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Dr. Andri Schütz

Dr. Andri Schütz

Dr. Andri Schütz

ZHAW School of Life Sciences and Facility Management
Fachgruppe Grundlagenchemie
Einsiedlerstrasse 31
8820 Wädenswil

+41 (0) 58 934 58 05
andri.schuetz@zhaw.ch

Personal profile

http://www.zhaw.ch/de/lsfm/institute-zentren/icbt/

Projects

Publications

Publications before appointment at the ZHAW

F. Hof, A. P. Schütz, C. Fäh, S. Meyer, D. Bur, J. Liu, D. E. Goldberg, F. Diederich, Angew. Chem., Int. Ed. 2006, 45, 2138–2141; Angew. Chem. 2006, 118, 2193–2196. Starving the malaria parasite: Inhibitors active against the aspartic proteases plasmepsins I, II, and IV.

M. Zürcher, F. Hof, L. Barandun, A. P. Schütz, W. B. Schweizer, S. Meyer, D. Bur, F. Diederich, Eur. J. Org. Chem. 2009, 11, 1701–1719. Synthesis of exo-3-amino-7-azabicyclo[2.2.1]heptanes as a class of malarial aspartic protease inhibitors: Exploration of two binding pockets.

A. P. Schütz, S. Osawa, J. Mathis, A. K. H. Hirsch, B. Bernet, B. Illarionov, M. Fischer, A. Bacher, F. Diederich, Eur. J. Org. Chem. 2012, 17, 3278–3287. Exploring the Ribose Sub-Pocket of the Substrate-Binding Site in Escherichia coli IspE: Structure-Based Design, Synthesis, and Biological Evaluation of Cytosines and Cytosine Analogues.

A. P. Schütz, S. Locher, B. Bernet, B. Illarionov, M. Fischer, A. Bacher, F. Diederich, Eur. J. Org. Chem. 2013, 5, 880–887. 5-Substituted (1-Thiolan-2-yl) cytosines as Inhibitors of A. aeolicus and E. coli IspE Kinases: Very Different Affinities to Similar Substrate-Binding Sites.

Z. Zheng, C. S. Ruiz-Vargas, T. Bauer, A. Rossi, P. Payamyar, A. P. Schütz, A. Stemmer, J. Sakamoto, A. D. Schlüter, Macromol. Rapid Commun. 2013, 34, 1670–1680. Square‐micrometer‐sized, free‐standing organometallic sheets and their square‐centimeter‐sized multilayers on solid substrates

P. Payamyar, K. Kaja, C. Ruiz-Vargas, A. Stemmer, D. J. Murray, C. J. Johnson, B. T. King, F. Schiffmann, J. VandeVondele, A. Renn, P. Ceroni, A. P. Schütz, L.-T. Lee, Z. Zheng, J. Sakamoto, A. D. Schlüter, Adv. Mat. 2014, 26, 2052–2058. Synthesis of a covalent monolayer sheet by photochemical anthracene dimerization at the air/water interface and its mechanical characterization by AFM indentation.

I. Gitsov, L. Wang, N. Vladimirov, A. Simonyan, A. P. Schütz, D. Kiemle, Biomacromolecules 2014, 15, 4082–4095. “Green” Synthesis of Unnatural Poly(Amino Acid)s with Zwitterionic Character and pH-Responsive Solution Behavior, Mediated by Linear-Dendritic Laccase Complexes.

P. Payamyar, M. Servalli, T. Hungerland, A. P. Schütz, Z. Zheng, A. Borgschulte, A. D. Schlüter, Macromol. Rapid Commun. 2014, accepted. Approaching Two-Dimensional Copolymers: Photoirradiation of anthracene- and diazanthracene-bearing monomers in a Langmuir monolayer.

L. Opilik, P. Payamyar, J. Szczerbinski, A. P. Schütz, M. Servalli, T. Hungerland, A D. Schlüter, R. Zenobi, ACS Nano 2015, 9, 4252–4259. Minimally-Invasive Characterization of Covalent Monolayer Sheets Using Tip-Enhanced Raman Spectroscopy”,

W. Dai, B. Zelenay, A. P. Schütz*, Z. Zheng, T. Keplinger, J. Sakamoto, A. D. Schlüter, in preparation. Synthesis of bipyridine- based oligofunctional monomers and their interfacial polymerization into novel metal-organic networks.