Year |
Citation |
Score |
2023 |
Oechsner RM, Lindenmaier IH, Fleischer I. Nickel Catalyzed Cross-Coupling of Aryl and Alkenyl Triflates with Alkyl Thiols. Organic Letters. 25: 1655-1660. PMID 36877862 DOI: 10.1021/acs.orglett.3c00218 |
0.329 |
|
2020 |
Kathe PM, Caciuleanu A, Berkefeld A, Fleischer I. Tandem Olefin Isomerization/Cyclization Catalyzed by Complex Nickel Hydride and Brønsted Acid. The Journal of Organic Chemistry. PMID 33174749 DOI: 10.1021/acs.joc.0c02033 |
0.403 |
|
2020 |
Kathe P, Fleischer I. Light expands a catalyst's repertoire. Science (New York, N.Y.). 368: 242-243. PMID 32299937 DOI: 10.1126/Science.Abb2104 |
0.433 |
|
2020 |
Schmidt TA, Ciszek B, Kathe P, Fleischer I. Tandem Acid/Pd-Catalyzed Reductive Rearrangement of Glycol Derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 26: 3641-3646. PMID 31951298 DOI: 10.1002/Chem.202000251 |
0.408 |
|
2019 |
Hirschbeck V, Böldl M, Gehrtz PH, Fleischer I. Tandem Acyl Substitution/Michael Addition of Thioesters with Vinylmagnesium Bromide. Organic Letters. 21: 2578-2582. PMID 30933515 DOI: 10.1021/Acs.Orglett.9B00538 |
0.415 |
|
2019 |
Kathe PM, Fleischer I. Palladium-Catalyzed Tandem Isomerization/Hydrothiolation of Allylarenes. Organic Letters. 21: 2213-2217. PMID 30868888 DOI: 10.1021/Acs.Orglett.9B00504 |
0.593 |
|
2019 |
Gehrtz PH, Geiger V, Schmidt T, Sršan L, Fleischer I. Cross-Coupling of Chloro(hetero)arenes with Thiolates Employing a Ni(0)-Precatalyst. Organic Letters. 21: 50-55. PMID 30557032 DOI: 10.1021/Acs.Orglett.8B03476 |
0.464 |
|
2019 |
Böldl M, Fleischer I. Front Cover: Dehydrative Coupling of Benzylic Alcohols Catalyzed by Brønsted Acid/Lewis Base (Eur. J. Org. Chem. 34/2019) European Journal of Organic Chemistry. 2019: 5828-5828. DOI: 10.1002/Ejoc.201901233 |
0.359 |
|
2019 |
Böldl M, Fleischer I. Dehydrative Coupling of Benzylic Alcohols Catalyzed by Brønsted Acid/Lewis Base European Journal of Organic Chemistry. 2019: 5856-5861. DOI: 10.1002/Ejoc.201900965 |
0.358 |
|
2019 |
Kathe P, Fleischer I. Cooperative Use of Brønsted Acids and Metal Catalysts in Tandem Isomerization Reactions of Olefins Chemcatchem. 11: 3343-3354. DOI: 10.1002/Cctc.201900830 |
0.521 |
|
2018 |
Gehrtz PH, Kathe P, Fleischer I. Nickel-Catalyzed Coupling of Arylzinc Halides with Thioesters. Chemistry (Weinheim An Der Bergstrasse, Germany). 24: 8774-8778. PMID 29750383 DOI: 10.1002/Chem.201801887 |
0.434 |
|
2018 |
Ciszek B, Fleischer I. Homogeneous Palladium-Catalyzed Transfer Hydrogenolysis of Benzylic Alcohols Using Formic Acid as Reductant. Chemistry (Weinheim An Der Bergstrasse, Germany). 24: 12259-12263. PMID 29644726 DOI: 10.1002/Chem.201801466 |
0.578 |
|
2018 |
Hirschbeck V, Fleischer I. Synthesis of Benzofuranones via Palladium-Catalyzed Intramolecular Alkoxycarbonylation of Alkenylphenols. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29323440 DOI: 10.1002/Chem.201705808 |
0.492 |
|
2018 |
Hirschbeck V, Gehrtz PH, Fleischer I. Metal-Catalyzed Synthesis and Use of Thioesters: Recent Developments. Chemistry (Weinheim An Der Bergstrasse, Germany). 24: 7092-7107. PMID 29178255 DOI: 10.1002/Chem.201705025 |
0.434 |
|
2018 |
Hirschbeck V, Gehrtz PH, Fleischer I. Frontispiece: Metal-Catalyzed Synthesis and Use of Thioesters: Recent Developments Chemistry - a European Journal. 24. DOI: 10.1002/Chem.201882863 |
0.355 |
|
2017 |
Fleischer I, Quintero-Duque S. Tandem and One-Pot Hydroformylation/Michael Reactions of Acrylates Synthesis. 49: 925-932. DOI: 10.1055/S-0036-1588394 |
0.435 |
|
2016 |
Hirschbeck V, Gehrtz PH, Fleischer I. Regioselective Thiocarbonylation of Vinyl Arenes. Journal of the American Chemical Society. 138: 16794-16799. PMID 27966917 DOI: 10.1021/Jacs.6B11020 |
0.513 |
|
2016 |
Fleischer I. Chiral Catalyst Design: Cyclopentadiene-Based Brønsted Acids. Angewandte Chemie (International Ed. in English). 55: 7582-4. PMID 27219010 DOI: 10.1002/Anie.201603672 |
0.512 |
|
2016 |
Kubis C, Profir I, Fleischer I, Baumann W, Selent D, Fischer C, Spannenberg A, Ludwig R, Hess D, Franke R, Börner A. In Situ FTIR and NMR Spectroscopic Investigations on Ruthenium-Based Catalysts for Alkene Hydroformylation. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 2746-57. PMID 26785230 DOI: 10.1002/Chem.201504051 |
0.468 |
|
2016 |
Fleischer I, Gehrtz P, Hirschbeck V, Ciszek B. Carbonylations of Alkenes in the Total Synthesis of Natural Compounds Synthesis. 48: 1573-1596. DOI: 10.1055/S-0035-1560431 |
0.416 |
|
2016 |
Fleischer I. ChemInform Abstract: Chiral Catalyst Design: Cyclopentadiene-Based Broensted Acids Cheminform. 47. DOI: 10.1002/CHIN.201636210 |
0.385 |
|
2015 |
Gehrtz PH, Hirschbeck V, Fleischer I. A recyclable CO surrogate in regioselective alkoxycarbonylation of alkenes: indirect use of carbon dioxide. Chemical Communications (Cambridge, England). 51: 12574-7. PMID 26152898 DOI: 10.1039/C5Cc05012J |
0.396 |
|
2015 |
Fleischer I, Pospech J. Brønsted acid-catalyzed hydroarylation of activated olefins Rsc Advances. 5: 493-496. DOI: 10.1039/C4Ra13647K |
0.359 |
|
2015 |
Quintero-Duque S, Dyballa KM, Fleischer I. Metal-catalyzed carbonylation of alkynes: key aspects and recent development Tetrahedron Letters. 56: 2634-2650. DOI: 10.1016/J.Tetlet.2015.04.043 |
0.462 |
|
2015 |
Fritschi S, Korth W, Julis J, Kruse D, Hahn H, Franke R, Fleischer I, Chowdhury AD, Weding N, Jackstell R, Beller M, Jess A. Synthesis of Aliphatic Aldehydes from Alkanes and Carbon Dioxide: Valeraldehyde from Butane and CO2 - Feasibility and Limitations Chemie-Ingenieur-Technik. 87: 1313-1326. DOI: 10.1002/Cite.201400158 |
0.487 |
|
2015 |
Bächle F, Fleischer I, Pfaltz A. Mass Spectrometric Screening of Racemic Amine Catalysts for Enantioselective Michael Additions Advanced Synthesis and Catalysis. 357: 2247-2254. DOI: 10.1002/Adsc.201500224 |
0.65 |
|
2014 |
Wu L, Fleischer I, Zhang M, Liu Q, Franke R, Jackstell R, Beller M. Using aqueous ammonia in hydroaminomethylation reactions: ruthenium-catalyzed synthesis of tertiary amines. Chemsuschem. 7: 3260-3. PMID 25223274 DOI: 10.1002/Cssc.201402626 |
0.617 |
|
2014 |
Profir I, Beller M, Fleischer I. Novel ruthenium-catalyst for hydroesterification of olefins with formates. Organic & Biomolecular Chemistry. 12: 6972-6. PMID 25098865 DOI: 10.1039/C4Ob01246A |
0.592 |
|
2014 |
Liu Q, Wu L, Fleischer I, Selent D, Franke R, Jackstell R, Beller M. Development of a ruthenium/phosphite catalyst system for domino hydroformylation-reduction of olefins with carbon dioxide. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 6888-94. PMID 24811949 DOI: 10.1002/Chem.201400358 |
0.646 |
|
2014 |
Wu L, Liu Q, Fleischer I, Jackstell R, Beller M. Ruthenium-catalysed alkoxycarbonylation of alkenes with carbon dioxide. Nature Communications. 5: 3091. PMID 24518431 DOI: 10.1038/Ncomms4091 |
0.478 |
|
2014 |
Profir I, Beller M, Fleischer I. Novel ruthenium-catalyst for hydroesterification of olefins with formates Organic and Biomolecular Chemistry. 12: 6972-6976. DOI: 10.1039/c4ob01246a |
0.552 |
|
2014 |
Liu Q, Wu L, Fleischer I, Selent D, Franke R, Jackstell R, Beller M. Cover Picture: Development of a Ruthenium/Phosphite Catalyst System for Domino Hydroformylation-Reduction of Olefins with Carbon Dioxide (Chem. Eur. J. 23/2014) Chemistry - a European Journal. 20: 6805-6805. DOI: 10.1002/Chem.201490091 |
0.572 |
|
2014 |
Liu Q, Wu L, Fleischer I, Selent D, Franke R, Jackstell R, Beller M. Development of a ruthenium/Phosphite catalyst system for domino hydroformylation-reduction of olefins with carbon dioxide Chemistry - a European Journal. 20: 6888-6894. DOI: 10.1002/chem.201400358 |
0.527 |
|
2013 |
Wu L, Fleischer I, Jackstell R, Profir I, Franke R, Beller M. Ruthenium-catalyzed hydroformylation/reduction of olefins to alcohols: extending the scope to internal alkenes. Journal of the American Chemical Society. 135: 14306-12. PMID 23987582 DOI: 10.1021/Ja4060977 |
0.493 |
|
2013 |
Fleischer I, Wu L, Profir I, Jackstell R, Franke R, Beller M. Towards the development of a selective ruthenium-catalyzed hydroformylation of olefins. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 10589-94. PMID 23828402 DOI: 10.1002/Chem.201300899 |
0.625 |
|
2013 |
Pospech J, Fleischer I, Franke R, Buchholz S, Beller M. Alternative metals for homogeneous catalyzed hydroformylation reactions. Angewandte Chemie (International Ed. in English). 52: 2852-72. PMID 23436281 DOI: 10.1002/Anie.201208330 |
0.574 |
|
2013 |
Wu L, Fleischer I, Jackstell R, Beller M. Efficient and regioselective ruthenium-catalyzed hydro-aminomethylation of olefins. Journal of the American Chemical Society. 135: 3989-96. PMID 23419202 DOI: 10.1021/Ja312271C |
0.605 |
|
2013 |
Fleischer I, Dyballa KM, Jennerjahn R, Jackstell R, Franke R, Spannenberg A, Beller M. From olefins to alcohols: efficient and regioselective ruthenium-catalyzed domino hydroformylation/reduction sequence. Angewandte Chemie (International Ed. in English). 52: 2949-53. PMID 23404711 DOI: 10.1002/Anie.201207133 |
0.473 |
|
2013 |
Fleischer I, Jennerjahn R, Cozzula D, Jackstell R, Franke R, Beller M. A unique palladium catalyst for efficient and selective alkoxycarbonylation of olefins with formates. Chemsuschem. 6: 417-20. PMID 23322709 DOI: 10.1002/Cssc.201200759 |
0.642 |
|
2013 |
Wu L, Fleischer I, Jackstell R, Profir I, Franke R, Beller M. Ruthenium-catalyzed hydroformylation/reduction of olefins to alcohols: Extending the scope to internal alkenes Journal of the American Chemical Society. 135: 14306-14312. DOI: 10.1021/ja4060977 |
0.415 |
|
2013 |
Pospech J, Fleischer I, Franke R, Buchholz S, Beller M. Alternative Metalle für die homogen katalysierte Hydroformylierung Angewandte Chemie. 125: 2922-2944. DOI: 10.1002/Ange.201208330 |
0.381 |
|
2010 |
Fleischer I, Pfaltz A. Enantioselective Michael addition to alpha,beta-unsaturated aldehydes: combinatorial catalyst preparation and screening, reaction optimization, and mechanistic studies. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 95-9. PMID 19918823 DOI: 10.1002/Chem.200902449 |
0.64 |
|
2010 |
Fleischer I, Pfaltz A. Enantioselective michael addition to α,β-Unsaturated aldehydes: Combinatorial catalyst preparation and screening, reaction optimization and mechanistic studies Chemistry - a European Journal. 16: 95-99. DOI: 10.1002/chem.200902449 |
0.572 |
|
2004 |
Fleischer I, Toma Š. Synthesis of New Chiral 1,2-Disubstituted Ferrocenes Collection of Czechoslovak Chemical Communications. 69: 330-338. DOI: 10.1135/Cccc20040330 |
0.315 |
|
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