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Organic Letters|November 25, 2011
Expanding the azaspiro[3.3]heptane family: synthesis of novel highly functionalized building blocksJohannes A Burkhard, Carine Guérot, Henner Knust, et al.
Angewandte Chemie (International Ed. in English)|October 30, 2010
Oxetanes as versatile elements in drug discovery and synthesisJohannes A Burkhard, Georg Wuitschik, Mark Rogers-Evans, et al.
Organic Letters|April 2, 2010
Synthesis and structural analysis of a new class of azaspiro[3.3]heptanes as building blocks for medicinal chemistryJohannes A Burkhard, Carine Guérot, Henner Knust, et al.
Organic Letters|August 14, 2013
Synthesis and stability of oxetane analogs of thalidomide and lenalidomideJohannes A Burkhard, Georg Wuitschik, Jean-Marc Plancher, et al.
Chemmedchem|October 23, 2009
Synthesis, inhibition potency, binding mode, and antiprotozoal activities of fluorescent inhibitors of trypanothione reductase based on mepacrine-conjugated diaryl sulfide scaffoldsChristian Eberle, Johannes A Burkhard, Bernhard Stump, et al.
Organic Letters|July 24, 2025
Stereoselective Synthesis of trans-3-Amino-2,2,4,4-tetramethylcyclobutanolDaniel Zell, Guy Pillon, Hans Iding, et al.
Organic Letters|May 10, 2023
Second-Generation Atroposelective Synthesis of KRAS G12C Covalent Inhibitor GDC-6036Jie Xu, Ngiap-Kie Lim, Jacob C Timmerman, et al.
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