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Dr. Jörg Pabel

Department Pharmazie
- Zentrum für Pharmaforschung -
Ludwig-Maximilians-Universität München
Butenandtstraße 7
D-81377 München

Zi.Nr.: C1.061
Tel.: +49 (0)89 2180 77244
Fax.: +49 (0)89 2180 77247





Dissertation

Asymmetrische Synthese von Antagonisten der Polyamin-Bindungsstelle des NMDA-Rezeptors

Publications

J. Pabel, E. Wadenstorfer, K.T. Wanner, "Asymmetric Synthesis of Pyridol[1,2-c]pyrimidones, Zeitschrift für Naturforschung B, 2009 (64b), 6, 653–661. (Link)

C.-J. Koch, S. Šimonyiová, J. Pabel, A. Kärtner, K. Polborn, K. T. Wanner, “Asymmetric Synthesis with 6-tert-Butyl-5-methoxy-6-methyl-3,6-dihydro-2H-1,4-oxazin-2-one as a New Chiral Glycine Equivalent: Preparation of Enantiomerically Pure α-Tertiary and α-Quaternary α-Amino Acids”, Eur. J. Org. Chem., 2003,1244-1263. (DOI)

C. E. Hoesl, M. Maurus, J. Pabel, K. Polborn, K. T. Wanner, “Generation of chiral N-acylpyridinium ions by means of silyl triflates and their diastereoselective trapping reaction: Formation of N-acyldihydropyridines and N-acyldihydropyridones”, Tetrahedron, 2002, 58, 6757-6770.

C. E. Hoesl, J. Pabel, K. Polborn, K. T. Wanner, „Synthesis of Sterically Demanding 3-Silylpyridines and their Use in Asymmetric Synthesis with Chiral N-Acyliminium Ions“, Heterocycles, 2002, 58, 383-392.

J. Pabel, G. Höfner, K. T. Wanner, "Synthesis and Resolution of Racemic Eliprodil and Evaluation of the Enantiomers of Eliprodil as NMDA Receptor Antagonists", Bioorg. Med. Chem. Lett.,2000, 10, 1377-1380.

J. Pabel, C. E. Hösl, M. Maurus, M. Ege, K. T. Wanner, "Generation of N-Acylpyridinium Ions from Pivaloyl Chloride and Pyridine Derivatives by Means of Silyl Triflates", J. Org. Chem., 2000, 65, 9272-9275.

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