Radkowski, K.; Fürstner, A. A Sphingolipid Fatty Acid Constituent Made by Alkyne Trans-Hydrogenation: Total Synthesis of Symbioramide. Advanced Synthesis & Catalysis2022, 364, 3342–3347.
Huwyler, N.; Radkowski, K.; Rummelt, S. M.; Fürstner, A. Two Enabling Strategies for the Stereoselective Conversion of Internal Alkynes into Trisubstituted Alkenes. Chemistry – A European Journal2017, 23, 12412–12419.
Rummelt, S. M.; Radkowski, K.; Roşca, D.-A.; Fürstner, A. Interligand Interactions Dictate the Regioselectivity of Trans-Hydrometalations and Related Reactions Catalyzed by [Cp*RuCl]. Hydrogen Bonding to a Chloride Ligand as a Steering Principle in Catalysis. Journal of the American Chemical Society2015, 137, 5506–5519.
Radkowski, K.; Sundararaju, B.; Fürstner, A. A Functional-Group-Tolerant Catalytic Trans Hydrogenation of Alkynes. Angewandte Chemie International Edition2013, 52, 355–360.
Fürstner, A.; Radkowski, K.; Peters, H. Chasing a Phantom by Total Synthesis: The Butylcycloheptylprodigiosin Case. Angewandte Chemie International Edition2005, 44, 2777–2781.
Lacombe, F.; Radkowski, K.; Seidel, G.; Fürstner, A. (E)-Cycloalkenes and (E,E)-Cycloalkadienes by Ring Closing Diyne- or Enyne–Yne Metathesis/Semi-Reduction. Tetrahedron2004, 60, 7315–7324.
Fürstner, A.; Radkowski, K. A Chemo- and Stereoselective Reduction of Cycloalkynes to (E)- Cycloalkenes. Chemical Communications2002, No. 18, 2182–2183.
Prof. Ferdi Schüth has been named an honorary fellow of the Chinese Chemical Society for his contributions to sustainable catalysis and international collaboration.
To mark the 100th anniversary of the Fischer-Tropsch synthesis, a scientific conference will be held in Mülheim next year. Our institute will of course be taking part.