Marion Slopianka

454 total citations
32 papers, 346 citations indexed

About

Marion Slopianka is a scholar working on Organic Chemistry, Molecular Biology and Physical and Theoretical Chemistry. According to data from OpenAlex, Marion Slopianka has authored 32 papers receiving a total of 346 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Organic Chemistry, 7 papers in Molecular Biology and 4 papers in Physical and Theoretical Chemistry. Recurrent topics in Marion Slopianka's work include Synthesis and Reactions of Organic Compounds (5 papers), Synthesis of heterocyclic compounds (4 papers) and Steroid Chemistry and Biochemistry (4 papers). Marion Slopianka is often cited by papers focused on Synthesis and Reactions of Organic Compounds (5 papers), Synthesis of heterocyclic compounds (4 papers) and Steroid Chemistry and Biochemistry (4 papers). Marion Slopianka collaborates with scholars based in Germany and United States. Marion Slopianka's co-authors include Wolfgang Sucrow, Eckehard V. Dehmlow, Henry W. Kircher, Albert Gossauer, Joachim Pickardt, Walter Lwowski, Steven W. Lockley, D. Winkler, Günther Snatzke and Reinhard Zeisberg and has published in prestigious journals such as Phytochemistry, Tetrahedron Letters and Chemische Berichte.

In The Last Decade

Marion Slopianka

30 papers receiving 315 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marion Slopianka Germany 11 232 122 39 26 23 32 346
Charles M. Buess United States 13 163 0.7× 98 0.8× 44 1.1× 6 0.2× 14 0.6× 25 308
Toshio Hoshino Japan 7 491 2.1× 207 1.7× 30 0.8× 90 3.5× 8 0.3× 13 581
N. INUKAI Japan 12 216 0.9× 177 1.5× 43 1.1× 35 1.3× 3 0.1× 27 334
Kentaro Okumura United States 11 254 1.1× 109 0.9× 19 0.5× 9 0.3× 6 0.3× 36 333
Mark S. Cooper United Kingdom 5 275 1.2× 103 0.8× 27 0.7× 16 0.6× 4 0.2× 6 378
Thomas F. Brennan United States 11 187 0.8× 77 0.6× 24 0.6× 4 0.2× 14 0.6× 17 340
Richard W. Thies United States 10 207 0.9× 67 0.5× 18 0.5× 16 0.6× 2 0.1× 34 264
A. M. Moiseenkov Russia 7 211 0.9× 83 0.7× 28 0.7× 15 0.6× 2 0.1× 98 278
Jitendra A. Sattigeri India 12 226 1.0× 136 1.1× 12 0.3× 5 0.2× 22 1.0× 30 369
Gerhard Rembarz Germany 10 331 1.4× 168 1.4× 13 0.3× 30 1.2× 4 0.2× 54 391

Countries citing papers authored by Marion Slopianka

Since Specialization
Citations

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

Fields of papers citing papers by Marion Slopianka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marion Slopianka

This figure shows the co-authorship network connecting the top 25 collaborators of Marion Slopianka. A scholar is included among the top collaborators of Marion Slopianka 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 Marion Slopianka. Marion Slopianka 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.
Dehmlow, Eckehard V. & Marion Slopianka. (2006). Vakuumpyrolyse von 5,5,10,10-Tetrachlortricyclo[7.1.0.04,6]deca-2,7-dien: 1,5- und 2,6-Dichlorazulene. Angewandte Chemie. 94(6). 461–461. 1 indexed citations
2.
Slopianka, Marion & Albert Gossauer. (1981). Thiocarbonyl‐Olefinierung, IV. Darstellung von β‐Aminosäuren aus N‐(Acetyl)thioamiden; Totalsynthese der Iturinsäure. Liebigs Annalen der Chemie. 1981(12). 2258–2265. 10 indexed citations
3.
Slopianka, Marion & Albert Gossauer. (1981). Thiocarbonyl Olefination III1: A New Synthesis of β-Aminoacids from N-Thioacylurethanes. Synthetic Communications. 11(2). 95–99. 4 indexed citations
4.
Dehmlow, Eckehard V. & Marion Slopianka. (1979). Blitzthermolyse von doppelt ungesättigten Säurehalogeniden zu Phenolen. Angewandte Chemie. 91(2). 163–163. 2 indexed citations
5.
Dehmlow, Eckehard V., Marion Slopianka, & Joachim Pickardt. (1979). Stereochemie der Dimerisierung von unsymmetrisch substituierten Ketoketenen. Liebigs Annalen der Chemie. 1979(4). 572–593. 8 indexed citations
6.
Sucrow, Wolfgang & Marion Slopianka. (1978). ChemInform Abstract: ENEHYDRAZINES, 19. PYRAZOLIUM BETAINES FROM 1,1‐DIALKYLHYDRAZINES AND ACETYLENECARBOXYLIC ESTERS. Chemischer Informationsdienst. 9(15). 1 indexed citations
7.
Sucrow, Wolfgang, et al.. (1978). Enhydrazine, 20: Pyrazolinium‐Betaine aus 1,1‐Dimethylhydrazin und 3‐Phenylglycidsäureestern. Chemische Berichte. 111(2). 791–796. 5 indexed citations
8.
Dehmlow, Eckehard V., et al.. (1977). Phase transfer catalysis in strongly alkaline media : notes on the extractability of hydroxyl ions and on the stability of catalysts.. Tetrahedron Letters. 18(27). 2361–2364. 31 indexed citations
9.
Sucrow, Wolfgang, Marion Slopianka, & Henry W. Kircher. (1976). The occurrence of C29 sterols with different configurations at C-24 in Cucurbita Pepo as shown by 270 MHz NMR. Phytochemistry. 15(10). 1533–1535. 52 indexed citations
10.
Slopianka, Marion, et al.. (1976). ChemInform Abstract: ENEHYDRAZINES, 11. STRUCTURE AND REACTIONS OF DIMETHYL 2‐(1‐METHYLHYDRAZINO)MALEATE. Chemischer Informationsdienst. 7(8). 1 indexed citations
11.
Sucrow, Wolfgang, et al.. (1975). Stable Pyrazolium Betaines by Addition of 1,1‐Dialkyl‐hydrazines to Acetylenecarboxylic Esters. Angewandte Chemie International Edition in English. 14(8). 560–561. 8 indexed citations
12.
Sucrow, Wolfgang & Marion Slopianka. (1975). β‐Sitosterin und Clionasterin aus (24R)‐ bzw. (24S)‐24‐Äthylcholesta‐5,22,25‐trien‐3β‐ol. Chemische Berichte. 108(12). 3721–3729. 5 indexed citations
13.
Slopianka, Marion, et al.. (1975). Stabile Pyrazolium‐Betaine durch Addition von 1,1‐Dialkylhydrazinen an Acetylencarbonsäureester. Angewandte Chemie. 87(15). 551–551. 5 indexed citations
14.
15.
Sucrow, Wolfgang, et al.. (1973). Enhydrazine, 61) Weitere Enhydrazone, Tetrahydroindazolone und Enhydrazine aus cyclischen β‐Dicarbonylverbindungen. Chemische Berichte. 106(2). 450–459. 15 indexed citations
16.
Sucrow, Wolfgang, et al.. (1973). Enhydrazine, 8. Einige neue Indazol‐Derivate. Chemische Berichte. 106(10). 3432–3437. 5 indexed citations
17.
Sucrow, Wolfgang, et al.. (1973). Enhydrazine, 7. Carbazolderivate aus Enhydrazinen. Chemische Berichte. 106(3). 745–750. 9 indexed citations
18.
Sucrow, Wolfgang, Marion Slopianka, & D. Winkler. (1972). Hydroxyalkylierung von Carbonsäure‐dialkylamiden mit Epoxiden. Chemische Berichte. 105(5). 1621–1633. 10 indexed citations
19.
Sucrow, Wolfgang, et al.. (1971). Stereochemie einer Claisen‐Umlagerung in der Sterin‐Seitenkette. Chemische Berichte. 104(11). 3689–3703. 40 indexed citations
20.
Sucrow, Wolfgang, et al.. (1971). Zur konfiguration der stigmastatrien-(5 bzw.7.22.25)-ole-(3β). Tetrahedron Letters. 12(35). 3237–3240. 3 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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