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Chemical Communications (Cambridge, England)|August 29, 2002
Development of new acid-functionalized resins for combinatorial synthesis on solid supportsFrank Stieber, Herbert WaldmannChemistry (Weinheim an Der Bergstrasse, Germany)|July 17, 2003
Development of the traceless phenylhydrazide linker for solid-phase synthesisFrank Stieber, Uwe Grether, Herbert WaldmannBioorganic & Medicinal Chemistry Letters|June 1, 2002
Syntheses of depsipeptide analogues of the insect neuropeptide proctolinJürgen Scherkenbeck, Andrew Plant, Frank Stieber, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|July 17, 2003
Multistep solid-phase synthesis of an antibiotic and receptor tyrosine kinase inhibitors using the traceless phenylhydrazide linkerFrank Stieber, Uwe Grether, Ralph Mazitschek, et al.Bioorganic & Medicinal Chemistry Letters|March 23, 2011
Design and synthesis of isoquinolines and benzimidazoles as RAF kinase inhibitorsHans-Peter Buchstaller, Lars Burgdorf, Dirk Finsinger, et al.Bioorganic & Medicinal Chemistry Letters|March 5, 2015
Identification and optimization of pyridazinones as potent and selective c-Met kinase inhibitorsDieter Dorsch, Oliver Schadt, Frank Stieber, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 5, 2013
EMD 1214063 and EMD 1204831 constitute a new class of potent and highly selective c-Met inhibitorsFriedhelm Bladt, Bettina Faden, Manja Friese-Hamim, et al.Journal of Medicinal Chemistry|January 23, 2016
Discovery of Potent, Selective, and Orally Bioavailable Small-Molecule Modulators of the Mediator Complex-Associated Kinases CDK8 and CDK19Aurélie Mallinger, Kai Schiemann, Christian Rink, et al.Journal of Medicinal Chemistry|February 14, 2015
Discovery of potent, orally bioavailable, small-molecule inhibitors of WNT signaling from a cell-based pathway screenAurélie Mallinger, Simon Crumpler, Mark Pichowicz, et al.Pageof 1