Max Knollmüller

473 total citations
40 papers, 386 citations indexed

About

Max Knollmüller is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Max Knollmüller has authored 40 papers receiving a total of 386 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Organic Chemistry, 20 papers in Molecular Biology and 13 papers in Spectroscopy. Recurrent topics in Max Knollmüller's work include Chemical Synthesis and Analysis (13 papers), Asymmetric Synthesis and Catalysis (13 papers) and Analytical Chemistry and Chromatography (10 papers). Max Knollmüller is often cited by papers focused on Chemical Synthesis and Analysis (13 papers), Asymmetric Synthesis and Catalysis (13 papers) and Analytical Chemistry and Chromatography (10 papers). Max Knollmüller collaborates with scholars based in Austria and Germany. Max Knollmüller's co-authors include Christian R. Noe, Horst Völlenkle, Peter Gärtner, Ernst Wagner, Peter Ettmayer, Berndt Oberhauser, K. Mereiter, Matthew Cotten, Armin Holzner and G. Schaffner and has published in prestigious journals such as Nucleic Acids Research, Synthesis and European Journal of Organic Chemistry.

In The Last Decade

Max Knollmüller

38 papers receiving 377 citations

Peers

Max Knollmüller

SPECT

Mohindra S. Chadha India

James D. Carroll United States

Günter Losse Germany

Frank Moffatt United Kingdom

Patrizia Giorgianni Italy

Sarah Y. Fulford United Kingdom

Joan M. Caroon United States

Douglas S. Masterson United States

R. Charles Israel

József Schindler Hungary

Mohindra S. Chadha India

Max Knollmüller

269 ×1.1

104 ×0.5

34 ×0.3

SPECT

55 ×1.0

58 ×1.5

Citations per year, relative to Max Knollmüller Max Knollmüller (= 1×) peers Mohindra S. Chadha

Countries citing papers authored by Max Knollmüller

Since Specialization

Citations

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

Fields of papers citing papers by Max Knollmüller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Max Knollmüller

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Noe, Christian R., et al.. (2008). Increasing chiral recognition in acetal formation. Chirality. 21(4). 428–435. 4 indexed citations

Gärtner, Peter, et al.. (2002). A facile and high yielding synthesis of 2,2,3,4,4-d5-androsterone-β-d-glucuronide—an internal standard in dope analysis. Steroids. 68(1). 85–96. 8 indexed citations

Gärtner, Peter, et al.. (2001). Lithium tri-sec-butylborodeuteride: a new reagent for the stereoselective deuterium addition to cyclohexanones with single chair conformations. ARKIVOC. 2001(2). 9–20. 6 indexed citations

Gärtner, Peter, et al.. (2000). [1,2]-Wittig rearrangement of acetals. Part 2: The influence of reaction conditions. Tetrahedron Asymmetry. 11(4). 1003–1013. 5 indexed citations

Gärtner, Peter, et al.. (1999). [1,2]-Wittig rearrangement of acetals. Part 1: Investigation about structural requirements. Tetrahedron Asymmetry. 10(24). 4811–4830. 3 indexed citations

Knollmüller, Max, et al.. (1999). Enantioselective addition of organometallics to aldehydes using camphor derived chiral 1,4-aminoalcohols as ligands. Tetrahedron Asymmetry. 10(20). 3969–3975. 36 indexed citations

Knollmüller, Max, et al.. (1998). Addition von enantiomerenreinen Aminen an aktivierte Olefine, 1. Mitt. Über die Addition an ω;-Nitrostyrol. Monatshefte für Chemie - Chemical Monthly. 129(10). 1025–1033. 2 indexed citations

Knollmüller, Max, et al.. (1998). Acetals as Chiral Ligands for Organomagnesium and Organolithium Compounds. Monatshefte für Chemie - Chemical Monthly. 129(8-9). 953–959. 2 indexed citations

Knollmüller, Max, et al.. (1998). New camphor derived chiral ligands for asymmetric synthesis. Tetrahedron Asymmetry. 9(22). 4009–4020. 12 indexed citations

10.

Knollmüller, Max, et al.. (1998). Acetale als chirale Liganden für organische Magnesium- und Lithiumverbindungen. Monatshefte für Chemie - Chemical Monthly. 129(8). 953–953. 1 indexed citations

11.

Noe, Christian R., et al.. (1995). Chiral lactols, XIII. On the determination of the absolute configuration of aromatic cyanohydrins and structurally related compounds. Liebigs Annalen. 1995(7). 1353–1360. 5 indexed citations

12.

Noe, Christian R., et al.. (1994). Chirale Lactole, XII. Untersuchungen zur basenkatalysierten Glycolaldehydaldolisierung. Liebigs Annalen der Chemie. 1994(6). 611–613. 6 indexed citations

13.

Wagner, Ernst, Berndt Oberhauser, Armin Holzner, et al.. (1991). A simple procedure for the preparation of protected 2′-O-methyl or 2′-O-ethyl ribonucleoside-3′-O-phosphoramidites. Nucleic Acids Research. 19(21). 5965–5971. 35 indexed citations

14.

Noe, Christian R., Max Knollmüller, & Peter Ettmayer. (1991). Chirale Lactole, X. Allose als Hauptprodukt der Glycolaldehyd‐Trimerisierung. Liebigs Annalen der Chemie. 1991(5). 417–424. 13 indexed citations

15.

Noe, Christian R., Max Knollmüller, & Peter Ettmayer. (1989). Chirale Lactole, VIII Ein Weg zur asymmetrischen Induktion bei der Bildung von Zuckern. Liebigs Annalen der Chemie. 1989(7). 637–643. 9 indexed citations

16.

Noe, Christian R., et al.. (1989). Chirale Lactole, IX Vergleichende Untersuchungen zur Reaktivität von Lactolen und α‐Hydroxylactolen. Liebigs Annalen der Chemie. 1989(7). 645–650. 2 indexed citations

17.

Knollmüller, Max, et al.. (1986). Enantiomer-selektive Acetal-Bildung, ein Verfahren zur Reinherstellung bzw. Anreicherung von Enantiomeren. Synthesis. 1986(6). 501–505. 5 indexed citations

18.

Knollmüller, Max, et al.. (1975). Über Dialkylidensulfamide. Monatshefte für Chemie - Chemical Monthly. 106(5). 1095–1102. 8 indexed citations

19.

Hromatka, O., et al.. (1966). Piperazinsubstituierte Isochinolinderivate. Monatshefte für Chemie - Chemical Monthly. 97(1). 19–32. 1 indexed citations

20.

Hromatka, O., Max Knollmüller, & F. Sauter. (1962). Untersuchungen über Phenthiazinderivate, 18. Mitt. Neue Derivate desα-Oxo-4, 10-trimethylen-phenthiazins. Monatshefte für Chemie - Chemical Monthly. 93(3). 723–732. 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