Jens‐Peter Steffen

533 total citations
18 papers, 451 citations indexed

About

Jens‐Peter Steffen is a scholar working on Organic Chemistry, Molecular Biology and Complementary and alternative medicine. According to data from OpenAlex, Jens‐Peter Steffen has authored 18 papers receiving a total of 451 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 5 papers in Molecular Biology and 1 paper in Complementary and alternative medicine. Recurrent topics in Jens‐Peter Steffen's work include Cyclization and Aryne Chemistry (10 papers), Catalytic Alkyne Reactions (10 papers) and Chemical synthesis and alkaloids (4 papers). Jens‐Peter Steffen is often cited by papers focused on Cyclization and Aryne Chemistry (10 papers), Catalytic Alkyne Reactions (10 papers) and Chemical synthesis and alkaloids (4 papers). Jens‐Peter Steffen collaborates with scholars based in Germany and Spain. Jens‐Peter Steffen's co-authors include Michael Schmittel, David Rodrı́guez, Bernd Engels, Christian Lennartz, Michael Hanrath, Peter Schreier, Markus Herderich, Wilfried Schwab, Dominik Auer and Holger Helten and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and Journal of Agricultural and Food Chemistry.

In The Last Decade

Jens‐Peter Steffen

18 papers receiving 441 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jens‐Peter Steffen Germany 11 352 137 29 26 25 18 451
Marta Sališová Slovakia 10 174 0.5× 68 0.5× 39 1.3× 49 1.9× 32 1.3× 36 341
Alexander E. A. Porter United Kingdom 10 215 0.6× 90 0.7× 34 1.2× 13 0.5× 8 0.3× 30 311
John Almy United States 11 172 0.5× 74 0.5× 39 1.3× 62 2.4× 16 0.6× 32 312
Wolfgang Neugebauer Germany 10 246 0.7× 41 0.3× 23 0.8× 55 2.1× 27 1.1× 16 375
И. В. Федорова Russia 12 231 0.7× 154 1.1× 66 2.3× 10 0.4× 66 2.6× 67 430
Kenji Makino Japan 13 305 0.9× 67 0.5× 121 4.2× 23 0.9× 5 0.2× 29 562
Marco Boccalini Italy 13 372 1.1× 114 0.8× 56 1.9× 8 0.3× 15 0.6× 23 483
Jean‐Pierre Zahra France 11 229 0.7× 91 0.7× 26 0.9× 14 0.5× 3 0.1× 36 333
Tomonori Katada Japan 12 242 0.7× 47 0.3× 7 0.2× 20 0.8× 31 1.2× 31 359
P. H. MCCABE United Kingdom 11 164 0.5× 101 0.7× 100 3.4× 11 0.4× 9 0.4× 30 338

Countries citing papers authored by Jens‐Peter Steffen

Since Specialization
Citations

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

Fields of papers citing papers by Jens‐Peter Steffen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jens‐Peter Steffen. 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 Jens‐Peter Steffen. The network helps show where Jens‐Peter Steffen may publish in the future.

Co-authorship network of co-authors of Jens‐Peter Steffen

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

All Works

18 of 18 papers shown
1.
Schmittel, Michael, Jens‐Peter Steffen, David Rodrı́guez, et al.. (2008). Thermal C2−C6Cyclization of Enyne−Carbodiimides:  Experimental Evidence Contradicts a Diradical and Suggests a Carbene Intermediate. The Journal of Organic Chemistry. 73(8). 3005–3016. 31 indexed citations
2.
Gross, Julia Christina, et al.. (2006). Combination of TLC and HPLC-MS/MS Methods. Approach to a Rational Quality Control of Chinese Star Anise. Journal of Agricultural and Food Chemistry. 54(6). 1970–1974. 24 indexed citations
3.
Schmittel, Michael, et al.. (2004). A New Facile Synthesis ofexo-Methylene 3,1-Benzothiazines. Synthesis. 415–418. 20 indexed citations
4.
Schmittel, Michael, et al.. (2001). Ring size effects in the C2–C6 biradical cyclisation of enyne–allenes and the relevance for neocarzinostatin. Journal of the Chemical Society Perkin Transactions 2. 1331–1339. 34 indexed citations
5.
Schmittel, Michael, David Rodrı́guez, & Jens‐Peter Steffen. (2000). A Highly Efficient Triplet Analogue of a Thermal Biradical Cyclization—The Photochemical C2-C6 Cyclization of Enyne-Heteroallenes. Angewandte Chemie International Edition. 39(12). 2152–2155. 63 indexed citations
6.
Schmittel, Michael, David Rodrı́guez, & Jens‐Peter Steffen. (2000). A Highly Efficient Triplet Analogue of a Thermal Biradical Cyclization—The Photochemical C2–C6 Cyclization of Enyne-Heteroallenes. Angewandte Chemie. 112(12). 2236–2239. 8 indexed citations
7.
Schmittel, Michael, David Rodrı́guez, & Jens‐Peter Steffen. (2000). Synthesis and Photochemical Cyclization of a Novel Enyne-Carbodiimide. Molecules. 5(12). 1372–1378. 9 indexed citations
8.
Schmittel, Michael, Jens‐Peter Steffen, Armin Burghart, et al.. (1999). First Characterization of Phosphoenol Radical Cations in Solution and the Kinetics of the Mesolytic P--O Bond Cleavage in Sterically Shielded Enoxy-Phosphorus Compounds after One-Electron Oxidation.. Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry. 53. 781–791. 7 indexed citations
9.
Schmittel, Michael, Jens‐Peter Steffen, Bernd Engels, Christian Lennartz, & Michael Hanrath. (1998). Two Novel Thermal Biradical Cyclizations in Theory and Experiment: New Synthetic Routes to 6H-Indolo[2,3-b]quinolines and 2-Aminoquinolines from Enyne-Carbodiimides. Angewandte Chemie International Edition. 37(17). 2371–2373. 53 indexed citations
10.
Schmittel, Michael, et al.. (1998). Two Novel Thermal Biradical Cyclizations of Enyne-Ketenimines: Theory, Experiment, and Synthetic Potential. Angewandte Chemie International Edition. 37(11). 1562–1564. 54 indexed citations
11.
Schmittel, Michael, Jens‐Peter Steffen, Bernd Engels, Christian Lennartz, & Michael Hanrath. (1998). Zwei neue thermische Diradikal-Cyclisierungen in Theorie und Experiment: neue Syntheserouten zu 6H-Indolo[2,3-b]chinolinen und 2-Aminochinolinen aus Enincarbodiimiden. Angewandte Chemie. 110(17). 2531–2533. 12 indexed citations
12.
Schmittel, Michael, et al.. (1998). Zwei neue thermische Diradikal- Cyclisierungen von Eninketeniminen: Theorie, Experiment und Synthesepotential. Angewandte Chemie. 110(11). 1633–1635. 17 indexed citations
14.
Schmittel, Michael, et al.. (1997). Ring Strain Effects in Enyne-Allene Thermolysis: Switch from the Myers-Saito Reaction to the C2-C6 Biradical Cyclization. Tetrahedron Letters. 38(35). 6177–6180. 44 indexed citations
16.
Herderich, Markus, et al.. (1996). 2,5-Dimethyl-4-hydroxy-3[2H]-furanone 6′O-malonyl-β-d-glucopyranoside in strawberry fruits. Phytochemistry. 43(1). 155–159. 52 indexed citations
17.
Steffen, Jens‐Peter, et al.. (1996). Synthesis of Phenyl 6‘-O-Malonyl-β-d-glucopyranoside. Facile Preparation of Malonylated Glycoconjugates. Journal of Agricultural and Food Chemistry. 44(7). 1626–1629. 9 indexed citations
18.
Schmittel, Michael, Jens‐Peter Steffen, & Armin Burghart. (1996). One-electron oxidation of enol phosphates, enol phosphites and enol phosphinates. Evidence for an unprecedented P–O bond cleavage in phosphoenol radical cations in solution1. Chemical Communications. 2349–2350. 7 indexed citations

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