Markus Bänziger

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The development of a practical synthesis of the potent and selective somatostatin sst3 receptor antagonist [4-(3,4-difluoro-phenyl)-piperazine-1-yl]-{(4S,4aS,8aR)-2[(S)-3-(6-methoxy-pyridin-3-yl)-2-methyl-propyl]-decahydroisoquinoline-4-yl}-methanone (NVP-ACQ090)

T. Troxler, C. Malan, F. Spindler, 2003 .

Development and Scale-Up of the Electrochemical Dehalogenation for the Synthesis of a Key Intermediate for NS5A Inhibitors

Siegfried R. Waldvogel, S. Waldvogel, C. Bucher, 2015 .

A Novel Cathode Material for Cathodic Dehalogenation of 1,1-Dibromo Cyclopropane Derivatives.

Fabrice Gallou, Siegfried R Waldvogel, S. Waldvogel, 2015, Chemistry.

An Alternative Synthesis of the Enantiomerically Pure Competitive NMIDA Antagonists SDZ 220-581 and SDZ EAB 515

P. Kipfer, W. Müller, Markus Bänziger, 1998 .

The Synthesis of a Novel Inhibitor of B-Raf Kinase

T. Ramsey, L. Perez, D. Batt, 2006 .

Synthesis and Determination of the Absolute Configuration of (+)‐Delesserine, a Metabolite of the Red Marine Alga Delesseria sanguinea (Lamouroux)

D. Seebach, R. Naef, Markus Bänziger, 1984 .

Practical and Large-Scale Synthesis of rac-(3S,4aR,10aR)- 6-Methoxy-1-propyl-1,2,3,4,4a,5,10,10a-octahydrobenzo[g]quinoline-3-carboxylic Acid Methyl Ester

U. Sunay, J. Cercus, Markus Bänziger, 2000 .

A New Practical Route for the Manufacture of (4aR,10aR)-9-Methoxy-1-methyl-6-trimethylsilanyl- 1,2,3,4,4a,5,10,10a-octahydrobenzo[g]quinoline

L. Vecchia, J. Nozulak, E. Küsters, 2003 .

An Efficient Synthesis of Racemic 4‐Hydroxy‐2‐oxo‐1‐pyrrolidineacetamide (Oxiracetam) Using Tetramic‐Acid Intermediates

T. Meul, A. R. Evans, Markus Bänziger, 1992 .