Janna Velder

1.4k total citations
35 papers, 1.1k citations indexed

About

Janna Velder is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Janna Velder has authored 35 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Organic Chemistry, 13 papers in Molecular Biology and 6 papers in Inorganic Chemistry. Recurrent topics in Janna Velder's work include Synthetic Organic Chemistry Methods (17 papers), Chemical Synthesis and Analysis (8 papers) and Asymmetric Synthesis and Catalysis (6 papers). Janna Velder is often cited by papers focused on Synthetic Organic Chemistry Methods (17 papers), Chemical Synthesis and Analysis (8 papers) and Asymmetric Synthesis and Catalysis (6 papers). Janna Velder collaborates with scholars based in Germany, Russia and Netherlands. Janna Velder's co-authors include Hans‐Günther Schmalz, Tobias Robert, Siegfried Blechert, Heleen Bouman, Christopher M. Waldmann, Dirk Taubert, Christoph Hirschhäuser, Jurriën M. ten Berg, Jochem W. van Werkum and Christian M. Hackeng and has published in prestigious journals such as Angewandte Chemie International Edition, Nature Medicine and Blood.

In The Last Decade

Janna Velder

34 papers receiving 1.1k citations

Peers

Countries citing papers authored by Janna Velder

Since Specialization

Citations

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

Fields of papers citing papers by Janna Velder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janna Velder

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Total Synthesis of (2RS)‐α‐Tocopherol through Ni‐Catalyzed 1,4‐Addition to a Chromenone Intermediate 2014 ·European Journal of Organic Chemistry ·(unknown), Janna Velder, René T. Stemmler, Thomas Netscher, Werner Bonrath, Hans‐Günther Schmalz	10
2	Lipophilic prodrugs of a triazole-containing colchicine analogue in liposomes: Biological effects on human tumor cells 2013 ·Russian Journal of Bioorganic Chemistry ·(unknown), E. V. Svirshchevskaya, Nikolay S. Sitnikov, (unknown), (unknown), (unknown), Janna Velder, (unknown), Hartmut Oschkinat, Aram Prokop, Hans‐Günther Schmalz, Alexey Yu. Fedorov, Е. Л. Водовозова	27
3	Total Synthesis of Indole‐Derived Allocolchicine Analogues Exhibiting Strong Apoptosis‐Inducing Activity 2012 ·Chemistry - A European Journal ·Nikolay S. Sitnikov, Janna Velder, (unknown), (unknown), Jörg‐M. Neudörfl, Aram Prokop, Günter Krause, Alexey Yu. Fedorov, Hans‐Günther Schmalz	29
4	Reply to: "Paraoxonase-1 and clopidogrel efficacy" 2011 ·Nature Medicine ·Heleen Bouman, Edgar Schömig, Jochem W. van Werkum, Janna Velder, Christian M. Hackeng, Christoph Hirschhäuser, Christopher M. Waldmann, Hans‐Günther Schmalz, Jurriën M. ten Berg, Dirk Taubert	6
5	Paraoxonase-1 is a major determinant of clopidogrel efficacy 2010 ·Nature Medicine ·Heleen Bouman, Edgar Schömig, Jochem W. van Werkum, Janna Velder, Christian M. Hackeng, Christoph Hirschhäuser, Christopher M. Waldmann, Hans‐Günther Schmalz, Jurriën M. ten Berg, Dirk Taubert	356
6	Anti‐inflammatory AreneChromium Complexes Acting as Specific Inhibitors of NOD2 Signalling 2010 ·ChemMedChem ·(unknown), Janna Velder, (unknown), (unknown), (unknown), Wiltrud M. Kalka-Moll, Martin Krönke, Hans‐Günther Schmalz, Thomas A. Kufer	28
7	A Scalable Synthesis of (±)-2-Oxoclopidogrel 2010 ·Synlett ·Hans‐Günther Schmalz, Janna Velder, Christoph Hirschhäuser, Christopher M. Waldmann, Dirk Taubert, Heleen Bouman	2
8	A Convenient Entry to New C-7-Modified Colchicinoids through Azide Alkyne [3+2] Cycloaddition: Application of Ring-Contractive Rearrangements 2010 ·Heterocycles ·Hans‐Günther Schmalz, Norman Nicolaus, (unknown), Nikolay S. Sitnikov, Alexey Yu. Fedorov, Janna Velder, (unknown)	32
9	trans-Ethylenedi-p-phenylene diacetate 2009 ·Acta Crystallographica Section E Structure Reports Online ·Stefanie Ritter, Jörg‐M. Neudörfl, Janna Velder, Hans‐Günther Schmalz	1
10	Enantioselective Cu‐Catalyzed 1,4‐Addition of Grignard Reagents to Cyclohexenone Using Taddol‐Derived Phosphine–Phosphite Ligands and 2‐Methyl‐THF as a Solvent 2008 ·Angewandte Chemie International Edition ·Tobias Robert, Janna Velder, Hans‐Günther Schmalz	96
11	Synthesis of a Mumbaistatin Analogue through Cross-Coupling 2007 ·Synlett ·Hans‐Günther Schmalz, David Sucunza, (unknown), (unknown), Janna Velder, Johann Lex	3
12	Gram-scale synthesis of pinusolide and evaluation of its antileukemic potential 2006 ·Bioorganic & Medicinal Chemistry Letters ·Elvira E. Shults, Janna Velder, Hans‐Günther Schmalz, S. V. Chernov, (unknown), Yu. V. Gatilov, G. Henze, Г. А. Толстиков, Aram Prokop	34
13	A Simple Access to Biologically Importanttrans-Stilbenes via Ru-Catalyzed Cross Metathesis 2006 ·Synthesis ·Hans‐Günther Schmalz, Janna Velder, Stefanie Ritter, Johann Lex	2
14	New Pinostilbene Analogues Overcome Anthracycline Resistance in Acute Lymphoplastic Leukemia Ex Vivo. 2006 ·Blood ·(unknown), (unknown), Janna Velder, Elvira E. Shults, Thomas Wieder, Guenter Henze, Hans‐Günther Schmalz, Aram Prokop	1
15	A Simple Access to Biologically Important trans‐Stilbenes via Ru‐Catalyzed Cross Metathesis. 2006 ·ChemInform ·Janna Velder, Stefanie Ritter, Johann Lex, Hans‐Günther Schmalz	2
16	Si(CH2CH2SnH3)4—a unique organotin hydride featuring 12 SnH units in a dendritic molecule. Single-crystal X-ray structures of tetrakis(2-stannylethylene)silane and tetrakis[2-(triphenylstannyl)ethylene]silane 2000 ·Journal of Organometallic Chemistry ·Herbert Schumann, B.C. Wassermann, (unknown), Bamidele A. Omotowa, S. Schutte, Janna Velder, S.H. Muhle, W. Kŕause	22
17	Selective Ring‐Opening Olefin Metathesis of Functionalized Monosubstituted Olefins 1997 ·Angewandte Chemie International Edition in English ·Matthias Schneider, (unknown), Janna Velder, Siegfried Blechert	68
18	Selektive ringöffnende Olefinmetathese mit funktionalisierten monosubstituierten Olefinen 1997 ·Angewandte Chemie ·Matthias Schneider, (unknown), Janna Velder, Siegfried Blechert	23
19	A Catalyst‐Specific, Stereocontrolled Ring‐Closing Metathesis 1996 ·Angewandte Chemie International Edition in English ·Christoph M. Huwe, Janna Velder, Siegfried Blechert	63
20	Eine katalysatorspezifische, stereokontrollierte Ringschlußmetathese 1996 ·Angewandte Chemie ·Christoph M. Huwe, Janna Velder, Siegfried Blechert	20

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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