Marko Hapke

3.3k total citations · 1 hit paper
66 papers, 2.8k citations indexed

About

Marko Hapke is a scholar working on Organic Chemistry, Inorganic Chemistry and Oncology. According to data from OpenAlex, Marko Hapke has authored 66 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Organic Chemistry, 20 papers in Inorganic Chemistry and 7 papers in Oncology. Recurrent topics in Marko Hapke's work include Catalytic Alkyne Reactions (27 papers), Catalytic C–H Functionalization Methods (21 papers) and Asymmetric Hydrogenation and Catalysis (15 papers). Marko Hapke is often cited by papers focused on Catalytic Alkyne Reactions (27 papers), Catalytic C–H Functionalization Methods (21 papers) and Asymmetric Hydrogenation and Catalysis (15 papers). Marko Hapke collaborates with scholars based in Germany, Austria and United States. Marko Hapke's co-authors include Bárbara Heller, N. Weding, John F. Hartwig, Arne Lützen, Tatsuo Ishiyama, Jaclyn M. Murphy, Norio Miyaura, Anke Spannenberg, Indre Thiel and Charles Edwin Webster and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Society Reviews and Angewandte Chemie International Edition.

In The Last Decade

Marko Hapke

64 papers receiving 2.7k citations

Hit Papers

The fascinating construction of pyridine ring systems by ... 2007 2026 2013 2019 2007 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marko Hapke Germany 25 2.5k 658 203 182 178 66 2.8k
Huaiqing Zhao China 25 2.2k 0.9× 502 0.8× 386 1.9× 166 0.9× 333 1.9× 77 2.9k
Shuichi Ôi Japan 33 2.9k 1.1× 988 1.5× 173 0.9× 178 1.0× 380 2.1× 77 3.4k
Fabiano Visentin Italy 29 2.1k 0.8× 560 0.9× 179 0.9× 55 0.3× 173 1.0× 130 2.5k
Wanxiang Zhao China 25 2.1k 0.8× 419 0.6× 265 1.3× 82 0.5× 196 1.1× 83 2.4k
Hiroshi Danjo Japan 18 1.3k 0.5× 586 0.9× 295 1.5× 81 0.4× 230 1.3× 44 1.5k
Diana A. Iovan United States 21 902 0.4× 571 0.9× 173 0.9× 86 0.5× 255 1.4× 25 1.4k
Kei Murakami Japan 32 3.4k 1.4× 389 0.6× 199 1.0× 88 0.5× 355 2.0× 96 3.7k
Xing‐Wang Wang China 30 2.4k 1.0× 849 1.3× 348 1.7× 75 0.4× 336 1.9× 83 3.0k
Fumitoshi Shibahara Japan 28 2.2k 0.9× 706 1.1× 212 1.0× 58 0.3× 173 1.0× 55 2.4k
Matthias Otte Germany 18 962 0.4× 403 0.6× 123 0.6× 127 0.7× 288 1.6× 32 1.2k

Countries citing papers authored by Marko Hapke

Since Specialization
Citations

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

Fields of papers citing papers by Marko Hapke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marko Hapke

This figure shows the co-authorship network connecting the top 25 collaborators of Marko Hapke. A scholar is included among the top collaborators of Marko Hapke 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 Marko Hapke. Marko Hapke 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.
Denifl, Peter, et al.. (2023). Recent Advances in Catalytic Chemical Recycling of Polyolefins. ChemCatChem. 15(13). 62 indexed citations
2.
Cı́sařová, Ivana, et al.. (2023). Cyclotrimerization Approach to Symmetric [9]Helical Indenofluorenes: Diverting Cyclization Pathways. Chemistry - A European Journal. 29(58). e202301491–e202301491. 5 indexed citations
3.
Jiao, Haijun, et al.. (2021). Synthesis of Phosphinines from CoII-Catalyzed [2+2+2] Cycloaddition Reactions. ACS Catalysis. 11(21). 13434–13444. 15 indexed citations
4.
Fischer, Fabian, et al.. (2020). CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity. Catalysis Science & Technology. 10(23). 8005–8014. 5 indexed citations
5.
Fischer, Fabian & Marko Hapke. (2018). Air‐Stable CpCoI–Phosphite–Fumarate Precatalyst in Cyclization Reactions: Comparing Different Methods of Energy Supply. European Journal of Organic Chemistry. 2018(24). 3193–3201. 8 indexed citations
6.
Thiel, Indre, et al.. (2017). Insight into the Activation of In Situ Generated Chiral RhI Catalysts and Their Application in Cyclotrimerizations. Chemistry - A European Journal. 23(67). 17048–17057. 10 indexed citations
7.
Fischer, Fabian, et al.. (2016). In Situ-Generated Chiral Co(I)-Catalyst for Asymmetric [2+2+2] Cycloadditions of Triynes. ACS Catalysis. 6(5). 3025–3029. 27 indexed citations
8.
Fischer, Fabian, et al.. (2015). CoCl(PPh3)3 as Cyclotrimerization Catalyst for Functionalized Triynes under Mild Conditions. The Journal of Organic Chemistry. 80(19). 9781–9793. 24 indexed citations
9.
Hapke, Marko & Carl Christoph Tzschucke. (2013). Asymmetrische Katalyse mit chiralen Cyclopentadienylrhodiumkomplexen. Angewandte Chemie. 125(12). 3399–3401. 3 indexed citations
10.
Hapke, Marko & Carl Christoph Tzschucke. (2013). Achieving Enantioselectivity with Chiral Cyclopentadienylrhodium Complexes. Angewandte Chemie International Edition. 52(12). 3317–3319. 9 indexed citations
11.
Thiel, Indre & Marko Hapke. (2013). Computational Studies and Experimental Results—An Example of Excellent Teamwork in Studying Carbocyclization. Angewandte Chemie International Edition. 52(23). 5916–5918. 8 indexed citations
12.
Weding, N., Anke Spannenberg, Ralf Jackstell, & Marko Hapke. (2012). Formation and Reactivity of a Co4-μ-Alkyne Cluster from a Co(I)-Alkene Complex. Organometallics. 31(15). 5660–5663. 9 indexed citations
13.
Hapke, Marko, et al.. (2012). Investigations on the synthesis of monoarylated diynes by monoprotection/cross-coupling/deprotection approach. Tetrahedron Letters. 53(23). 2856–2859. 3 indexed citations
14.
Hapke, Marko, et al.. (2011). Metal‐Free Cyclotrimerization for the De Novo Synthesis of Pyridines. Angewandte Chemie International Edition. 50(11). 2434–2435. 40 indexed citations
15.
Hapke, Marko, N. Weding, & Anke Spannenberg. (2010). Bis(dimethyl sulfoxide)hydridobis(triphenylphosphane)cobalt(I). Acta Crystallographica Section E Structure Reports Online. 66(8). m1031–m1031. 3 indexed citations
16.
Hapke, Marko, N. Weding, & Anke Spannenberg. (2010). Highly Reactive Cyclopentadienylcobalt(I) Olefin Complexes. Organometallics. 29(19). 4298–4304. 50 indexed citations
17.
Hapke, Marko, A. Wöhl, Stephan Peitz, et al.. (2009). [N,N-Bis(diphenylphosphino)isopropylamine]dibromidonickel(II). Acta Crystallographica Section E Structure Reports Online. 65(3). m252–m252. 4 indexed citations
18.
Albrecht, Markus, Ingo Janser, Arne Lützen, et al.. (2005). 5,5′‐Diamino‐2,2′‐bipyridine: A Versatile Building Block for the Synthesis of Bipyridine/Catechol Ligands That Form Homo‐ and Heteronuclear Helicates. Chemistry - A European Journal. 11(19). 5742–5748. 30 indexed citations
19.
Lützen, Arne, et al.. (2003). Synthesis of Differently Disubstituted 2,2′‐Bipyridines by a Modified Negishi Cross‐Coupling Reaction. European Journal of Organic Chemistry. 2003(20). 3948–3957. 28 indexed citations
20.
Lützen, Arne, Marko Hapke, & Sven Meyer. (2002). Synthesis of Bis(BINOL) Substituted 2,2′-Bipyridines and their Late Transition Metal Complexes. Synthesis. 2289–2295. 9 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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