Natural Products and Biosynthesis (23 papers) and Synthetic Organic Chemistry Methods (16 papers). Gabor Lukacs is often cited by papers focused on Carbohydrate Chemistry and Synthesis (45 papers), Microbial Natural Products and Biosynthesis (23 papers) and Synthetic Organic Chemistry Methods (16 papers). Gabor Lukacs collaborates with scholars based in France, Japan and Hungary. Gabor Lukacs's co-authors include Alain Olesker, Satoshi Ōmura, Ton That Thang, András Neszmélyi, Akira Nakagawa, François Piriou, J. Cristobal López, Stephan D. Géro, Sergio Castillón and Akira Nakagawa and has published in prestigious journals such as Journal of the American Chemical Society, Biochemistry and The Journal of Organic Chemistry.

In The Last Decade

Gabor Lukacs

115 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gabor Lukacs France 22 910 774 420 144 137 116 1.5k
Thomas L. Shih United States 13 1.4k 1.5× 605 0.8× 281 0.7× 127 0.9× 201 1.5× 26 1.8k
Glenn A. Berchtold United States 26 962 1.1× 682 0.9× 176 0.4× 140 1.0× 57 0.4× 85 1.7k
R. H. WIGHTMAN United Kingdom 26 1.5k 1.6× 1.1k 1.4× 163 0.4× 117 0.8× 87 0.6× 116 2.0k
Richard H. Mueller United States 21 1.6k 1.8× 626 0.8× 153 0.4× 131 0.9× 128 0.9× 44 2.0k
John K. Snyder United States 31 1.8k 1.9× 1.0k 1.4× 281 0.7× 219 1.5× 134 1.0× 118 2.8k
Tetsuo Suami Japan 25 2.1k 2.3× 1.3k 1.7× 398 0.9× 151 1.0× 337 2.5× 236 2.6k
Tammo Winkler Switzerland 23 1.2k 1.3× 718 0.9× 225 0.5× 173 1.2× 50 0.4× 129 2.0k
Milton L. Hammond United States 28 1.1k 1.2× 666 0.9× 499 1.2× 90 0.6× 51 0.4× 73 2.3k
S. A. MIZSAK United States 23 1.1k 1.2× 983 1.3× 611 1.5× 94 0.7× 300 2.2× 92 2.0k
Richard B. Herbert United Kingdom 18 487 0.5× 610 0.8× 302 0.7× 70 0.5× 111 0.8× 105 1.2k

Countries citing papers authored by Gabor Lukacs

Since Specialization
Citations

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

Fields of papers citing papers by Gabor Lukacs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gabor Lukacs

This figure shows the co-authorship network connecting the top 25 collaborators of Gabor Lukacs. A scholar is included among the top collaborators of Gabor Lukacs 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 Gabor Lukacs. Gabor Lukacs 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.
Saha, Krishnendu, et al.. (2018). Lean Six-Sigma: the means to healing an ailing NHS?. International Journal of Quality & Reliability Management. 35(9). 1976–1988. 4 indexed citations
2.
Grandjean, Cyrille & Gabor Lukacs. (1996). Preparation and In Vitro Antibacterial Activity of 9-O-Glycosyloxime Derivatives of Erythromycin A, a New Class of Macrolide Antibiotics.. The Journal of Antibiotics. 49(10). 1036–1043. 5 indexed citations
3.
Grandjean, Cyrille & Gabor Lukacs. (1996). SN2Displacement of Carbohydrate Triflates by 9-Oximes of Erythromycin A and Of a Tylosin Derivative. Journal of Carbohydrate Chemistry. 15(7). 831–855. 4 indexed citations
4.
Lukacs, Gabor, et al.. (1995). A convergent carbohydrate approach to the synthesis of taxol. Part 2. Ring C subunit. Tetrahedron Letters. 36(14). 2465–2468. 9 indexed citations
5.
Ghini, Alberto A., et al.. (1990). Intramolecular Diels-Alder reactions on pyranose trienes. Stereoselective access to bis-annulated pyranosides.. Tetrahedron Letters. 31(16). 2301–2304. 12 indexed citations
6.
Olesker, Alain, et al.. (1989). Synthesis and biological activity of the two isomeric 2'-C-methyl daunomycins.. The Journal of Antibiotics. 42(9). 1393–1397. 1 indexed citations
7.
8.
Olesker, Alain, et al.. (1989). Synthesis and antibacterial activity of 9-O-((2-methoxyethoxy)methyl)-oximes of tylosin and demycarosyltylosin.. The Journal of Antibiotics. 42(9). 1443–1445. 3 indexed citations
9.
Alves, Ricardo José, et al.. (1988). Synthesis of a Chiral Hexane-1,6-Dinitrile from D-Glucose. Journal of Carbohydrate Chemistry. 7(3). 655–659.
10.
Bliard, Christophe, Francisca Cabrera‐Escribano, Gabor Lukacs, Alain Olesker, & Pierre Sarda. (1987). Synthesis of C-2″β- and C-2″α-fluoro avermectin B1a. Journal of the Chemical Society Chemical Communications. 368–370. 14 indexed citations
11.
Costa, Sônia Soares, Alain Olesker, Ton That Thang, & Gabor Lukacs. (1984). Synthesis of two fragments of the 14-membered macrolide antibiotic oleandomycin from D-glucose. The Journal of Organic Chemistry. 49(13). 2338–2341. 6 indexed citations
12.
Olesker, Alain, et al.. (1982). A route from d-galactose to the aggregation pheromone component (-)-α-multistriatin. Carbohydrate Research. 110(1). 159–164. 7 indexed citations
13.
Lukacs, Gabor & András Neszmélyi. (1981). Natural abundance13C–13C coupling constants in a steroid. Journal of the Chemical Society Chemical Communications. 1275–1277. 1 indexed citations
14.
Neszmélyi, András, Satoshi Ōmura, Ton That Thang, & Gabor Lukacs. (1977). A carbon - 13 spin-lattice relaxation time study of 14-membered macrolide antibiotics(1).. Tetrahedron Letters. 18(8). 725–728. 3 indexed citations
15.
Ōmura, Satoshi, et al.. (1976). Studies on carboxylic acid metabolism in a macrolide-producing microorganism using carbon-13 magnetic resonance. Bioorganic Chemistry. 5(4). 451–454. 13 indexed citations
16.
Polonsky, Judith, et al.. (1975). Application du couplage13C-13C a la determination de l'origine biogenetique des substituants en C-4 des virescenols A et B. Tetrahedron Letters. 16(7). 481–484. 3 indexed citations
17.
18.
Tori, Kazuo, et al.. (1975). Carbon-13 Nmr spectra of steroidal A-ring episulfides. Tetrahedron Letters. 16(2). 135–138. 4 indexed citations
19.
Ōmura, Satoshi, Akira Nakagawa, Hideo Takeshima, et al.. (1975). A 3C nuclear magnetic resonance study of the biosynthesis of the 16-membered macrolide antibiotic tylosin. Tetrahedron Letters. 16(50). 4503–4506. 27 indexed citations
20.
Chachaty, C., et al.. (1974). Effets de substituants sur la relaxation spin réseau du 13C dans les chaines aliphatiques. application aux prostaglandines. Journal de Chimie Physique. 71. 487–495. 2 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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