H. SCHOENENBERGER

772 total citations
28 papers, 651 citations indexed

About

H. SCHOENENBERGER is a scholar working on Organic Chemistry, Oncology and Genetics. According to data from OpenAlex, H. SCHOENENBERGER has authored 28 papers receiving a total of 651 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Organic Chemistry, 9 papers in Oncology and 7 papers in Genetics. Recurrent topics in H. SCHOENENBERGER's work include Metal complexes synthesis and properties (9 papers), Estrogen and related hormone effects (7 papers) and Synthesis and Reactions of Organic Compounds (6 papers). H. SCHOENENBERGER is often cited by papers focused on Metal complexes synthesis and properties (9 papers), Estrogen and related hormone effects (7 papers) and Synthesis and Reactions of Organic Compounds (6 papers). H. SCHOENENBERGER collaborates with scholars based in Germany, Switzerland and Australia. H. SCHOENENBERGER's co-authors include Erwin von Angerer, Rolf W. Hartmann, Ronald Gust, Martin R. Schneider, Thomas Burgemeister, Albrecht Mannschreck, Juergen Engel, G. Ruckdeschel, Patrick J. Bednarski and M. R. Schneider and has published in prestigious journals such as Journal of Medicinal Chemistry, Inorganic Chemistry and Chemische Berichte.

In The Last Decade

H. SCHOENENBERGER

27 papers receiving 634 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H. SCHOENENBERGER Germany 15 497 279 181 168 56 28 651
Helmut Schönenberger Germany 16 677 1.4× 626 2.2× 157 0.9× 214 1.3× 86 1.5× 89 944
G. Rihs Switzerland 13 211 0.4× 96 0.3× 57 0.3× 128 0.8× 69 1.2× 23 546
Jacques I. Quivy Belgium 7 458 0.9× 272 1.0× 83 0.5× 191 1.1× 22 0.4× 14 629
William M. Scovell United States 17 228 0.5× 305 1.1× 83 0.5× 449 2.7× 94 1.7× 42 803
Anthony D. Sercel United States 14 612 1.2× 118 0.4× 18 0.1× 389 2.3× 21 0.4× 27 901
Masahide Noji Japan 14 303 0.6× 343 1.2× 53 0.3× 287 1.7× 72 1.3× 44 708
U. K. PANDIT Netherlands 18 761 1.5× 43 0.2× 38 0.2× 414 2.5× 72 1.3× 111 1.1k
Hermann Künzer Germany 11 274 0.6× 45 0.2× 57 0.3× 154 0.9× 36 0.6× 36 418
M.R. Díaz Spain 17 587 1.2× 107 0.4× 32 0.2× 196 1.2× 219 3.9× 62 790
Suzy Cros France 13 277 0.6× 336 1.2× 14 0.1× 235 1.4× 77 1.4× 17 585

Countries citing papers authored by H. SCHOENENBERGER

Since Specialization
Citations

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

Fields of papers citing papers by H. SCHOENENBERGER

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. SCHOENENBERGER

This figure shows the co-authorship network connecting the top 25 collaborators of H. SCHOENENBERGER. A scholar is included among the top collaborators of H. SCHOENENBERGER 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 H. SCHOENENBERGER. H. SCHOENENBERGER 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
3.
Bednarski, Patrick J., et al.. (1992). Diamine ligand release from the cisplatin analog [meso-1,2-bis(2,6-dichloro-4-hydroxyphenyl)ethylenediamine]dichloroplatinum(II) in cell culture medium. Journal of Medicinal Chemistry. 35(23). 4479–4485. 13 indexed citations
5.
Gust, Ronald, Thomas Burgemeister, Albrecht Mannschreck, & H. SCHOENENBERGER. (1990). Aqua[1-(2,6-dichloro-4-hydroxyphenyl)-2-phenylethylenediamine](sulfato)platinum(II) complexes with variable substituents in the 2-phenyl ring. 1. Synthesis and antitumor and estrogenic properties. Journal of Medicinal Chemistry. 33(9). 2535–2544. 64 indexed citations
6.
Gust, Ronald, Thilo Spruß, M. R. Schneider, et al.. (1988). Ring-substituted [1,2-bis(4-hydroxyphenyl)ethylenediamine]dichloroplatinum(II) complexes: compounds with a selective effect on the hormone-dependent mammary carcinoma. Journal of Medicinal Chemistry. 31(1). 72–83. 80 indexed citations
7.
Hartmann, Rolf W., et al.. (1986). Influence of alkyl-chain fluorination on the action of mammary tumor inhibiting 2,3-bis(hydroxyphenyl)butanes and 2,3-bis(hydroxyphenyl)but-2-enes. Journal of Medicinal Chemistry. 29(3). 322–328. 16 indexed citations
8.
Schneider, Martin R., et al.. (1985). Acetoxy-substituted 1,1,2-triphenylbut-1-enes with antiestrogenic and mammary tumor inhibiting properties. Journal of Medicinal Chemistry. 28(12). 1880–1885. 33 indexed citations
9.
Angerer, Erwin von, et al.. (1984). Benzylamines: synthesis and evaluation of antimycobacterial properties. Journal of Medicinal Chemistry. 27(9). 1111–1118. 55 indexed citations
11.
Hartmann, Rolf W., Walter Schwarz, & H. SCHOENENBERGER. (1983). Ring-substituted 1,2-dialkylated 1,2-bis(hydroxyphenyl)ethanes. 1. Synthesis and estrogen receptor binding affinity of 2,2'- and 3,3'-disubstituted hexestrols. Journal of Medicinal Chemistry. 26(8). 1137–1144. 9 indexed citations
12.
Hartmann, Robert, Wolfgang H. Schwarz, & H. SCHOENENBERGER. (1983). ChemInform Abstract: RING‐SUBSTITUTED 1,2‐DIALKYLATED 1,2‐BIS(HYDROXYPHENYL)ETHANES. 1. SYNTHESIS AND ESTROGEN RECEPTOR BINDING AFFINITY OF 2,2′‐ AND 3,3′‐DISUBSTITUTED HEXESTROLS. Chemischer Informationsdienst. 14(50). 2 indexed citations
13.
Schneider, Martin R., Erwin von Angerer, & H. SCHOENENBERGER. (1982). ChemInform Abstract: 5‐ACETOXY‐2‐(3‐ACETOXYPHENYL)‐3‐ETHYL‐1‐METHYL‐1H‐INDENE: A NEW MAMMARY TUMOR INHIBITING COMPOUND. Chemischer Informationsdienst. 13(39). 1 indexed citations
14.
Schneider, Martin R., et al.. (1982). Mammary tumor inhibiting effect of 3,3'-diacetoxy-.alpha.,.beta.-dialkylstilbenes and of related stilbene oxides. Journal of Medicinal Chemistry. 25(2). 141–145. 12 indexed citations
16.
Hartmann, Rolf W., et al.. (1981). Potential antiestrogens. Synthesis and evaluation of mammary tumor inhibiting activity of 1,2-dialkyl-1,2-bis(3'-hydroxyphenyl)ethanes. Journal of Medicinal Chemistry. 24(10). 1192–1197. 18 indexed citations
17.
Hartmann, Rolf W., et al.. (1980). Antiestrogens. Synthesis and evaluation of mammary tumor inhibiting activity of 1,1,2,2-tetraalkyl-1,2-diphenylethanes. Journal of Medicinal Chemistry. 23(8). 841–848. 54 indexed citations
19.
SCHOENENBERGER, H. & Turgut Baştuğ. (1970). β-アミノケトン類の物理化学的性質と抗菌作用の関係 IX 細胞静止薬. 20(3). 386–390.
20.
SCHOENENBERGER, H., et al.. (1956). Über die Reaktion von Grignard‐Verbindungen mit Schiffschen Basen, I. Mitteil.: Die Bildung von Äthylendiaminderivaten. Chemische Berichte. 89(8). 1918–1921. 24 indexed citations

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