E. GACS‐BAITZ

415 total citations
21 papers, 358 citations indexed

About

E. GACS‐BAITZ is a scholar working on Organic Chemistry, Spectroscopy and Molecular Biology. According to data from OpenAlex, E. GACS‐BAITZ has authored 21 papers receiving a total of 358 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Organic Chemistry, 10 papers in Spectroscopy and 4 papers in Molecular Biology. Recurrent topics in E. GACS‐BAITZ's work include Molecular spectroscopy and chirality (5 papers), Liquid Crystal Research Advancements (4 papers) and Analytical Chemistry and Chromatography (3 papers). E. GACS‐BAITZ is often cited by papers focused on Molecular spectroscopy and chirality (5 papers), Liquid Crystal Research Advancements (4 papers) and Analytical Chemistry and Chromatography (3 papers). E. GACS‐BAITZ collaborates with scholars based in Hungary, Italy and France. E. GACS‐BAITZ's co-authors include Francesco De Simone, Rita Patrizia Aquino, Giuliano Delle Monache, Bruno Botta, F. F. Vincieri, Cosimo Pìzza, Giovanni Zappia, Domenico Misiti, Laura Nevola and Katalin Fodor‐Csorba and has published in prestigious journals such as Phytochemistry, European Journal of Medicinal Chemistry and Journal of Natural Products.

In The Last Decade

E. GACS‐BAITZ

21 papers receiving 342 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. GACS‐BAITZ Hungary 10 169 136 64 62 58 21 358
Ching‐Pong Mak Austria 11 301 1.8× 133 1.0× 40 0.6× 12 0.2× 34 0.6× 24 413
J. Siva Prasad India 12 309 1.8× 145 1.1× 33 0.5× 44 0.7× 16 0.3× 32 574
R.J. Sowden United Kingdom 8 65 0.4× 194 1.4× 28 0.4× 39 0.6× 162 2.8× 10 377
Marı́a Valpuesta Spain 13 280 1.7× 114 0.8× 18 0.3× 18 0.3× 58 1.0× 40 422
E. P. SEREBRYAKOV Russia 12 309 1.8× 176 1.3× 46 0.7× 7 0.1× 13 0.2× 88 520
Lars Andernach Germany 11 150 0.9× 104 0.8× 54 0.8× 13 0.2× 11 0.2× 24 326
G. Snatzke Germany 9 200 1.2× 170 1.3× 117 1.8× 13 0.2× 18 0.3× 27 430
Marian Olejnik Poland 10 94 0.6× 110 0.8× 35 0.5× 34 0.5× 52 0.9× 17 350
Nelson R. Easton United States 12 261 1.5× 142 1.0× 47 0.7× 8 0.1× 29 0.5× 45 448
Shaojun Zheng China 10 108 0.6× 139 1.0× 81 1.3× 77 1.2× 8 0.1× 51 436

Countries citing papers authored by E. GACS‐BAITZ

Since Specialization
Citations

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

Fields of papers citing papers by E. GACS‐BAITZ

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E. GACS‐BAITZ. 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 E. GACS‐BAITZ. The network helps show where E. GACS‐BAITZ may publish in the future.

Co-authorship network of co-authors of E. GACS‐BAITZ

This figure shows the co-authorship network connecting the top 25 collaborators of E. GACS‐BAITZ. A scholar is included among the top collaborators of E. GACS‐BAITZ 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 E. GACS‐BAITZ. E. GACS‐BAITZ 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.
Zappia, Giovanni, E. GACS‐BAITZ, Giuliano Delle Monache, et al.. (2008). ChemInform Abstract: Oxazolidin‐2‐one Ring, a Popular Framework in Synthetic Organic Chemistry. Part 2. Applications and Modifications. ChemInform. 39(34). 1 indexed citations
2.
Zappia, Giovanni, E. GACS‐BAITZ, Giuliano Delle Monache, et al.. (2007). Oxazolidin-2-one Ring, a Popular Framework in Synthetic Organic Chemistry Part 2 [1]. Applications and Modifications. Current Organic Synthesis. 4(3). 238–307. 41 indexed citations
3.
Zappia, Giovanni, E. GACS‐BAITZ, Giuliano Delle Monache, et al.. (2007). Oxazolidin-2-one Ring, a Popular Framework in Synthetic Organic Chemistry: Part 1. The Construction of the Oxazolidin-2-one Ring. Current Organic Synthesis. 4(1). 81–135. 54 indexed citations
4.
Botta, Bruno, et al.. (2003). Three isoflavanones with cannabinoid-like moieties from Desmodium canum. Phytochemistry. 64(2). 599–602. 19 indexed citations
5.
Minuti, Lucio, et al.. (2001). Stereoselective synthesis of enantiopure condensed [2.2]paracyclophanes. Tetrahedron Asymmetry. 12(8). 1179–1183. 16 indexed citations
6.
Catalano, Donata, Mario Cifelli, Katalin Fodor‐Csorba, et al.. (2000). Microscopic Organization and Tilt Angle in Smectic A and Chiral Smectic C Phases: Characterization and Orientational Order by 2H NMR and Electric Polarization Measurements. Molecular crystals and liquid crystals science technology. Section A, Molecular crystals and liquid crystals. 351(1). 245–257. 10 indexed citations
7.
Chiellini, Emo, Katalin Fodor‐Csorba, Giancarlo Galli, et al.. (1999). Partially Deuterated Side-Chain Liquid Crystalline Monomers and Polymers: Characterization and Order by 2H NMR. Molecular crystals and liquid crystals science technology. Section A, Molecular crystals and liquid crystals. 336(1). 111–122. 2 indexed citations
8.
Tommasi, Nunziatina De, Sonia Piacente, E. GACS‐BAITZ, et al.. (1998). Triterpenoid Saponins from Spergularia ramosa. Journal of Natural Products. 61(3). 323–327. 34 indexed citations
9.
Kardos, Julianna, et al.. (1996). Synthesis, anti-GABA activity and preferred conformation of bicuculline and norbicuculline enantiomers. European Journal of Medicinal Chemistry. 31(10). 761–765. 9 indexed citations
10.
Kuszmann, János & E. GACS‐BAITZ. (1996). O-Benzylidene Derivatives of D-Arabinose Diethyl and Dipropyl Dithioacetal. Australian Journal of Chemistry. 49(3). 273–280. 1 indexed citations
11.
GACS‐BAITZ, E., Lucio Minuti, & A. Taticchi. (1996). ChemInform Abstract: Synthesis and Complete 1H and 13C NMR Analysis of Some 4‐Androsten‐3‐ one Derivatives.. ChemInform. 27(46). 9 indexed citations
12.
Novak, Predrag, Dražen Vikić‐Topić, Zlatko Meić, & E. GACS‐BAITZ. (1996). Influence of a Side-Chain on Deuterium Isotope Effects in13C NMR Spectra of Some Benzene Derivatives. Magnetic Resonance in Chemistry. 34(8). 610–615. 4 indexed citations
13.
GACS‐BAITZ, E., et al.. (1995). Primary and secondary deuterium‐induced isotope effects for 13C NMR parameters of benzaldehyde. Magnetic Resonance in Chemistry. 33(6). 426–430. 4 indexed citations
14.
Fodor‐Csorba, Katalin, et al.. (1995). Synthesis of Liquid Crystals Containing Chlorine on the Chiral Center. Molecular crystals and liquid crystals science technology. Section A, Molecular crystals and liquid crystals. 265(1). 97–109. 5 indexed citations
15.
Takacs, Christopher J., et al.. (1994). pH control of the condensation reaction and its effect on the properties of formaldehyde/urea resins. Die Angewandte Makromolekulare Chemie. 215(1). 79–91. 6 indexed citations
16.
Fodor‐Csorba, Katalin, et al.. (1993). Deuterium labelled liquid crystalline compounds. Liquid Crystals. 14(6). 1863–1872. 5 indexed citations
17.
Ács, Mária, et al.. (1992). Comparison of the structures of the enantiomeric and racemic forms of an imidazo[2,1-b]thiazole anthelmintic agent and their hydrochlorides. Acta Crystallographica Section B Structural Science. 48(1). 88–95. 6 indexed citations
18.
Botta, Bruno, G. Delle Monache, E. GACS‐BAITZ, et al.. (1992). ChemInform Abstract: The Tetramerization of 2,4‐Dimethoxycinnamates. A Novel Route to Calixarenes.. ChemInform. 23(45). 1 indexed citations
19.
GACS‐BAITZ, E., et al.. (1991). cis-trans-Isomerization of [E]-5-(2-bromovinyl)-2,2′-anhydrouridinein vivoin rats. Xenobiotica. 21(3). 359–369. 1 indexed citations
20.
Aquino, Rita Patrizia, Francesco De Simone, F. F. Vincieri, Cosimo Pìzza, & E. GACS‐BAITZ. (1990). New Polyhydroxylated Triterpenes from Uncaria tomentosa. Journal of Natural Products. 53(3). 559–564. 88 indexed citations

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