Modifizierung von Peptiden

  • U. Kazmaier, "Introduction of Allylic Side Chains onto Peptides by Pd(0)-Catalyzed Ester Enolate Claisen Rearrangement", J. Org. Chem. 1994, 59, 6667-6670.
  • U. Kazmaier, S. Maier, "Application of the Chelate Enolate Claisen Rearrangement to the Modification of Peptides", J. Chem. Soc., Chem. Commun. 1998, 2535-2536.
  • U. Kazmaier, S. Maier, "Stereoselective Backbone Modifications of Peptides using Peptide Metal Complexes", J. Org. Chem. 1999, 64, 4574-4575.
  • U. Kazmaier, S. Maier, "Application of the Peptide Claisen Rearrangement towards the Synthesis of Cyclic Peptides", Org. Lett. 1999, 1, 1763-1766.
  • S. Maier, U. Kazmaier, "Modifications of Peptides via Chelate Claisen Rearrangements of Manganese Enolates", Eur. J. Org. Chem. 2000, 1241-1251.
  • U. Kazmaier, S. Maier, F. L. Zumpe, "A Journey from Amino Acid and Peptide Chemistry to Palladium and Back", Synlett 2000, 1523-1535.
  • U. Kazmaier, J. Deska, A. Watzke, "Stereoselektive Palladium-katalysierte Allylierung von Peptiden", Angew. Chem. 2006, 118, 4973-4976; Angew. Chem. Int. Ed. 2006, 45, 4855-4858.
  • J. Deska, U. Kazmaier, "Stereoselektive Synthese und Umsetzung stannylierter Peptide", Angew. Chem. 2007, 119, 4654-4657; Angew. Chem. Int. Ed. 2007, 46, 4570-4573.
  • J. Deska, U. Kazmaier, "Highly Stereoselective Peptide Modifications via Palladium Cataly­zed Allylic Alkylations of Chelated Peptide Enolates", Chem. Eur. J. 2007, 13, 6204-6211.
  • S. Datta, U. Kazmaier, "Stereoselective palladium-catalyzed allylic alkylations of peptide amide enolates", Org. Biomol. Chem. 2011, 9, 872–880.
  • S. Datta, A. Bayer, U. Kazmaier, "Highly Stereoselective Modifications of Peptides via Pd-catalyzed Allylic Alkylation of Internal Peptide Amide Enolates", Org. Biomol. Chem. 2012, 10, 8268–8275.
  • U. Kazmaier, A. Bayer, J. Deska, "Palladium-catalyzed Allylic Alkylations as Versatile Tool in Amino Acid and Peptide Modifications", Synthesis 2013, 45, 1462–1468.
  • A. Bayer, U. Kazmaier, "Selective Peptide Modifications via Ruthenium-catalyzed Allylic Alkylations", J. Org. Chem. 2014, 79, 8491–8497.