Mario Waser

3.5k total citations
127 papers, 2.8k citations indexed

About

Mario Waser is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Mario Waser has authored 127 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 118 papers in Organic Chemistry, 26 papers in Molecular Biology and 20 papers in Inorganic Chemistry. Recurrent topics in Mario Waser's work include Asymmetric Synthesis and Catalysis (51 papers), Synthetic Organic Chemistry Methods (27 papers) and Oxidative Organic Chemistry Reactions (23 papers). Mario Waser is often cited by papers focused on Asymmetric Synthesis and Catalysis (51 papers), Synthetic Organic Chemistry Methods (27 papers) and Oxidative Organic Chemistry Reactions (23 papers). Mario Waser collaborates with scholars based in Austria, Germany and Italy. Mario Waser's co-authors include Johanna Novacek, Johannes Schörgenhumer, Cristina Nevado, Alois Fürstner, Olga Garcı́a Mancheño, Raphaël Robiette, Martin Tremblay, António Massa, Heinz Falk and Markus Himmelsbach 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

Mario Waser

126 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mario Waser Austria 29 2.4k 509 444 240 156 127 2.8k
Corinna S. Schindler United States 32 2.7k 1.1× 633 1.2× 456 1.0× 133 0.6× 187 1.2× 84 3.0k
Steven W. M. Crossley United States 11 1.8k 0.7× 443 0.9× 528 1.2× 158 0.7× 126 0.8× 12 2.4k
Oleg V. Larionov United States 39 3.5k 1.4× 746 1.5× 401 0.9× 322 1.3× 161 1.0× 102 4.0k
Jonathan T. Reeves United States 33 3.1k 1.3× 788 1.5× 872 2.0× 283 1.2× 123 0.8× 84 3.5k
Chun‐An Fan China 37 4.4k 1.8× 564 1.1× 739 1.7× 195 0.8× 254 1.6× 104 4.7k
Yannick Landais France 36 4.3k 1.8× 637 1.3× 592 1.3× 379 1.6× 95 0.6× 168 4.8k
Arkady Krasovskiy Germany 34 4.8k 1.9× 561 1.1× 707 1.6× 284 1.2× 92 0.6× 56 5.2k
Yoo Tanabe Japan 32 2.5k 1.0× 740 1.5× 282 0.6× 133 0.6× 140 0.9× 140 2.9k
David M. Hodgson United Kingdom 35 4.0k 1.6× 597 1.2× 544 1.2× 138 0.6× 162 1.0× 184 4.3k
Sentaro Okamoto Japan 32 3.1k 1.3× 458 0.9× 516 1.2× 166 0.7× 93 0.6× 145 3.3k

Countries citing papers authored by Mario Waser

Since Specialization
Citations

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

Fields of papers citing papers by Mario Waser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mario Waser

This figure shows the co-authorship network connecting the top 25 collaborators of Mario Waser. A scholar is included among the top collaborators of Mario Waser 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 Mario Waser. Mario Waser 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.
2.
Bechmann, Matthias, et al.. (2025). Determination of the pKaH of Established Isothiourea Catalysts. European Journal of Organic Chemistry. 28(13). 3 indexed citations
3.
Ofial, Armin R., et al.. (2025). From Oxygen to Tellurium: The Impact of the Chalcogen on Nucleophilicities and Basicities of Isochalcogenourea Catalysts. Angewandte Chemie International Edition. 64(48). e202514865–e202514865. 1 indexed citations
4.
Mayer, Péter, et al.. (2024). Enantioselective Syntheses of 3,4‐Dihydropyrans Employing Isochalcogenourea‐Catalyzed Formal (4+2)‐Cycloadditions of Allenoates. Advanced Synthesis & Catalysis. 366(9). 2115–2122. 9 indexed citations
5.
Monkowius, Uwe, et al.. (2023). Cooperative Chiral Lewis Base/Palladium‐Catalyzed Asymmetric Syntheses of Methylene‐Containing δ‐Lactams. European Journal of Organic Chemistry. 26(45). e202300982–e202300982. 4 indexed citations
6.
Mayer, Péter, et al.. (2023). Chiral Isochalcogenourea‐Catalysed Enantioselective (4+2) Cycloadditions of Allenoates. Angewandte Chemie International Edition. 63(2). e202315345–e202315345. 17 indexed citations
7.
Požgan, Franc, et al.. (2023). Synthesis and Catalytic Activity of Bifunctional Phase-Transfer Organocatalysts Based on Camphor. Molecules. 28(3). 1515–1515. 3 indexed citations
8.
Himmelsbach, Markus, et al.. (2023). Dibenzoylperoxide‐Mediated Oxidative α‐Thio/Seleno‐Cyanation of β‐Ketoesters and Oxindoles. European Journal of Organic Chemistry. 26(46). 3 indexed citations
9.
Bechmann, Matthias, et al.. (2023). Chiral Lewis Base‐Catalysed Asymmetric Syntheses of Benzo‐fused ϵ‐Lactones. European Journal of Organic Chemistry. 26(39). e202300704–e202300704. 5 indexed citations
10.
Schörgenhumer, Johannes, et al.. (2022). Stereoselective Syntheses of Masked β‐Amino Acid Containing Phthalides. Helvetica Chimica Acta. 105(11). e202200110–e202200110. 3 indexed citations
11.
Mallojjala, Sharath Chandra, et al.. (2021). Enantioselective Catalytic Synthesis of α-Halogenated α-Aryl-β2,2-amino Acid Derivatives. SHILAP Revista de lepidopterología. 2(1). 34–43. 14 indexed citations
12.
Waser, Mario, et al.. (2021). Chiral isothiourea-catalyzed kinetic resolution of 4-hydroxy[2.2]paracyclophane. Beilstein Journal of Organic Chemistry. 17. 800–804. 7 indexed citations
13.
14.
Winter, Michael, et al.. (2019). Quaternary β2,2-amino acid derivatives by asymmetric addition of isoxazolidin-5-ones to para-quinone methides. Chemical Communications. 56(4). 579–582. 41 indexed citations
15.
Yang, Fan, et al.. (2018). Synthesis of Cyclic Organic Carbonates Using Atmospheric Pressure CO2 and Charge-Containing Thiourea Catalysts. The Journal of Organic Chemistry. 83(17). 9991–10000. 45 indexed citations
16.
Widhalm, Michael, et al.. (2018). Syntheses of Highly Functionalized Spirocyclohexenes by Formal [4+2] Annulation of Arylidene Azlactones with Allenoates. Asian Journal of Organic Chemistry. 7(8). 1620–1625. 7 indexed citations
17.
Schörgenhumer, Johannes & Mario Waser. (2018). Transition metal-free coupling of terminal alkynes and hypervalent iodine-based alkyne-transfer reagents to access unsymmetrical 1,3-diynes. Organic & Biomolecular Chemistry. 16(41). 7561–7563. 10 indexed citations
18.
Schörgenhumer, Johannes & Mario Waser. (2016). New strategies and applications using electrophilic cyanide-transfer reagents under transition metal-free conditions. Organic Chemistry Frontiers. 3(11). 1535–1540. 60 indexed citations
19.
Robiette, Raphaël, et al.. (2016). Benzylic Ammonium Ylide Mediated Epoxidations. Synlett. 27(13). 1963–1968. 15 indexed citations
20.
Waser, Mario, et al.. (2012). Investigations Concerning the Syntheses of TADDOL-Derived Secondary Amines and Their Use To Access Novel Chiral Organocatalysts. Synthesis. 44(23). 3661–3670. 25 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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