K. Wanner

发表

Rigid nonproteinogenic cyclic amino acids as ligands for glutamate receptors: trans-tris(homoglutamic) acids.

G. Höfner, H. Bräuner‐Osborne, U. Madsen, 2005, Chirality.

Synthesis, biological evaluation and structure-activity relationship of new GABA uptake inhibitors, derivatives of 4-aminobutanamides.

G. Höfner, K. Kulig, A. Rapacz, 2014, European journal of medicinal chemistry.

In vitro pharmacological characterization of the bispyridinium non-oxime compound MB327 and its 2- and 3-regioisomers.

G. Höfner, F. Worek, T. Seeger, 2017, Toxicology letters.

Chiral N-acyliminium ions as new tools in the asymmetric synthesis of CNS-active compounds

K. Wanner, 1994 .

A general approach to substituted diphenyldiazenes

K. T. Wanner, Toni A. Lutz, Patrick Spanner, 2016 .

Asymmetric synthesis of all four stereoisomers of 1-amino-3-hydroxy-cyclopentane-1-carboxylic acid

K. Kulig, M. Żylewski, A. Jakubowska, 2015 .

Conjugate Addition of Organomagnesium Cuprates to Guvacine Derivatives

K. T. Wanner, Tim Hellenbrand, K. Wanner, 2014 .

Characterisation of the binding of [3H]MDL 105,519, a radiolabelled antagonist for the N-methyl-d-aspartate-associated glycine site, to pig cortical brain membranes

G. Höfner, K. T. Wanner, K. Wanner, 1997, Neuroscience Letters.

Electrophysiological investigation of the effect of structurally different bispyridinium non-oxime compounds on human α7-nicotinic acetylcholine receptor activity-An in vitro structure-activity analysis.

Franz Worek, Thomas Seeger, Horst Thiermann, 2017, Toxicology letters.

Generation of a 3D model for human GABA transporter hGAT-1 using molecular modeling and investigation of the binding of GABA

K. T. Wanner, T. Wein, K. Wanner, 2010, Journal of molecular modeling.

Determination of enantiomeric excess of nipecotic acid as 1-(7-nitrobenzo[c][1,2,5]oxadiazol-4-yl) derivatives.

G. Höfner, Simone Schmidt, K. Wanner, 2017, Chirality.

Novel mouse GABA uptake inhibitors with enhanced inhibitory activity toward mGAT3/4 and their effect on pain threshold in mice.

G. Höfner, B. Malawska, A. Nowaczyk, 2019, European journal of medicinal chemistry.

Asymmetric Electrophilic α‐Amidoalkylation, VII1): Generation, Crystal Structure, and Trapping Reactions of a Chiral 6,7‐Dimethoxy‐1,2,3,4‐tetrahydroisoquinoline Derived N‐Acyliminium Ion

U. Nagel, K. T. Wanner, I. Praschak, 1990 .

Counteracting desensitization of human α7-nicotinic acetylcholine receptors with bispyridinium compounds as an approach against organophosphorus poisoning.

F. Worek, T. Seeger, H. Thiermann, 2017, Toxicology letters.

Regioselective and Transition-Metal-Free Addition of tert-Butyl Magnesium Reagents to Pyridine Derivatives: A Convenient Method for the Synthesis of 3-Substituted 4-tert-Butylpyridine Derivatives

F. Worek, T. Seeger, H. Thiermann, 2017, Synthesis.

Synthesen und Ringverengungsreaktionen α‐halogenierter N‐Phenylcamphersäureimide

K. Wanner, 1988 .

PYRANS, 100. 5,6‐DIHYDRO‐2H‐PYRAN‐3(4H)‐ONE AS A SYNTHON FOR PYRAN‐ANNULATED HETEROCYCLIC COMPOUNDS

F. Eiden, K. Wanner, 1985 .

Electrocyclic ring-opening reactions may cause failure of enolate alkylation of 1,4-oxazin-2-one based chiral glycine equivalents

K. Wanner, Sofia Simonyiova, 2008 .

The Glutamic Acid-Rich Protein Is a Gating Inhibitor of Cyclic Nucleotide-Gated Channels

M. Biel, E. Becirovic, S. Michalakis, 2011, The Journal of Neuroscience.

Application of an Ugi type reaction to an N-silyl-4,4-disubstituted 1,4-dihydropyridine

P. Mayer, K. T. Wanner, Christian A. Sperger, 2009 .

Diastereoselective synthesis of β-amino acid derivatives from dihydropyridones

K. T. Wanner, Markus Ege, K. Wanner, 2008 .

Determination of the enantiomeric purity of the selective dopamine transporter inhibitor (+)-R,R-4-(2-benzhydryloxyethyl)-1-(4-fluorobenzyl)piperidin-3-ol.

G. Höfner, Patrick Neiens, K. Wanner, 2017, Chirality.

CYCLOBUTANONE-ENAMINES: SYNTHESIS AND REACTIONS OF N-(1-CYCLOBUTENYL)PIPERIDINE

A. Kaertner, K. Wanner, 1985 .

Construction of 4-substituted 2-(pyrrolidine-3-yl)acetic acid derivatives as cyclic γ-aminobutyric acid analogues employing intermolecular [2+2]-photocycloaddition as key steps

L. Allmendinger, P. Mayer, K. Wanner, 2019, Tetrahedron.

Synthesis and pharmacological properties of new GABA uptake inhibitors

G. Höfner, B. Malawska, K. Kulig, 2012, Pharmacological reports : PR.

(1R,3S,6S)-6-tert-Butyl-1-hydroxymethyl-5-methoxy-6-methyl-7-oxa-4-azaspiro[2.5]oct-4-en-8-one and dimethyl [(1S,1'R,3'S,6'S)-(6'-tert-butyl-5'-methoxy-6'-methyl-8'-oxo-7'-oxa-4'-azaspiro[2.5]oct-4'-en-1'-yl)hydroxymethyl]phosphonate.

M. Małecka, E. Budzisz, K. Wanner, 2003, Acta crystallographica. Section C, Crystal structure communications.

Asymmetric Synthesis and Enantioselectivity of Binding of 1‐Aryl‐1,2,3,4‐tetrahydroisoquinolines at the PCP Site of the NMDA Receptor Complex

G. Höfner, K. T. Wanner, H. Beer, 1998 .

Camphoric acid derived sulfur containing bicyclic carboxylic acids as chiral auxiliaries in N-acyliminium ion chemistry

P. Mayer, K. Polborn, Jörg Pabel, 2010 .

Direct Synthesis of 4,4‐Disubstituted N‐Silyl‐1,4‐dihydropyridines.

K. Wanner, Jan Braeckow, 2006 .

Direct synthesis of 4,4-disubstituted N-silyl-1,4-dihydropyridines

K. T. Wanner, J. Bräckow, K. Wanner, 2006 .

[3H]ifenprodil binding to NMDA receptors in porcine hippocampal brain membranes.

G. Höfner, K. Wanner, 2000, European journal of pharmacology.

Synthesis and resolution of racemic eliprodil and evaluation of the enantiomers of eliprodil as NMDA receptor antagonists.

G. Höfner, J. Pabel, K. Wanner, 2000, Bioorganic & medicinal chemistry letters.

Characterisation of [3H]MK-801 binding and its cooperative modulation by pig brain membranes.

G. Höfner, K. T. Wanner, K. Wanner, 1996, Journal of receptor and signal transduction research.

New Resensitizers for the Nicotinic Acetylcholine Receptor by Ligand-Based Pharmacophore Modeling.

F. Worek, T. Seeger, H. Thiermann, 2018, Current computer-aided drug design.