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Peer-reviewed articles

23.

S. Quintero Duque, I. Fleischer,* Synthesis 2017, accepted. “Tandem and One-Pot Hydroformylation Reactions of Acrylates”  DOI: 10.1055/s-0036-1588394

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22.

V. Hirschbeck, P. H. Gehrtz, I. Fleischer,* J. Am. Chem. Soc2016, 138, 16794.   published onlineRegioselective thiocarbonylation of vinyl arenes“ DOI: 10.1021/jacs.6b11020 

21.

I. Fleischer,* Angew. Chem. Int. Ed2016, 55, 8486. „Structures, reactions, and mechanisms: stereochemistry in the broadest sense at the 51st Bürgenstock Conference“ DOI: 10.1002/anie.201605274
20.

I. Fleischer,* Angew. Chem. Int. Ed. 2016, 55, 7582. „Chiral catalyst design: cyclopentadiene-based Brønsted acids“ DOI: 10.1002/anie.201603672

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19.

P. H. Gehrtz, V. Hirschbeck, B. Ciszek, I. Fleischer,* Synthesis  2016, 48, 1573. „Carbonylations of alkenes in the total synthesis of natural compounds“ DOI: 10.1055/s-0035-1562550

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 *created with tagul

18.

C. Kubis, I. Profir, I. Fleischer, W. Baumann, D. Selent, C. Fischer, A. Spannenberg, R. Ludwig, D. Hess, R. Franke, A. Börner, Chem. Eur. J. 2016, 22, 2746. „In Situ FTIR and NMR Spectroscopic Investigations on Ruthenium-Based Catalysts for Alkene Hydroformylation“ DOI: 10.1002/chem.201504051    
17. S. Fritschi, W. Korth, J. Julis, D. Kruse, H. Hahn, R. Franke, I. Fleischer, A. D. Chowdhury, N. Weding, R. Jackstell, M. Beller, A. Jess, Chem. Ing. Tech. 2015, 87, 1313. „Synthesis of Aliphatic Aldehydes from Alkanes and Carbon Dioxide: Valeraldehyde from Butane and CO2 – Feasibility and Limitations“ DOI: 10.1002/cite.201400158

16. 

 P. H. Gehrtz, V. Hirschbeck, I. Fleischer,* Chem. Commun. 2015, 51, 12574. „A recyclable CO surrogate in regioselective alkoxycarbonylation of alkenes: indirect use of carbon dioxide“ DOI: 10.1039/C5CC05012J.

15. 

 F. Bächle, I. Fleischer, A. Pfaltz, Adv. Synth. Catal. 2015,  357, 2247. „Mass spectrometric screening of racemic amine catalysts for enantioselective Michael additions“ (VIP paper) DOI: 10.1002/adsc.201500224

14.

 S. Quintero Duque, K. M. Driller, I. Fleischer,* Tetrahedron Lett.  2015, 56, 2634. „Metal-catalyzed carbonylation of alkynes: key aspects and recent development“ (Invited Digest paper) DOI: 10.1016/j.tetlet.2015.04.943

 

13.

I. Fleischer,* J. Pospech, RSC Advances 20155, 493. "Brønsted acid-catalyzed hydroarylation of activated olefins"  DOI: 10.1039/C4RA13647K

12.

 L. Wu, I. Fleischer, M. Zhang, Q. Liu, R. Franke, R. Jackstell, M. Beller, ChemSusChem 20147, 3260."Using aqueous ammonia in hydroaminomethylation reactions: ruthenium-catalyzed synthesis of tertiary amines"

11.

I. Profir, M. Beller,* I. Fleischer,* Org. Biomol. Chem. 201412, 6972. "Novel ruthenium-catalyst for hydroesterification of olefins with formatesDOI: 10.1039/C4OB01246A 

10.

Q. Liu, L. Wu, I. Fleischer,* D. Selent, R. Franke, R. Jackstell, M. Beller,* Chem. Eur. J. 201420, 6888. „Development of a ruthenium/phosphite catalyst system for domino-hydroformylation-reduction of olefins with carbon dioxide
9.

L. Wu, Q. Liu, I. Fleischer, R. Jackstell, M. Beller, Nature Commun20145, 3091. „Ruthenium-catalyzed alkoxycarbonylation of alkenes with carbon dioxide"

8.

L. Wu, I. Fleischer, R. Jackstell, I. Profir, R. Franke, M. Beller, J. Am. Chem. Soc. 2013135, 14306. Ruthenium-catalyzed hydroformylation/reduction of olefins to alcohols: extending the scope to internal alkenes”

7.

L. Wu, I. Fleischer, R. Jackstell, M. Beller, J. Am. Chem. Soc2013135, 3989. Efficient and regioselective ruthenium-catalyzed hydroaminomethylation of olefins

6.

I. Fleischer, L. Wu, I. Profir, R. Jackstell, R. Franke, M. Beller, Chem. Eur. J. 201319, 10589.Towards the development of a selective ruthenium-catalyzed hydroformylation of olefins”

5.

I. Fleischer, R. Jennerjahn, D. Cozzula, R. Franke, R. Jackstell, M. Beller, ChemSusChem 20136, 417. „A unique palladium catalyst for efficient and selective alkoxycarbonylation of olefins with formates

4.

J. Pospech, I. Fleischer, R. Franke, S. Buchholz, M. Beller, Angew. Chem. Int. Ed. 201352, 2852. „Alternative metals in homogenous hydroformylation reactions

3.

I. Fleischer, K. Dyballa, R. Jennerjahn, R. Jackstell, R. Franke, A. Spannenberg, M. Beller, Angew. Chem. Int. Ed. 201352, 2949. „From olefins to alcohols: efficient and regioselective ruthenium-catalyzed domino-hydroformylation-reduction-sequence

2.

I. Fleischer, A. Pfaltz, Chem. Eur. J. 201016, 95. Enantioselective Michael addition to α,β-unsaturated aldehydes: Combinatorial catalyst preparation and screening, reaction optimization and mechanistic studies” (highlighted in Nachrichten in Chemie 2010/2;Synfacts 2010, 236.)

1. 

 I. Fleischer, Š. Toma, Collect. Czech. Chem. Commun200469, 330. Synthesis of new chiral 1,2-disubstituted ferrocenes

 

  Patents

8.

R. Franke, K. M. Dyballa, M. Beller, R. Jackstell, Q. Liu, M. Zhang, L. Wu, I. Fleischer, EP 2975019, 2016. „Ruthenium catalyzed hydroaminomethylation of alkenes    

7.

R. Franke, J. Julis, D. Fridag, K. M. Dyballa, N. Weding, A. D. Chowdhury, M. Beller, R. Jackstell, I. Fleischer, B. Percia, EP2910546A1, 2015. „Method for the photocatalytic acceptor-free dehydrogenation of hydrocarbazoles and hydroindoles“    

6.

R. Franke, J. Julis, D. Fridag, K. M. Dyballa, N. Weding, A. D. Chowdhury, M. Beller, R. Jackstell, I. Fleischer, B. Percia, EP2910541A1, 2015. „Method for photocatalytic acceptor-free dehydrogenation of alkanes and alcohols“    

5.

L. Wu, M. Beller, R. Jackstell, Q. Liu, I. Fleischer, WO 2015018845, 2015. „Method for the synthesis of saturated carboxylic acid esters    

4. 

R. Franke, K. M. Dyballa, D. Hess, B. Hamers, D. Fridag, M. Beller, I. Fleischer, R. Jackstell, I. Profir, L. Wu, WO 2014118046, 2014. „Method for the carbonylation of olefins

3.

R. Franke, K. M. Dyballa, D. Hess, B. Hamers, D. Fridag, M. Beller, R. Jackstell, I. Fleischer, L. Wu, WO 2014118042, 2014. „Method for the selective ruthenium-catalyzed hydroaminomethylation of olefins"

2.

R. Franke, K. M. Dyballa, D. Hess, B. Hamers, D. Fridag, M. Beller, R. Jackstell, I. Fleischer, L. Wu, WO 2014118038, 2014. „Phosphorus ligands and method for the selective ruthenium-catalyzed hydroaminomethylation of olefins“  

1.

R. Franke, D. Hess, M. Beller, R. Jackstell, D. Cozzula, I. Fleischer, R. Jennerjahn, WO 2013092478,2013. „Process for preparing esters from formates and olefinically unsaturated compounds

Book Chapters

1.

I. Fleischer, E. Mejia, in Science of Synthesis Reference Library: C–1 Building Blocks in Organic Synthesis (Ed. P. W. N. M. van Leeuwen), Thieme Verlag, Stuttgart, 2013. „Tandem hydroformylation of alkenes    

Miscellaneous

3. I. Fleischer, SYNFORM 2015, A49. “Young Career Focus    
2.  I. Fleischer, J. Teichert, Nachr. Chem. 2014, 62, 904. „17. Steinheimer Gespräche    
1.

C. Bryan, V. Aurregi, M. Lautens, A. Pfaltz, I. Fleischer, Org. Synth. 2009, 86, 36.                            2-(2,2-Dibromoethenyl)-benzenamine    

  1. Fakulty of Chemistry and Pharmacy
  2. Institute of Organic Chemistry

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Ivana Fleischer

 

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