Sascha Jautze

Practical, Highly Active, and Enantioselective Ferrocenyl–Imidazoline Palladacycle Catalysts (FIPs) for the Aza‐Claisen Rearrangement of <i>N</i>‐<i>para</i>‐Methoxyphenyl Trifluoroacetimidates

Matthias E. Weiss, Daniel F. Fischer, Zhuo‐Qun Xin et al. · Angewandte Chemie International Edition · 2006 · 136 citations

Chemical Engineering, Cross-coupling Reaction, Engineering +15

Enantioselective Bimetallic Catalysis of Michael Additions Forming Quaternary Stereocenters

Sascha Jautze, René Peters · Angewandte Chemie International Edition · 2008 · 133 citations

Enantioselective Synthesis, Engineering, Natural Sciences +12

Bispalladacycle-Catalyzed Brønsted Acid/Base-Promoted Asymmetric Tandem Azlactone Formation−Michael Addition

Manuel Weber, Sascha Jautze, Wolfgang Frey et al. · Journal of the American Chemical Society · 2010 · 124 citations

Macrocyclic Ferrocenyl–Bisimidazoline Palladacycle Dimers as Highly Active and Enantioselective Catalysts for the Aza‐Claisen Rearrangement of <i>Z</i>‐Configured <i>N</i>‐<i>para</i>‐Methoxyphenyl Trifluoroacetimidates

Sascha Jautze, Paul Seiler, René Peters · Angewandte Chemie International Edition · 2007 · 111 citations

Chemical Engineering, Enantioselective Catalysts, Engineering +15

Asymmetric Michael additions of α-cyanoacetates by soft Lewis acid/hard Brønsted acid catalysis: stereodivergency with bi- vs. monometallic catalysts

Simon H. Eitel, Sascha Jautze, Wolfgang Frey et al. · Chemical Science · 2013 · 79 citations

Asymmetric Catalysis, Cross-coupling Reaction, Engineering +14