Willi Kantlehner

2.3k total citations
177 papers, 1.7k citations indexed

About

Willi Kantlehner is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Willi Kantlehner has authored 177 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 158 papers in Organic Chemistry, 68 papers in Molecular Biology and 27 papers in Inorganic Chemistry. Recurrent topics in Willi Kantlehner's work include Chemical Synthesis and Analysis (65 papers), Synthesis of heterocyclic compounds (45 papers) and Chemical Synthesis and Reactions (42 papers). Willi Kantlehner is often cited by papers focused on Chemical Synthesis and Analysis (65 papers), Synthesis of heterocyclic compounds (45 papers) and Chemical Synthesis and Reactions (42 papers). Willi Kantlehner collaborates with scholars based in Germany, Bulgaria and United States. Willi Kantlehner's co-authors include Hellmut Bredereck, Edmont Stoyanov, Jochen Mezger, Erwin Haug, Michaël Grätzel, Shaik M. Zakeeruddin, Gerhard Simchen, Peng Wang, Robin Humphry‐Baker and Bernard Wenger and has published in prestigious journals such as Journal of the American Chemical Society, SHILAP Revista de lepidopterología and Chemistry of Materials.

In The Last Decade

Willi Kantlehner

169 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Willi Kantlehner Germany 19 1.1k 340 334 273 247 177 1.7k
Sofja Tshepelevitsh Estonia 13 676 0.6× 222 0.7× 103 0.3× 203 0.7× 177 0.7× 42 1.3k
Shu‐Ping Luo China 32 2.1k 1.8× 247 0.7× 382 1.1× 524 1.9× 770 3.1× 76 3.1k
Koichi Mitsudo Japan 29 2.1k 1.9× 273 0.8× 81 0.2× 239 0.9× 153 0.6× 115 2.4k
Francesco Recupero Italy 26 2.2k 1.9× 103 0.3× 272 0.8× 673 2.5× 203 0.8× 50 2.6k
Maurice Médebielle France 36 2.8k 2.5× 314 0.9× 104 0.3× 177 0.6× 147 0.6× 121 3.8k
Mohammed Bakir Jamaica 20 633 0.6× 70 0.2× 130 0.4× 314 1.2× 246 1.0× 82 1.4k
Shengchun Wang China 33 2.9k 2.6× 259 0.8× 109 0.3× 223 0.8× 459 1.9× 82 3.5k
Carl Christoph Tzschucke Germany 24 1.3k 1.2× 327 1.0× 161 0.5× 173 0.6× 53 0.2× 46 1.7k
Chhanda Mukhopadhyay India 28 2.5k 2.2× 510 1.5× 105 0.3× 340 1.2× 59 0.2× 190 2.9k
James Grimshaw United Kingdom 20 603 0.5× 270 0.8× 65 0.2× 312 1.1× 167 0.7× 94 1.4k

Countries citing papers authored by Willi Kantlehner

Since Specialization
Citations

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

Fields of papers citing papers by Willi Kantlehner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Willi Kantlehner

This figure shows the co-authorship network connecting the top 25 collaborators of Willi Kantlehner. A scholar is included among the top collaborators of Willi Kantlehner 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 Willi Kantlehner. Willi Kantlehner 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
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Kantlehner, Willi, et al.. (2022). Orthoamide und Iminiumsalze, CVIa. Kondensationsreaktionen von Orthoamiden der Alkincarbonsäuren mit CH-aciden Methylheterocyclen. Zeitschrift für Naturforschung B. 77(10). 743–755. 2 indexed citations
3.
Kantlehner, Willi, Jochen Mezger, Jean Sommer, et al.. (2019). Zur Formylierung von Hydroxy- und Alkoxyaromaten mit Ameisensäure. Zeitschrift für Naturforschung B. 74(10). 709–732. 1 indexed citations
4.
Kantlehner, Willi, et al.. (2018). Orthoamide und Iminiumsalze, XCII. Synthese und Reaktionen von Orthoamiden aus ethinylierten Terpenderivatena. Zeitschrift für Naturforschung B. 73(7). 437–455. 8 indexed citations
5.
Tiritiris, Ioannis & Willi Kantlehner. (2015). Crystal structure ofN,N,N′,N′,N′′,N′′-hexamethylguanidinium cyanate 1.5-hydrate. SHILAP Revista de lepidopterología. 71(12). o1076–o1077. 1 indexed citations
6.
Tiritiris, Ioannis & Willi Kantlehner. (2015). Crystal structure of 2-dimethylamino-1-ethoxycarbonyl-3-methyl-3,4,5,6-tetrahydropyrimidin-1-ium tetraphenylborate. SHILAP Revista de lepidopterología. 71(11). o894–o895. 2 indexed citations
7.
Tiritiris, Ioannis & Willi Kantlehner. (2015). Crystal structure ofN-[3-(dimethylamino)propyl]-N′,N′,N′′,N′′-tetramethyl-N-(N,N,N′,N′-tetramethylformamidiniumyl)guanidinium bis(tetraphenylborate). SHILAP Revista de lepidopterología. 71(12). o1045–o1046. 2 indexed citations
8.
Tiritiris, Ioannis & Willi Kantlehner. (2015). Crystal structure ofN-[3-(dimethylazaniumyl)propyl]-N′,N′,N′′,N′′-tetramethyl-N-(N,N,N′,N′-tetramethylformamidiniumyl)guanidinium dibromide hydroxide monohydrate. SHILAP Revista de lepidopterología. 71(12). o1078–o1079. 1 indexed citations
9.
Tiritiris, Ioannis & Willi Kantlehner. (2015). Crystal structure ofN′′-(2-ethoxy-2-oxoethyl)-N,N,N′,N′-tetramethyl-N′′-[3-(1,3,3-trimethylureido)propyl]guanidinium tetraphenylborate. SHILAP Revista de lepidopterología. 71(12). o1026–o1027. 1 indexed citations
10.
Tiritiris, Ioannis, et al.. (2014). (Methoxymethylidene)dimethylazanium tetraphenylborate acetonitrile monosolvate. Acta Crystallographica Section E Structure Reports Online. 70(3). o333–o333. 2 indexed citations
11.
Tiritiris, Ioannis, Wolfgang Frey, & Willi Kantlehner. (2014). N′′-(4-Methoxyphenyl)-N,N,N′-trimethyl-N′-phenylguanidine. Acta Crystallographica Section E Structure Reports Online. 70(4). o460–o460.
12.
Tiritiris, Ioannis & Willi Kantlehner. (2013). 2-[4-(Carbazol-9-yl)phenyl]-1,3-diethyl-1,3-diphenylguanidine. Acta Crystallographica Section E Structure Reports Online. 69(7). o1066–o1066. 1 indexed citations
13.
Spitzner, D., et al.. (2012). Synthesis and Characterization of Chiral Guanidines und Guanidinium Salts Derived from 1-Phenylethylamine. Zeitschrift für Naturforschung B. 67(4). 337–346. 6 indexed citations
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Sauer, Sven, Stefan Tussetschläger, Angelika Baro, et al.. (2009). p-Alkoxybiphenyls with guanidinium head groups displaying smectic mesophases. Liquid Crystals. 36(3). 275–299. 32 indexed citations
17.
Bogdanov, Milen G., Boyan Iliev, & Willi Kantlehner. (2009). The Residual Volume Approach II: Simple Prediction of Ionic Conductivity of Ionic Liquids. Zeitschrift für Naturforschung B. 64(6). 756–764. 18 indexed citations
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Bagno, Alessandro, et al.. (2001). New Formylating Agents − Preparative Procedures and Mechanistic Investigations. European Journal of Organic Chemistry. 2001(15). 2947–2947. 10 indexed citations
20.
Kantlehner, Willi, et al.. (1982). Notiz zur Darstellung N,N‐disubstituierter aliphatischer Thiocarbonsäureamide, N‐substituierter Thiolactame und aromatischer Thiocarbonsäureester. Liebigs Annalen der Chemie. 1982(8). 1582–1587. 6 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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