2012/05/16
 
 
SFB 749
ERC: European Research Council
 
German Academy of Sciences Leopoldina Bavarian Academy of Science Academie des sciences (Paris)
 
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Group of Prof. Dr. Paul Knochel | Department Chemie | Ludwig-Maximilians-Universität

 

 

News

  

  • Das Script zur OCIV-Vorlesung 2012 kann nun heruntergeladen werden.
     
  • The Gold Nagoya Medal of Organic Chemistry 2012 has been awarded to Paul Knochel.
    The Gold Medal is awarded every year to an organic chemist who has made significant original contributions to the field in its broadest sense.
     
  • Paul Knochel is the Winner of the 2011 EROS (Encyclopedia of Reagents for Organic Synthesis) Best Reagent Award.
     
  • The "Gesellschaft Deutscher Chemiker (GDCh)" has awarded the "Karl-Ziegler-Preis 2009" to Paul Knochel for his research work between the fields of organometallic chemistry, organic chemistry and catalysis.
     
  • Paul Knochel received an Advanced Investigator Grant (2.000.000 €)  for research on "new metalorganic compounds" from the European Research Council (ERC). 
  • Paul Knochel is elected to be a Member of the Bavarian Academy of Science 2008
  • Paul Knochel is elected to be a Member of the Académie des sciences (Paris) 2007
     
  • The "Eli Lilly and Company" has awarded the "Lilly European Distinguished Lectureship Award 2007" to Paul Knochel for his research work on Organic Synthesis.

 

 

 

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Recent Publications

 

 

Preparation of Solid Salt-Stabilized Functionalized Organozinc Compounds and their Application to Cross-Coupling and Carbonyl Addition Reactions.gif
  • Bernhardt, Sebastian; Manolikakes, Georg; Kunz, Thomas; Knochel, Paul. Preparation of Solid Salt-Stabilized Functionalized Organozinc Compounds and their Application to Cross-Coupling and Carbonyl Addition Reactions. Angew. Chem. Int. Ed. 2011, 50, 9205–9209.
 
Regio- and Chemoselective Metalation of Arenes and Heteroarenes Using Hindered Metal Amide Bases.gif
  • Haag, Benjamin; Mosrin, Marc; Ila, Hiriyakkanavar; Malakhov, Vladimir; Knochel, Paul. Regio- and Chemoselective Metalation of Arenes and Heteroarenes Using Hindered Metal Amide Bases. Angew. Chem. Int. Ed. 2011, 50, 9794–9824.

 

 
Highly Diastereoselective Arylations of Substituted Piperidines.gif
  • Seel, Stephanie; Thaler, Tobias; Takatsu, Keishi; Zhang, Cong; Zipse, Hendrik; Straub, Bernd F.; Mayer, Peter; Knochel, Paul. Highly Diastereoselective Arylations of Substituted Piperidines. J. Am. Chem. Soc. 2011, 133, 4774–4777.
 
Lewis Acid Promoted Benzylic Cross-Couplings of Pyridines with Aryl Bromides.gif
  • Duez, Stéphanie; Steib, Andreas K.; Manolikakes, Sophia M.; Knochel, Paul. Lewis Acid Promoted Benzylic Cross-Couplings of Pyridines with Aryl Bromides. Angew. Chem. Int. Ed. 2011, 50, 7686–7690.
 
One-Pot Preparation of Magnesium Di(hetero)aryl- and Magnesium Dialkenylboronates for Suzuki–Miyaura Cross-Coupling Reactions.gif
  • Haag, Benjamin A.; Sämann, Christoph; Jana, Anukul; Knochel, Paul. Practical One-Pot Preparation of Magnesium Di(hetero)aryl- and Magnesium Dialkenylboronates for Suzuki–Miyaura Cross-Coupling Reactions. Angew. Chem. Int. Ed. 2011, 50, 7290–7294.
 
Highly Diastereoselective Iron-Mediated C(sp2)–C(sp3) Cross-Coupling Reactions between Aryl Grignard Reagents and Cyclic Iodohydrine Derivatives..gif
  • Steib, Andreas K.; Thaler, Tobias; Komeyama, Kimihiro; Mayer, Peter; Knochel, Paul. Highly Diastereoselective Iron-Mediated C(sp2)–C(sp3) Cross-Coupling Reactions between Aryl Grignard Reagents and Cyclic Iodohydrine Derivatives. Angew. Chem. Int. Ed. 2011, 50, 3303–3307.
 
Regioselective Functionalization of the Thiazole Scaffold Using TMPMgCl•LiCl and TMP2Zn•2MgCl2•2LiCl..gif
  • Dunst, Cora, Knochel, Paul. Regioselective Functionalization of the Thiazole Scaffold Using TMPMgCl•LiCl and TMP2Zn•2MgCl2•2LiCl. J. Org. Chem., 2011, 76, 6972–6978.
 
Selective Magnesiation or Zincation of Highly Functionalized Alkenes and Cycloalkenes Using 2,2,6,6-Tetramethylpiperidyl Bases.gif
  • Bresser, Tomke; Knochel, Paul. Selective Magnesiation or Zincation of Highly Functionalized Alkenes and Cycloalkenes Using 2,2,6,6-Tetramethylpiperidyl Bases. Angew. Chem. Int. Ed. 2011, 50, 1914–1917.
 
Selective Multiple Magnesiations of the Thieno[3,2-b]thiophene Scaffold.gif
  • Kunz, Thomas; Knochel, Paul. Selective Multiple Magnesiations of the Thieno[3,2-b]thiophene Scaffold. Chem. Eur. J., 2011, 17, 866–872.
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