LMU Header LMU M;uuml;nchen CUP Wiki
Suche:
CUP  |  EDV-Service/Webmail  |  Intranet  |  Sitemap  |  LMU-Portal
 


Dr. Lars Allmendinger

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

Zi.Nr.: C1.063
Tel.: +49 (0)89 2180 77803
Fax.: +49 (0)89 2180 77247
Mail: Lars.Allmendinger@cup.uni-muenchen.de




Aufgabenbereiche

Analytik
Lehre


Dissertation

Studien zur Totalsynthese des Antibiotikums Tetrodecamycin



Mitgliedschaften

Deutsche Pharmazeutische Gesellschaft

Gesellschaft Deutscher Chemiker, Fachgruppe Magnetische Resonanzspektroskopie



Publikationen

18. T. Wein, M. Petrera, L. Allmendinger, G. Höfner, J. Pabel, K. T. Wanner, "Different Binding Modes of Small and Large Binders of GAT1" ChemMedChem 2016, 11, 509–518. (DOI)

17. M. Petrera, T. Wein, L. Allmendinger, M. Sindelar, J. Pabel, G. Höfner, K. T. Wanner, "Development of Highly Potent GAT1 Inhibitors: Synthesis of Nipecotic Acid Derivatives by Suzuki-Miyaura Cross-Coupling Reactions” ChemMedChem 2016, 11, 519–538. (DOI)


16. L. Allmendinger, K. T. Wanner, ”Synthesis of [2H7]indatraline” J. Label Compd. Radiopharm 2014, 57, 721-724. (DOI)



15. S. H. Grimm, L. Allmendinger, G. Höfner, K. T. Wanner, "Enantiopurity Determination of the Enantiomers of the Triple Reuptake Inhibitor Indatraline” Chirality, 2013, 25, 923-933. (DOI)



14. I. Sitka, L. Allmendinger, G. Fülep, G. Höfner, K. T. Wanner, "Synthesis of N-substituted acyclic β-amino acids and their investigation as GABA uptake inhibitors" Eur. J. Med. Chem., 2013, 65, 487-499. (DOI)



13. J. Pabel, M. Faust, C. Prehn, B. Wörlein, L. Allmendinger, G. Höfner, K. T. Wanner, "Development of a (S)-1-{2-[tris(4-methoxyphenyl)methoxy]ethyl}piperidine-3-carboxylic acid [(S)-SNAP-5114] carba analogue inhibitor for murine y-aminobutyric acid transporter type 4" ChemMedChem, 2012, 7, 1245 – 1255. (DOI)

12. C. D. Mayer, L. Allmendinger, F. Bracher, "Synthesis of novel steroid analogues containing nitrile and disulfide moieties via palladium-catalyzed cross-coupling reactions" Tetrahedron, 2012, 6, 1810-1818. (DOI)



11. I. Wetzel, L. Allmendinger, F. Bracher, "Revised Structure of the Alkaloid Drymaritin" J. Nat. Prod., 2009, 72, 1908-1910. (DOI)



10. J. H. Spatz, S. J. Welsch, D.-E. Duhaut, N. Jaeger, T. Boursier, M. Fredrich, L. Allmendinger, G. Ross, J. Kolb, C. Burdack, M. Umkehrer, "Tetramic acid derivatives via Ugi-Dieckmann-reaction" Tetrahedron Lett., 2009, 50, 1705-1707. (DOI)

9. V. Knorr, V. Russ, L. Allmendinger, M. Ogris, E. Wagner, "Acetal Linked Oligoethylenimines for Use As pH-Sensitive Gene Carriers" Bioconjugate Chem., 2008, 19, 1625–1634. (DOI)

8. V. Knorr, L. Allmendinger, G. F. Walker, F. F. Paintner, E. Wagner, "An Acetal-Based PEGylation Reagent for pH-Sensitive Shielding of DNA Polyplexes" Bioconjugate Chem., 2007, 18, 1218-1225. (DOI)



7. F. F. Paintner, L. Allmendinger, G. Bauschke, "A New, General Method for the Highly Regioselective Introduction of Substiutents into the 3-Position of 5-Unsubstituted 4-O-Alkyl Tetronates" Synlett, 2005, 18, 2735-2738. (DOI)



6. L. Allmendinger, G. Bauschke, F. F. Paintner, "Total Synthesis of Sperabilin A and C" Synlett, 2005, 17, 2615-2618. (DOI)



5. F. F. Paintner, L. Allmendinger, G. Bauschke, P. Klemann, "Highly Efficient Approach to Orthogonally Protected (2S,4R)- and (2S,4S)-4-Hydroxyornithine" Org. Lett., 2005, 7, 1423-1426. (DOI)

4. F. F. Paintner, L. Allmendinger, G. Bauschke, C. Berns, P. Heisig, "Synthesis and Antimicrobial Activity of Tetrodecamycin Partial Structures" Bioorg. & Med. Chem., 2003, 11, 2823-2833. (DOI)



3. F. F. Paintner, L. Allmendinger, G. Bauschke, "Highly Efficient 4-O-Alkylations of Tetronic Acids Involving Oxyphosphonium Intermediates" Synlett, 2003, 1, 83-86. (DOI)



2. F. F. Paintner, L. Allmendinger, G. Bauschke, K. Polborn, "Synthetic Studies toward Tetrodecamycin: An Efficient Approach to the Core Structure of the Antibiotic" Synlett, 2002, 8, 1308-1312. (DOI)

1. F. F. Paintner, L. Allmendinger, G. Bauschke, "Highly Regioselective 3-Hydroxyalkylations of Boron 4-Methoxy-2-furanolates: A New Entry to 5-Unsubstituted and 5-Monosubstituted 3-Acyl-4-O-Methyl Tetronates" Synthesis, 2001, 14, 2113-2118. (DOI)



Druckansicht - Impressum - Datenschutz - Kontakt - Log In