Georg Manolikakes

4.6k total citations
95 papers, 3.8k citations indexed

About

Georg Manolikakes is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Georg Manolikakes has authored 95 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Organic Chemistry, 27 papers in Molecular Biology and 12 papers in Inorganic Chemistry. Recurrent topics in Georg Manolikakes's work include Catalytic C–H Functionalization Methods (35 papers), Sulfur-Based Synthesis Techniques (33 papers) and Chemical Synthesis and Reactions (21 papers). Georg Manolikakes is often cited by papers focused on Catalytic C–H Functionalization Methods (35 papers), Sulfur-Based Synthesis Techniques (33 papers) and Chemical Synthesis and Reactions (21 papers). Georg Manolikakes collaborates with scholars based in Germany, Egypt and China. Georg Manolikakes's co-authors include Shuai Liang, Paul Knochel, Nai‐Wei Liu, Kamil Hofman, Nai‐Wei Liu, Sebastian Bernhardt, Albrecht Metzger, Michael Bolte, Andrei Gavryushin and Matthias A. Schade and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and SHILAP Revista de lepidopterología.

In The Last Decade

Georg Manolikakes

93 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Georg Manolikakes Germany 36 3.5k 422 341 162 103 95 3.8k
Ponneri C. Ravikumar India 20 2.1k 0.6× 463 1.1× 464 1.4× 134 0.8× 108 1.0× 74 2.5k
Mario Waser Austria 29 2.4k 0.7× 509 1.2× 444 1.3× 240 1.5× 129 1.3× 127 2.8k
Lal Dhar S. Yadav India 36 4.3k 1.2× 583 1.4× 281 0.8× 132 0.8× 166 1.6× 231 4.5k
Yongwen Jiang China 26 3.4k 1.0× 471 1.1× 459 1.3× 127 0.8× 241 2.3× 63 3.7k
Krishna Nand Singh India 31 3.3k 0.9× 545 1.3× 292 0.9× 110 0.7× 118 1.1× 172 3.5k
Kou Hiroya Japan 32 3.5k 1.0× 508 1.2× 495 1.5× 197 1.2× 78 0.8× 90 3.9k
Pankaj Chauhan India 27 3.7k 1.0× 397 0.9× 511 1.5× 217 1.3× 93 0.9× 70 3.8k
Eddie L. Myers United Kingdom 26 2.6k 0.7× 357 0.8× 382 1.1× 195 1.2× 95 0.9× 39 2.8k
Torben Rogge Germany 30 2.7k 0.8× 211 0.5× 676 2.0× 248 1.5× 80 0.8× 47 2.9k
Nikolaos Kaplaneris Germany 29 2.8k 0.8× 587 1.4× 522 1.5× 313 1.9× 96 0.9× 38 3.0k

Countries citing papers authored by Georg Manolikakes

Since Specialization
Citations

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

Fields of papers citing papers by Georg Manolikakes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Georg Manolikakes

This figure shows the co-authorship network connecting the top 25 collaborators of Georg Manolikakes. A scholar is included among the top collaborators of Georg Manolikakes 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 Georg Manolikakes. Georg Manolikakes 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.
Kelm, Harald, et al.. (2025). Electrochemical Three‐component Synthesis of Alkenesulfonates from Cinnamic Acids, SO 2 , and Alcohols. ChemSusChem. 18(12). e202500186–e202500186. 2 indexed citations
2.
Schulig, Lukas, Georg Manolikakes, Dennis Schade, et al.. (2024). Targeting PARP-1 and DNA Damage Response Defects in Colorectal Cancer Chemotherapy with Established and Novel PARP Inhibitors. Cancers. 16(20). 3441–3441. 2 indexed citations
3.
Roos, Jessica, Georg Manolikakes, Uwe Schlomann, et al.. (2024). Nitro-fatty acids: promising agents for the development of new cancer therapeutics. Trends in Pharmacological Sciences. 45(11). 1061–1080. 2 indexed citations
4.
Niedner‐Schatteburg, Gereon, et al.. (2023). Glutathione kinetically outcompetes reactions between dimedone and a cyclic sulfenamide or physiological sulfenic acids. Free Radical Biology and Medicine. 208. 165–177. 4 indexed citations
6.
Schneider, Nico, et al.. (2023). Palladium-catalyzed enantioselective three-component synthesis of α-arylglycine derivatives from glyoxylic acid, sulfonamides and aryltrifluoroborates. Beilstein Journal of Organic Chemistry. 19. 719–726. 2 indexed citations
8.
Hofman, Kamil, et al.. (2021). Direct C–H-sulfonylation of 6-membered nitrogen-heteroaromatics. SHILAP Revista de lepidopterología. 1. 100003–100003. 18 indexed citations
9.
Manolikakes, Georg, et al.. (2021). Synthesis of Nitroolefins via the Direct Nitration of Alkenes. SynOpen. 5(3). 229–231. 6 indexed citations
11.
Bolte, Michael, et al.. (2021). Oxyenamides as Versatile Building Blocks for a Highly Stereoselective One‐Pot Synthesis of the 1,3‐Diamino‐2‐ol‐Scaffold Containing Three Continuous Stereocenters. Angewandte Chemie International Edition. 60(44). 23667–23671. 5 indexed citations
13.
Kelm, Harald, et al.. (2019). Manganese(iii) acetate-mediated direct C(sp2)–H-sulfonylation of enamides with sodium and lithium sulfinates. Organic & Biomolecular Chemistry. 17(22). 5538–5544. 26 indexed citations
14.
Bolte, Michael, et al.. (2019). An Enamide‐Based Domino Reaction for a Highly Stereoselective Synthesis of Tetrahydropyrans. Angewandte Chemie International Edition. 58(37). 13056–13059. 14 indexed citations
15.
Bolte, Michael, et al.. (2019). An Enamide‐Based Domino Reaction for a Highly Stereoselective Synthesis of Tetrahydropyrans. Angewandte Chemie. 131(37). 13190–13193. 4 indexed citations
16.
Kühn, Benjamin, Katharina J. Hock, Georg Manolikakes, et al.. (2018). Anti-inflammatory nitro-fatty acids suppress tumor growth by triggering mitochondrial dysfunction and activation of the intrinsic apoptotic pathway in colorectal cancer cells. Biochemical Pharmacology. 155. 48–60. 21 indexed citations
17.
Soltani, Yashar, et al.. (2016). 3-Component synthesis of α-substituted sulfonamides via Brønsted acid-catalyzed C(sp3)–H bond functionalization of 2-alkylazaarenes. Organic & Biomolecular Chemistry. 14(24). 5525–5528. 12 indexed citations
18.
Liang, Shuai & Georg Manolikakes. (2016). Copper‐Catalyzed Remote C−H Functionalization of 8‐Aminoquinolines with Sodium and Lithium Sulfinates. Advanced Synthesis & Catalysis. 358(15). 2371–2378. 65 indexed citations
19.
Dong, Zhi‐Bing, Georg Manolikakes, Lei Shi, Paul Knochel, & Herbert Mayr. (2009). Structure–Reactivity Relationships in Negishi Cross‐Coupling Reactions. Chemistry - A European Journal. 16(1). 248–253. 30 indexed citations
20.
Manolikakes, Georg, Navid Dastbaravardeh, & Paul Knochel. (2007). Nickel‐Catalyzed Cross‐Coupling Reactions of Aryltitanium(IV) Alkoxides with Aryl Halides.. ChemInform. 38(52). 1 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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