Axel Monsees

1.9k total citations
45 papers, 1.6k citations indexed

About

Axel Monsees is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Axel Monsees has authored 45 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Organic Chemistry, 35 papers in Inorganic Chemistry and 13 papers in Molecular Biology. Recurrent topics in Axel Monsees's work include Asymmetric Hydrogenation and Catalysis (34 papers), Asymmetric Synthesis and Catalysis (15 papers) and Chemical Synthesis and Analysis (11 papers). Axel Monsees is often cited by papers focused on Asymmetric Hydrogenation and Catalysis (34 papers), Asymmetric Synthesis and Catalysis (15 papers) and Chemical Synthesis and Analysis (11 papers). Axel Monsees collaborates with scholars based in Germany, Hungary and Greece. Axel Monsees's co-authors include Thomas H. Riermeier, Matthias Beller, Alexander Zapf, Uwe Dingerdissen, Franck Rataboul, Ralf Jackstell, Surendra Harkal, Armin Börner, Kathrin Junge and Christine Fischer and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and The Journal of Organic Chemistry.

In The Last Decade

Axel Monsees

43 papers receiving 1.6k citations

Peers

Axel Monsees

PCT

Mingxin Chang China

Weiping Chen China

Thomas Jerphagnon France

Yasutaka Kataoka Japan

Stefan Kaiser Switzerland

Ulrike Nettekoven Austria

Christophe Crévisy France

Olivier Baslé France

Raffaella Ferraccioli Italy

Christopher J. Cobley United Kingdom

Mingxin Chang China

Axel Monsees

821 ×0.6

787 ×0.9

340 ×0.9

196 ×0.8

102 ×1.3

PCT

Citations per year, relative to Axel Monsees Axel Monsees (= 1×) peers Mingxin Chang

Countries citing papers authored by Axel Monsees

Since Specialization

Citations

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

Fields of papers citing papers by Axel Monsees

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Axel Monsees

This figure shows the co-authorship network connecting the top 25 collaborators of Axel Monsees. A scholar is included among the top collaborators of Axel Monsees 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 Axel Monsees. Axel Monsees 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

Kadyrov, Renat & Axel Monsees. (2009). ChemInform Abstract: Practical Routes to Chiral Phospholanes. ChemInform. 40(43). 1 indexed citations

Holz, Jens, Armin Börner, Axel Monsees, & Renat Kadyrov. (2007). Chiral P-Chlorophospholane: A Versatile Building Block for the Synthesis of Ligands. Synlett. 2007(4). 599–602. 12 indexed citations

Holz, Jens, Haijun Jiao, Wolfgang Baumann, et al.. (2006). A Highly Tunable Family of Chiral Bisphospholanes for Rh‐Catalyzed Enantioselective Hydrogenation Reactions. Chemistry - A European Journal. 12(19). 5001–5013. 67 indexed citations

Hagemann, Bernhard, Kathrin Junge, Stephan Enthaler, et al.. (2005). A General Method for the Enantioselective Hydrogenation of β‐Keto Esters using Monodentate Binaphthophosphepine Ligands. Advanced Synthesis & Catalysis. 347(15). 1978–1986. 40 indexed citations

Junge, Kathrin, Bernhard Hagemann, Stephan Enthaler, et al.. (2004). Enantioselective Hydrogenation of β‐Ketoesters with Monodentate Ligands. Angewandte Chemie International Edition. 43(38). 5066–5069. 50 indexed citations

Rataboul, Franck, Alexander Zapf, Ralf Jackstell, et al.. (2004). New Ligands for a General Palladium‐Catalyzed Amination of Aryl and Heteroaryl Chlorides. Chemistry - A European Journal. 10(12). 2983–2990. 264 indexed citations

Hegedűs, Csaba, et al.. (2004). Electronic and steric effects of ligands as control elements for rhodium-catalyzed asymmetric hydroformylation. Part 3: Highly active hydroformylation of styrene. Tetrahedron Asymmetry. 15(16). 2507–2513. 15 indexed citations

Börner, Armin, et al.. (2004). Versatile Synthesis of Chiral Aminophosphine Phosphinites (AMPPs) as Ligands for Enantioselective Hydrogenation. Synthesis. 2004(12). 2047–2051. 1 indexed citations

Monsees, Axel, et al.. (2004). BINOL derived monodentate acylphosphite ligands for homogeneously catalyzed enantioselective hydrogenation. Tetrahedron Asymmetry. 15(6). 1001–1005. 26 indexed citations

10.

Streubel, Rainer, et al.. (2004). Synthesis of the first Pentacarbonyltungsten(0) Complexes with P‐Pentamethyl‐cyclopentadienyl‐substituted 1H‐Phosphirene Ligands: Crystal Structure of [{(Me₅C₅PC(H)=CPh}W(CO)₅]. Zeitschrift für anorganische und allgemeine Chemie. 630(8-9). 1215–1219. 9 indexed citations

11.

Dubrovina, Natalia V., Vitali I. Tararov, Axel Monsees, et al.. (2003). Economic preparation of 1,3-diphenyl-1,3-bis(diphenylphosphino)propane: a versatile chiral diphosphine ligand for enantioselective hydrogenations. Tetrahedron. 14(18). 2739–2745. 1 indexed citations

12.

Zapf, Alexander, Ralf Jackstell, Franck Rataboul, et al.. (2003). Practical synthesis of new and highly efficient ligands for the Suzuki reaction of aryl chlorides. Chemical Communications. 38–38. 224 indexed citations

13.

Junge, Kathrin, G. Oehme, Axel Monsees, et al.. (2003). Synthesis of new chiral monodentate aminophosphinites and their use in catalytic asymmetric hydrogenations. Journal of Organometallic Chemistry. 675(1-2). 91–96. 45 indexed citations

14.

Hegedűs, Csaba, et al.. (2003). Electronic and steric effects of ligands as control elements for rhodium-catalyzed asymmetric hydrogenation. Tetrahedron Letters. 44(50). 9025–9028. 12 indexed citations

15.

Selent, Detlef, et al.. (2003). Chiral pyrophosphites—synthesis and application as ligands in Rh(I)-catalyzed asymmetric hydrogenation. Tetrahedron Asymmetry. 14(13). 1905–1909. 16 indexed citations

16.

Monsees, Axel & Sabine Laschat. (2002). Bidentate Camphane Phosphine Phosphinites as Ligands in Asymmetric Hydrogenation of α-Dehydroamino Acids. Synlett. 2002(6). 1011–1013. 10 indexed citations

17.

Komarov, Igor V., Axel Monsees, Anke Spannenberg, et al.. (2002). Chiral Oxo- and Oxy-Functionalized Diphosphane Ligands Derived from Camphor for Rhodium(I)-Catalyzed Enantioselective Hydrogenation. European Journal of Organic Chemistry. 2003(1). 138–150. 16 indexed citations

18.

Komarov, Igor V., Axel Monsees, Renat Kadyrov, et al.. (2002). A new hydroxydiphosphine as a ligand for Rh(I)-catalyzed enantioselective hydrogenation. Tetrahedron Asymmetry. 13(15). 1615–1620. 18 indexed citations

19.

Monsees, Axel, Sabine Laschat, Marc Hotfilder, & Peter G. Jones. (1998). Diastereoselective synthesis of octahydro-14H-benzo[g]quinolino-[2,3-a]quinolidines. Improved cytotoxic activity against human brain tumor cell lines as a result of the increased rigidity of the molecular backbone. Bioorganic & Medicinal Chemistry Letters. 8(20). 2881–2884. 7 indexed citations

20.

Monsees, Axel, Sabine Laschat, Ina Dix, & Peter G. Jones. (1998). Highly Diastereoselective Alkylation of 3-Substituted Tetrahydroisoquinolines. The Journal of Organic Chemistry. 63(26). 10018–10021. 22 indexed citations

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