Hasse Kromann

750 total citations
13 papers, 633 citations indexed

About

Hasse Kromann is a scholar working on Organic Chemistry, Molecular Biology and Toxicology. According to data from OpenAlex, Hasse Kromann has authored 13 papers receiving a total of 633 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Organic Chemistry, 6 papers in Molecular Biology and 4 papers in Toxicology. Recurrent topics in Hasse Kromann's work include Bioactive Compounds and Antitumor Agents (4 papers), Synthesis and biological activity (4 papers) and Pharmacological Effects of Natural Compounds (3 papers). Hasse Kromann is often cited by papers focused on Bioactive Compounds and Antitumor Agents (4 papers), Synthesis and biological activity (4 papers) and Pharmacological Effects of Natural Compounds (3 papers). Hasse Kromann collaborates with scholars based in Denmark, Sweden and Japan. Hasse Kromann's co-authors include Mogens Larsen, Simon Feldbæk Nielsen, Thomas Boesen, Kristian Schønning, Arsalan Kharazmi, Povl Krogsgaard‐Larsen, Marek Treiman, S. Brøgger Christensen, John T. Isaacs and Bertrand Tombal and has published in prestigious journals such as FEBS Letters, Journal of Medicinal Chemistry and Tetrahedron.

In The Last Decade

Hasse Kromann

13 papers receiving 619 citations

Peers

Hasse Kromann

PHARM

TOXIC

CMN

Mogens Larsen Denmark

M Payard France

Abhijit Hazra India

Ram K. Modukuri India

Annalina Lapucci Italy

Subharekha Raghavan United States

Jaime Mella Chile

Maxime Robin France

Anil K. Saxena India

A. GUZMAN Mexico

Mogens Larsen Denmark

Hasse Kromann

581 ×1.4

250 ×1.1

102 ×1.2

PHARM

48 ×0.9

TOXIC

31 ×0.7

CMN

Citations per year, relative to Hasse Kromann Hasse Kromann (= 1×) peers Mogens Larsen

Countries citing papers authored by Hasse Kromann

Since Specialization

Citations

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

Fields of papers citing papers by Hasse Kromann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hasse Kromann

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

All Works

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13 of 13 papers shown

Pelcman, Benjamin, Peter Nilsson, Wesley Schaal, et al.. (2015). 3-Substituted pyrazoles and 4-substituted triazoles as inhibitors of human 15-lipoxygenase-1. Bioorganic & Medicinal Chemistry Letters. 25(15). 3024–3029. 21 indexed citations

Pelcman, Benjamin, Peter Nilsson, Wesley Schaal, et al.. (2015). N-Substituted pyrazole-3-carboxamides as inhibitors of human 15-lipoxygenase. Bioorganic & Medicinal Chemistry Letters. 25(15). 3017–3023. 14 indexed citations

Larsen, Mogens, Hasse Kromann, Arsalan Kharazmi, & Simon Feldbæk Nielsen. (2005). Conformationally restricted anti-plasmodial chalcones. Bioorganic & Medicinal Chemistry Letters. 15(21). 4858–4861. 83 indexed citations

Kromann, Hasse, et al.. (2005). Synthesis of Prenylated Benzaldehydes and Their Use in the Synthesis of Analogues of Licochalcone A.. ChemInform. 36(11). 2 indexed citations

Nielsen, Simon Feldbæk, Mogens Larsen, Thomas Boesen, Kristian Schønning, & Hasse Kromann. (2005). Cationic Chalcone Antibiotics. Design, Synthesis, and Mechanism of Action. Journal of Medicinal Chemistry. 48(7). 2667–2677. 146 indexed citations

Kromann, Hasse, Mogens Larsen, Thomas Boesen, Kristian Schønning, & Simon Feldbæk Nielsen. (2004). Synthesis of prenylated benzaldehydes and their use in the synthesis of analogues of licochalcone A. European Journal of Medicinal Chemistry. 39(11). 993–1000. 30 indexed citations

Nielsen, Simon Feldbæk, Thomas Boesen, Mogens Larsen, Kristian Schønning, & Hasse Kromann. (2004). Antibacterial chalcones––bioisosteric replacement of the 4′-hydroxy group. Bioorganic & Medicinal Chemistry. 12(11). 3047–3054. 155 indexed citations

Kromann, Hasse, Kim Andersen, Povl Krogsgaard‐Larsen, et al.. (2002). Solid-Phase Synthesis of Polyamine Toxin Analogues: Potent and Selective Antagonists of Ca²⁺-Permeable AMPA Receptors. Journal of Medicinal Chemistry. 45(26). 5745–5754. 46 indexed citations

Kromann, Hasse, Frank A. Sløk, Tine B. Stensbøl, et al.. (2002). Selective Antagonists at Group I Metabotropic Glutamate Receptors: Synthesis and Molecular Pharmacology of 4-Aryl-3-isoxazolol Amino Acids. Journal of Medicinal Chemistry. 45(4). 988–991. 6 indexed citations

10.

Stensbøl, Tine B., Peter Uhlmann, Sandrine Morel, et al.. (2001). Novel 1-Hydroxyazole Bioisosteres of Glutamic Acid. Synthesis, Protolytic Properties, and Pharmacology. Journal of Medicinal Chemistry. 45(1). 19–31. 35 indexed citations

11.

Kromann, Hasse, Frank A. Sløk, Tommy N. Johansen, & Povl Krogsgaard‐Larsen. (2001). A convenient synthesis of 4-substituted 3-ethoxy-5-methylisoxazoles by palladium-catalyzed coupling reactions. Tetrahedron. 57(11). 2195–2201. 29 indexed citations

12.

Christensen, S. Brøgger, et al.. (1999). Thapsigargin analogues for targeting programmed death of androgen-Independent prostate cancer cells. Bioorganic & Medicinal Chemistry. 7(7). 1273–1280. 62 indexed citations

13.

Caspersen, Casper, et al.. (1998). ACTA, a fluorescent analogue of thapsigargin, is a potent inhibitor and a conformational probe of skeletal muscle Ca²⁺‐ATPase. FEBS Letters. 439(1-2). 127–132. 4 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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