Matthias Heydenreich

3.3k total citations
152 papers, 2.6k citations indexed

About

Matthias Heydenreich is a scholar working on Molecular Biology, Organic Chemistry and Plant Science. According to data from OpenAlex, Matthias Heydenreich has authored 152 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 54 papers in Organic Chemistry and 47 papers in Plant Science. Recurrent topics in Matthias Heydenreich's work include Bioactive natural compounds (34 papers), Natural product bioactivities and synthesis (23 papers) and Bioactive Compounds and Antitumor Agents (21 papers). Matthias Heydenreich is often cited by papers focused on Bioactive natural compounds (34 papers), Natural product bioactivities and synthesis (23 papers) and Bioactive Compounds and Antitumor Agents (21 papers). Matthias Heydenreich collaborates with scholars based in Germany, Kenya and Hungary. Matthias Heydenreich's co-authors include Abiy Yenesew, Jacob O. Midiwo, Martin G. Peter, Erich Kleinpeter, Solomon Derese, Andreas Koch, Hoseah M. Akala, Ferenc Fülöp, István Szatmári and Martin Steup and has published in prestigious journals such as SHILAP Revista de lepidopterología, Cell Metabolism and Macromolecules.

In The Last Decade

Matthias Heydenreich

149 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthias Heydenreich Germany 28 1.1k 826 772 279 228 152 2.6k
Warinthorn Chavasiri Thailand 30 1.1k 1.0× 1.2k 1.4× 732 0.9× 316 1.1× 136 0.6× 193 3.3k
Nguyễn Mạnh Cường Vietnam 29 1.3k 1.2× 486 0.6× 724 0.9× 239 0.9× 361 1.6× 145 2.3k
Gabriel Navarrete‐Vázquez Mexico 35 1.2k 1.1× 1.5k 1.8× 348 0.5× 306 1.1× 101 0.4× 145 3.6k
Pascal Richomme France 32 811 0.7× 552 0.7× 665 0.9× 240 0.9× 114 0.5× 132 2.9k
Dulce Helena Siqueira Silva Brazil 33 1.1k 1.0× 494 0.6× 1.0k 1.4× 408 1.5× 149 0.7× 139 2.9k
Somdej Kanokmedhakul Thailand 27 754 0.7× 489 0.6× 598 0.8× 716 2.6× 262 1.1× 119 2.1k
L. Mark Cosentino United States 23 1.8k 1.6× 876 1.1× 563 0.7× 414 1.5× 283 1.2× 30 3.0k
Aurea Echevarrı́a Brazil 29 761 0.7× 1.3k 1.6× 582 0.8× 106 0.4× 92 0.4× 153 3.0k
Ángel G. Ravelo Spain 33 2.0k 1.8× 1.1k 1.4× 724 0.9× 396 1.4× 173 0.8× 153 3.9k
Koneni V. Sashidhara India 39 1.2k 1.1× 2.2k 2.7× 391 0.5× 737 2.6× 172 0.8× 141 3.9k

Countries citing papers authored by Matthias Heydenreich

Since Specialization
Citations

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

Fields of papers citing papers by Matthias Heydenreich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthias Heydenreich

This figure shows the co-authorship network connecting the top 25 collaborators of Matthias Heydenreich. A scholar is included among the top collaborators of Matthias Heydenreich 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 Matthias Heydenreich. Matthias Heydenreich 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.
Nondo, Ramadhani S.O., et al.. (2024). Therapeutic potential of Zanha africana (Radlk.) Exell: antimycobacterial activity and safety evaluation. Scientific African. 26. e02371–e02371. 1 indexed citations
2.
Poleschner, Helmut, Matthias Heydenreich, & Andreas J. Achazi. (2023). Epimerization of trans‐Cycloalkenes with the X−C=C−SeR*‐Unit – The Steric Demand of X=H, F, Cl, Br, I, Me, Et and CF3. European Journal of Organic Chemistry. 26(43).
3.
Namukobe, Jane, Patrick Vudriko, Godwin Anywar, et al.. (2023). In Vitro Anti-Venom Potentials of Aqueous Extract and Oils of Toona ciliata M. Roem against Cobra Venom and Chemical Constituents of Oils. Molecules. 28(7). 3089–3089. 1 indexed citations
5.
Namukobe, Jane, Matthias Heydenreich, Willy Ssengooba, et al.. (2023). Two new compounds and the anti-mycobacterial activity of the constituents from Zanthoxylum leprieurii root bark. Phytochemistry Letters. 54. 107–113. 4 indexed citations
6.
Innocent, Ester, Ramadhani S.O. Nondo, Francis Machumi, et al.. (2023). Bioassay-guided isolation of antimycobacterial compounds from Aphloia theiformis (Vahl) Benn root ethanolic extract. Phytomedicine Plus. 3(1). 100406–100406. 3 indexed citations
7.
Heydenreich, Matthias, et al.. (2022). Benzylic Fluorination Induced by a Charge-Transfer Complex with a Solvent-Dependent Selectivity Switch. Organic Letters. 24(29). 5376–5380. 17 indexed citations
8.
Becerra, José, Jaime R. Cabrera‐Pardo, Bernd Schmidt, et al.. (2022). Bromination of eudesmin isolated from araucaria araucana induces epimerization and give bromine derivatives with loss of anti-Candida activity. Natural Product Research. 37(14). 2466–2471. 1 indexed citations
9.
Innocent, Ester, Kerstin Andrae‐Marobela, Francis Machumi, et al.. (2022). Safety evaluation and bioassay-guided isolation of antimycobacterial compounds from Morella salicifolia root ethanolic extract. Journal of Ethnopharmacology. 296. 115501–115501. 8 indexed citations
10.
Ngassapa, Olipa, Mainen J. Moshi, Francis Machumi, et al.. (2020). In vitro antioxidant and cytotoxic activity of the root extract of Aspilia mossambicensis (Oliv) Wild (Asteraceae). Journal of Medicinal Plants Research. 14(11). 613–624. 1 indexed citations
11.
Yang, Li, Solomon Derese, Albert Ndakala, et al.. (2019). Cytotoxicity of isoflavones from Millettia dura. Natural Product Research. 35(16). 2744–2747. 12 indexed citations
12.
Hildebrand, Viet, Matthias Heydenreich, André Laschewsky, et al.. (2017). “Schizophrenic” self-assembly of dual thermoresponsive block copolymers bearing a zwitterionic and a non-ionic hydrophilic block. Polymer. 122. 347–357. 35 indexed citations
13.
Koch, Andreas, Eric M. Guantai, Solomon Derese, et al.. (2017). Alkenyl cyclohexanone derivatives from Lannea rivae and Lannea schweinfurthii. Phytochemistry Letters. 23. 141–148. 16 indexed citations
14.
Paz, Cristian, José Becerra, Mario Silva, et al.. (2016). (-)-8-Oxohobartine a New İndole Alkaloid from Aristotelia chilensis (Mol.) Stuntz. SHILAP Revista de lepidopterología. 8 indexed citations
15.
Innocent, Ester, et al.. (2015). Comparison of cycloartenone from four insecticidal Kotschya species (Fabaceae) harvested during dry and wet seasons. Journal of Pharmacognosy and Phytochemistry. 4(4). 97–102. 2 indexed citations
16.
Irungu, Beatrice, Jennifer Orwa, Francis Kimani, et al.. (2015). Antiplasmodial and cytotoxic activities of the constituents of Turraea robusta and Turraea nilotica. Journal of Ethnopharmacology. 174. 419–425. 24 indexed citations
17.
Yenesew, Abiy, Hannington Twinomuhwezi, Hoseah M. Akala, et al.. (2009). Antiplasmodial and larvicidal flavonoids from Derris trifoliate. SHILAP Revista de lepidopterología. 1 indexed citations
18.
Joseph, Cosam C., Mayunga H.H. Nkunya, Stephen Magesa, et al.. (2009). Larvicidal and IGR activity of extract of Tanzanian plants against malaria vector mosquitoes.. SHILAP Revista de lepidopterología. 46(2). 145–52. 41 indexed citations
19.
Erk, Çakıl, et al.. (2006). Investigation of the Cation Complexation by Macrocyclic Ethers using 13C NMR Spin--Lattice Dipolar Relaxation Time Measurements. DergiPark (Istanbul University). 1 indexed citations
20.
Poleschner, Helmut, Matthias Heydenreich, & Uwe Schilde. (2000). Reactions of RSe–EMe3 (E = Si, Ge, Sn, Pb) with XeF2 — RSe–F Equivalents in the Fluoroselenenylation of Acetylenes[1]. European Journal of Inorganic Chemistry. 2000(6). 1307–1313. 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026