Michael additions of chelated amino ester enolates

  • M. Pohlman, U. Kazmaier, "Efficient Stereoselective Syntheses of Cyclic Amino Acids via Michael Induced Ring Closing Reactions", Org. Lett. 2003, 5, 2631-2633.
  • M. Pohlman, U. Kazmaier, T. Lindner, "Allylic Alkylation versus Michael induced Ring Closure – Chelated Enolates as versatile Nucleophiles", J. Org. Chem. 2004, 69, 6909-6912.
  • B. Mendler, U. Kazmaier, "Stereoselective Additions of Tin Enolates to Nitroalkenes and their Subsequent Conversion into Nitriles", Org. Lett. 2005, 7, 1715-1718.
  • B. Mendler, U. Kazmaier, V. Huch, M. Veith, "A straightforward approach to iminoxazines and azetidin­imines via 1,4-additions of chelated enolates towards nitroalkenes", Org. Lett. 2005, 7, 2643-2646.
  • B. Mendler, U. Kazmaier, "Diastereoselective Michael Additions of Chelated Enolates towards Nitroalkenes", Synthesis 2005, 2239-2245.
  • S. Lucas, U. Kazmaier, "Allenyl ketones as versatile Michael acceptors for the addition of chelated enolates", Synlett 2006, 255-258.
  • C. Schmidt, U. Kazmaier, "Efficient Stereoselective Syntheses of Constrained Glutamates via Michael Induced Ring Closing Reactions", Eur. J. Org. Chem. 2008, 887-894.
  • C. Schmidt, U. Kazmaier, "Synthesis of highly substituted pyroglutamates via a domino Michael addition / Claisen rearrangement / lactamization approach", Org. Biomol. Chem. 2008, 6, 4643-4648.
  • U. Kazmaier, C. Schmidt, "Synthesis of Highly Functionalized Proline Derivatives via a One-pot Michael-/Aldol-Addition/Cyclization-Approach", Synlett 2009, 1136-1140.
  • U. Kazmaier, C. Schmidt, "Synthesis of Highly Functionalized Proline Derivatives via a One-Pot Michael-/SN’-Addition/Cyclization-Approach", Synthesis 2009, 2435–2439.
  • U. Kazmaier, C. Schmidt, "Synthesis of Furanoid Amino Acids via a Domino Michael-/ Aldol-Addition/Cyclization-Approach", Synlett 2009, 2625–2628.
  • L. Wirtz, U. Kazmaier, "A Straightforward Approach towards Isoxazoline Amino Acids via Domino Michael Addition / Nitrile Oxide Cycloaddition", Eur. J. Org. Chem. 2011, 3467–3474.