Inhaltspezifische Aktionen

Dr. Raffael C. Wende

Akademischer Rat, Research Associate

 

Phone and Fax:

0641 / 99 34317 (Laboratory/Office)
0641 / 99 34301 (Secretary)
0641 / 99 34309 (Fax)

 

E-Mail

 

Address:

Institute of Organic Chemistry
Justus Liebig University Giessen
Heinrich-Buff-Ring 17
35392 Giessen, Germany

Room no. B 237

Photo: Katrina Friese


Field of Work

Peptide Synthesis, Multicatalysis, Kinetic Resolution and Desymmetrization, Site-Selective Functionalization of Carbohydrates, Epoxidation and Epoxide Opening Reactions, Enantioselective Decarboxylation Reactions;

Analytik, Leitung HPLC, MS-Spektrometrie & Gaschromatographie

  

Publications

 

Capture and Reactivity of an Elusive Carbon–Sulfur Centered Biradical. D. Gerbig, B. Bernhardt, R. C. Wende, P. R. Schreiner, J. Phys. Chem, A 2020, 124, 2014-2018.

 

In Situ Switching of Site-Selectivity with Light in the Acetylation of Sugars with Azopeptide Catalysts. D. Niedek, F. R. Erb, C. Topp, A. Seitz, R. C. Wende, A. K. Eckhardt, J. Kind, D. Herold, C. M. Thiele, P. R. Schreiner, J. Org. Chem. 2020, 85, 1835-1846.

 

TEMPO-functionalized mesoporous silica particles as heterogeneous oxidation catalysts in flow. J. S. Schulze, J. Migenda, M. Becker, S. M. M. Schuler, R. C. Wende, P. R. Schreiner, B. M. Smarsly, J. Mat. Chem. A 2020, 8, 4107-4117.

 

1,3-Dioxolane-4-ol Hemiacetal Stores Formaldehyde and Glycolaldehyde in the Gas-Phase. A. K. Eckhardt, R. C. Wende, P. R. Schreiner, J. Am. Chem. Soc. 2018, 140, 12333-12336.

 

Total Synthesis and Structural Revision of the Antibiotic Tetrapeptide GE81112A. G. Jürjens, S. M. M. Schuler, M. Kurz, S. Petit, C. Couturier, F. Jeannot, F. Nguyen, R. C. Wende, P. E. Hammann, D. N. Wilson, E. Bacqué, C. Pöverlein, A. Bauer, Angew. Chem. Int. Ed. 2018, 57, 12157-12161.

 

Gas-phase sugar formation using hydroxymethylene as the reactive formaldehyde isomer. A. K. Eckhardt, M. M. Linden, R. C. Wende, B. Bernhardt, and P. R. Schreiner, Nature Chem. 2018, 10, 1141-1147.

 

London dispersion as important factor for the stabilization of (Z)-azobenzenes in the presence of hydrogen bonding. A. H. Heindl, R. C. Wende, H. A. Wegner, Beilstein J. Org. Chem. 2018, 14, 1238-1243.

 

Synthesis of Enantioenriched Phthalide and Isoindolinone Derivatives from 2-Formylbenzoic Acid. D. Niedek, S. M. M. Schuler, C. Eschmann, R. C. Wende, A. Seitz, F. Keul, P. R. Schreiner, Synthesis 2017, 49, 371-382.

 

Chiral Building Blocks Based on 1,2-Disubstituted Diamantanes. A. A. Fokin, A. E. Pashenko, V. V. Bakhonsky, T. S. Zhuk, L. V. Chernish, P. A. Gunchenko, A. O. Kushko, J. Becker, R. C. Wende, P. R. Schreiner, Synthesis 2017, 49, 2003-2008.

 

Uncovering Key Structural Features of an Enantioselective Peptide-Catalyzed Acylation Utilizing Advanced NMR Techniques. E. Procházková, A. Kolmer, J. Ilgen, M. Schwab, L. Kaltschnee, M. Fredersdorf, V. Schmidts, R. C. Wende, P. R. Schreiner, C. M. Thiele, Angew. Chem. Int. Ed. 2016, 55, 15754-15759.

 

The Enantioselective Dakin–West Reaction. R. C. Wende, A. Seitz, D. Niedek, S. M. M. Schuler, C. Hofmann, J. Becker, P. R. Schreiner, Angew. Chem. Int. Ed. 2016, 55, 2719-2723.

 

Functionality, Effectiveness, and Mechanistic Evaluation of a Multicatalyst-Promoted Reaction Sequence by Electrospray Ionization Mass Spectrometry. M. W. Alachraf, R. C. Wende, S. M. M. Schuler, P. R. Schreiner, W. Schrader, Chem.–Eur. J. 2015, 21, 16203-16208.

 

En route to multicatalysis: kinetic resolution of trans-cycloalkane-1,2-diols via oxidative esterification. C. Hofmann, S. M. M. Schuler, R. C. Wende, P. R. Schreiner, Chem. Commun. 2014, 50, 1221-1223.

 

Lipophilic Oligopeptides for Chemo- and Enantioselective Acyl Transfer Reactions onto Alcohols. C. E. Müller, D. Zell, R. Hrdina, R. C. Wende, L. Wanka, S. M. M. Schuler, P. R. Schreiner, J. Org. Chem. 2013, 78, 8465-8484.

 

Evolution of asymmetric organocatalysis: multi- and retrocatalysis. R. C. Wende, P. R. Schreiner, Green Chem. 2012, 14, 1821-1849.

 

Enantiomerically enriched trans-diols from alkenes in one pot: a multicatalyst approach. R. Hrdina, C. E. Müller, R. C. Wende, L. Wanka, P. R. Schreiner, Chem. Commun. 2012, 48, 2498-2500.

 

A Multicatalyst System for the One-Pot Desymmetrization/Oxidation of meso-1,2-Alkane Diols. C. E. Müller, R. Hrdina, R. C. Wende, P. R. Schreiner, Chem.–Eur. J. 2011, 17, 6309-6314.

 

Silicon−(Thio)urea Lewis Acid Catalysis. R. Hrdina, C. E. Müller, R. C. Wende, K. M. Lippert, M. Benassi, B. Spengler, P. R. Schreiner, J. Am. Chem. Soc. 2011, 133, 7624-7627.

 

Isolation of the key intermediates in the catalyst-free conversion of oxiranes to thiiranes in water at ambient temperature. C. M. Kleiner, L. Horst, C. Würtele, R. Wende, P. R. Schreiner, Org. Biomol. Chem. 2009, 7, 1397-1403.