0000-0002-7371-8481 About
Education
Sep 1993 - Oct 2000: M.Sc. (DI), Technical Chemistry / Organic Chemistry and Technology, Vienna University of Technology, Prof. Peter Gaertner, Thesis: “Investigations on arylsubstituted hydrobenzoins as chiral auxiliaries”
Oct 2000 – Jul 2004: PhD (Dr tech), Vienna University of Technology, Prof. Peter Gaertner, Thesis: “Arylsubstituted meso-hydrobenzoins as new chiral auxiliaries and enantiopure linkers for stereo selective synthesis on solid phase”
Experience
Jul/Aug 1999 & Jul/Aug 2000: Trainee, Medicinal Chemistry, Bayer AG, Wuppertal
Mar 2000 – Feb 2001: Student Assistant, Institute of Applied Synthetic Chemistry, Vienna University of Technology
Jun 2001 – Aug 2004: Assistant, Institute of Applied Synthetic Chemistry, Vienna University of Technology
Sep 2004 – Aug 2006: Postdoctoral Position, Medicinal Chemistry (Oncology), Boehringer-Ingelheim, Vienna
Aug 2006 – Sep 2012: Scientist, Medicinal Chemistry (Oncology), Boehringer-Ingelheim, Vienna
May 2009 – Aug 2009: Scientist, Medicinal Chemistry (Virology), Boehringer-Ingelheim, Laval, Canada
May 2019 – July 2019: Visiting Scientist, Ciulli Laboratory, School of Life Sciences, University of Dundee
Sep 2012 – to date: Principal Scientist, Medicinal Chemistry (Oncology), Boehringer-Ingelheim, Vienna
Employment
Employment history is unavailable.
Education
Education history is unavailable.
Projects & Funding
Projects & funding information is unavailable.
Publications (8)
- Discovery of BI-2493, a Pan-KRAS Inhibitor Showing In Vivo Efficacy Save
- Fragment Optimization of Reversible Binding to the Switch II Pocket on KRAS Leads to a Potent, In Vivo Active KRASG12C Inhibitor Save
- Targeted Synthesis of Complex Spiro[3 H ‐indole‐3,2′‐pyrrolidin]‐2(1 H )‐ones by Intramolecular Cyclization of Azomethine Ylides: Highly Potent MDM2–p53 Inhibitors Save
- Chiral linker 5: scope and limitations of arylsubstituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for diastereoselective syntheses Save
- Discovery of Quinazolines as Histamine H4 Receptor Inverse Agonists Using a Scaffold Hopping Approach Save
- Chiral linker. Part 3: Synthesis and evaluation of aryl substituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for the diastereoselective reduction of α-keto esters Save
- Stereoselectivity in Pinacol-Homocoupling Mediated by Samarium Diiodide. Save
- Stereoselectivity in Pinacol-Homocoupling Mediated by Samarium Diiodide Save