Clemens Stueckler

1.2k total citations
16 papers, 939 citations indexed

About

Clemens Stueckler is a scholar working on Molecular Biology, Inorganic Chemistry and Pharmacology. According to data from OpenAlex, Clemens Stueckler has authored 16 papers receiving a total of 939 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 5 papers in Inorganic Chemistry and 3 papers in Pharmacology. Recurrent topics in Clemens Stueckler's work include Enzyme Catalysis and Immobilization (15 papers), Microbial Metabolic Engineering and Bioproduction (6 papers) and Steroid Chemistry and Biochemistry (5 papers). Clemens Stueckler is often cited by papers focused on Enzyme Catalysis and Immobilization (15 papers), Microbial Metabolic Engineering and Bioproduction (6 papers) and Steroid Chemistry and Biochemistry (5 papers). Clemens Stueckler collaborates with scholars based in Austria and Germany. Clemens Stueckler's co-authors include Kurt Faber, Mélanie Hall, Wolfgang Kroutil, Peter Macheroux, Bernhard Hauer, Rainer Stuermer, Christoph K. Winkler, Karl Gruber, Nina Baudendistel and Gustav Oberdorfer and has published in prestigious journals such as Angewandte Chemie International Edition, Tetrahedron and Organic Letters.

In The Last Decade

Clemens Stueckler

16 papers receiving 924 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Clemens Stueckler Austria 13 840 250 178 108 106 16 939
Rainer Stuermer Austria 9 645 0.8× 197 0.8× 136 0.8× 79 0.7× 97 0.9× 12 777
Dorina Clay Austria 15 1.0k 1.2× 521 2.1× 202 1.1× 138 1.3× 115 1.1× 18 1.1k
Fei‐Fei Chen China 17 701 0.8× 231 0.9× 182 1.0× 60 0.6× 152 1.4× 39 858
Hannes Leisch Canada 15 485 0.6× 361 1.4× 88 0.5× 53 0.5× 145 1.4× 25 826
Sabry H. H. Younes Egypt 14 553 0.7× 366 1.5× 251 1.4× 130 1.2× 167 1.6× 40 1.0k
Jonathan Latham United Kingdom 8 415 0.5× 383 1.5× 195 1.1× 57 0.5× 74 0.7× 10 807
Verena Resch Austria 21 798 0.9× 424 1.7× 187 1.1× 66 0.6× 176 1.7× 26 1.1k
Klaus Edegger Austria 13 739 0.9× 201 0.8× 141 0.8× 60 0.6× 224 2.1× 15 894
Nan‐Wei Wan China 22 529 0.6× 672 2.7× 147 0.8× 69 0.6× 83 0.8× 69 1.2k
Véronique Alphand France 29 1.5k 1.8× 391 1.6× 155 0.9× 85 0.8× 446 4.2× 52 1.8k

Countries citing papers authored by Clemens Stueckler

Since Specialization
Citations

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

Fields of papers citing papers by Clemens Stueckler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Clemens Stueckler

This figure shows the co-authorship network connecting the top 25 collaborators of Clemens Stueckler. A scholar is included among the top collaborators of Clemens Stueckler 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 Clemens Stueckler. Clemens Stueckler is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Oberdorfer, Gustav, Georg Steinkellner, Clemens Stueckler, Kurt Faber, & Karl Gruber. (2011). Stereopreferences of Old Yellow Enzymes: Structure Correlations and Sequence Patterns in Enoate Reductases. ChemCatChem. 3(10). 1562–1566. 33 indexed citations
2.
Stueckler, Clemens, Christoph K. Winkler, Mélanie Hall, et al.. (2011). Stereo‐Controlled Asymmetric Bioreduction of α,β‐Dehydroamino Acid Derivatives. Advanced Synthesis & Catalysis. 353(7). 1169–1173. 37 indexed citations
3.
Stueckler, Clemens, Christoph K. Winkler, Silvia M. Glueck, et al.. (2010). Bioreduction of α-methylcinnamaldehyde derivatives: chemo-enzymatic asymmetric synthesis of Lilial™ and Helional™. Dalton Transactions. 39(36). 8472–8472. 50 indexed citations
4.
5.
Winkler, Christoph K., et al.. (2010). Asymmetric Synthesis of O‐Protected Acyloins Using Enoate Reductases: Stereochemical Control through Protecting Group Modification. European Journal of Organic Chemistry. 2010(33). 6354–6358. 25 indexed citations
6.
Stueckler, Clemens, Christoph K. Winkler, Melanie Bonnekessel, & Kurt Faber. (2010). Asymmetric Synthesis of (R)‐3‐Hydroxy‐2‐methylpropanoate (‘Roche Ester’) and Derivatives via Biocatalytic CC‐Bond Reduction. Advanced Synthesis & Catalysis. 352(14-15). 2663–2666. 45 indexed citations
7.
Stueckler, Clemens, et al.. (2009). Epoxidation of conjugated CC-bonds and sulfur-oxidation of thioethers mediated by NADH:FMN-dependent oxidoreductases. Organic & Biomolecular Chemistry. 7(6). 1115–1115. 22 indexed citations
8.
Stueckler, Clemens, Tamara Reiter, Nina Baudendistel, & Kurt Faber. (2009). Nicotinamide-independent asymmetric bioreduction of CC-bonds via disproportionation of enones catalyzed by enoate reductases. Tetrahedron. 66(3). 663–667. 62 indexed citations
9.
Hall, Mélanie, Clemens Stueckler, Bernhard Hauer, et al.. (2008). Asymmetric Bioreduction of Activated C=C Bonds Using Zymomonas mobilis NCR Enoate Reductase and Old Yellow Enzymes OYE 1–3 from Yeasts. European Journal of Organic Chemistry. 2008(9). 1511–1516. 148 indexed citations
10.
Hall, Mélanie, Clemens Stueckler, Bernhard Hauer, et al.. (2008). Asymmetric Bioreduction of Activated C=C Bonds Using Zymomonas mobilis NCR Enoate Reductase and Old Yellow Enzymes OYE 1–3 from Yeasts (Eur. J. Org. Chem. 9/2008). European Journal of Organic Chemistry. 2008(9). 1479–1479. 1 indexed citations
11.
Hall, Mélanie, Clemens Stueckler, Gustav Oberdorfer, et al.. (2008). Asymmetric Bioreduction of CC Bonds using Enoate Reductases OPR1, OPR3 and YqjM: Enzyme‐Based Stereocontrol. Advanced Synthesis & Catalysis. 350(3). 411–418. 155 indexed citations
12.
Hall, Mélanie, Clemens Stueckler, Wolfgang Kroutil, Peter Macheroux, & Kurt Faber. (2007). Asymmetric Bioreduction of Activated Alkenes Using Cloned 12‐Oxophytodienoate Reductase Isoenzymes OPR‐1 and OPR‐3 from Lycopersicon esculentum (Tomato): A Striking Change of Stereoselectivity. Angewandte Chemie International Edition. 46(21). 3934–3937. 141 indexed citations
13.
14.
Hall, Mélanie, Clemens Stueckler, Wolfgang Kroutil, Peter Macheroux, & Kurt Faber. (2007). Asymmetric Bioreduction of Activated Alkenes Using Cloned 12‐Oxophytodienoate Reductase Isoenzymes OPR‐1 and OPR‐3 from Lycopersicon esculentum (Tomato): A Striking Change of Stereoselectivity. Angewandte Chemie. 119(21). 4008–4011. 57 indexed citations
15.
Hall, Mélanie, Clemens Stueckler, Wolfgang Kroutil, Peter Macheroux, & Kurt Faber. (2007). Enantioselective Reduction of Activated Olefins Using ‘Old Yellow Enzymes’. Synfacts. 2007(7). 757–757. 2 indexed citations
16.
Hall, Mélanie, Clemens Stueckler, Wolfgang Kroutil, Peter Macheroux, & Kurt Faber. (2007). Asymmetric Bioreduction of Activated Alkenes Using Cloned 12‐Oxophytodienoate Reductase Isoenzymes OPR‐1 and OPR‐3 from Lycopersicon esculentum (Tomato): A Striking Change of Stereoselectivity.. ChemInform. 38(36). 2 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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