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, Nr. 18, 2182–2183.