Allylische Alkylierungen chelatverbrückter Aminosäureesterenolate

  • 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, F. L. Zumpe, "Chelatisierte Aminosäureesterenolate - Effiziente Nukleo­phile für Palladium-katalysierte Allylische Alkylierungen", Angew. Chem. 1999, 111, 1572-1574; Angew. Chem. Int. Ed. Engl. 1999, 38, 1468-1470.
  • U. Kazmaier, F. L. Zumpe, "Isomerisierungsfreie Palladium-katalysierte Allylierungen – Wunsch oder Wirklichkeit?", Angew. Chem. 2000, 112, 805-807; Angew. Chem. Int. Ed. Engl. 2000, 39, 802-804.
  • 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, F. L. Zumpe, "Chelated Enolates of Amino Acid Esters – new Efficient Nucleo­philes for Isomerization-free Stereoselective Palladium-Catalyzed Allylic Substitutions", Eur. J. Org. Chem. 2001, 4067-4076.
  • T. D. Weiß, G. Helmchen, U. Kazmaier, "Synthesis of amino acid derivatives via enantio- and diastereoselective Pd-catalyzed allylic substitutions with a non-stabilized enolate as nucleophile", J. Chem. Soc. Chem. Commun. 2002, 1270-1271.
  • U. Kazmaier, M. Pohlman, "Regioselective palladium catalyzed allylic alkylations via anti/syn-π-allyl intermediates", Synlett 2004, 623-626.
  • U. Kazmaier, T. Lindner, "Effizienter 1,5-Chiralitätstransfer bei Palladium-katalysierten allylischen Alkylierungen chelatisierter Aminosäureesterenolate", Angew. Chem. 2005, 117, 3368-3371; Angew. Chem. Int. Ed. 2005, 44, 3303-3306.
  • M. Bauer, U. Kazmaier, "Synthesis of γ,δ-unsaturated amino acids via palladium-catalyzed allylic alkylation of chelated glycin ester enolates", Recent Res. Devel. in Organic Chem. 2005, 9, 49-69.
  • T. Lindner, U. Kazmaier, "Substrate controlled palladium catalyzed allylic alkylations of chelated enolates – scope and limitations", Adv. Synth. Catal. 2005, 347, 1687-1695.
  • 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.
  • K. Krämer, U. Kazmaier, "Isomerisierungsfreie Allylische Alkylierungen via terminale π-Allyl-Palladium-Komplexe", J. Org. Chem. 2006,71, 8950-8953.
  • 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.
  • U. Kazmaier, D. Stolz, K. Krämer, F. Zumpe, "Influences on the Regioselectivity of Palladium-catalyzed Allylic Alkylations", Chem. Eur. J. 2008, 14, 1322-1329.
  • D. Stolz, U. Kazmaier, "Rhodium-Catalyzed Allylic Alkylations as Key Steps in the Synthesis of Cyclic α-Alkylated Amino Acids", Synthesis 2008, 2288–2292.
  • S. Basak, U. Kazmaier, "Palladium-catalyzed Dienylations of Chelated Enolates", Eur. J. Org. Chem. 2008, 4169-4177.
  • K. Krämer, J. Deska, C. Hebach, U. Kazmaier, "A straightforward approach towards glycoamino acids and glycopeptides via Pd-catalysed allylic alkylation", Org. Biomol. Chem. 2009, 7, 103-110.
  • S. Thies, U. Kazmaier, "Vinylepoxides as Versatile Substrates for Allylations of Amino Acids and Peptides", Synlett 2010, 137–141.
  • D. Gawas, U. Kazmaier, "Diastereotopos-differentiating allylic alkylation as key step in natural product synthesis", Org. Biomol. Chem. 2010, 8, 457–462.
  • A. Bayer, U. Kazmaier, "Highly Regioselective Ruthenium-catalyzed Allylic Alkylations of Chelated Enolates", Org. Lett. 2010, 12, 4960–4963.
  • S. Datta, U. Kazmaier, "Stereoselective palladium-catalyzed allylic alkylations of peptide amide enolates", Org. Biomol. Chem. 2011, 9, 872–880.
  • S. Hähn, U. Kazmaier, "Chemoselective Rh-Catalyzed Allylic Alkylations of Chelated Enolates using Dienylcarbonates", Eur. J. Org. Chem. 2011, 4931–4939.
  • 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.
  • J. Gorges, A. Ullrich, U. Kazmaier, "A Straightforward Approach towards Ferrocenyl Amino Acids and Peptides via Allylic Alkylation", Eur. J. Org. Chem. 2013, 4372–4378.
  • S. Thies, U. Kazmaier, "Synthesis of α-Amino-γ-lactones via Pd-catalyzed intramolecular allylic alkylation of sarcosine allyl amides", Eur. J. Org. Chem. 2014, 1695–1707.
  • A. Bayer, U. Kazmaier, "[(p-cymene)RuCl2]2, an Efficient Catalyst for Highly Regioselective Allylic Alkylations of Chelated Amino Acid Ester Enolates", Chem. Eur. J. 2014, 20, 10484–10491.
  • A. Bayer, U. Kazmaier, "Selective Peptide Modifications via Ruthenium-catalyzed Allylic Alkylations", J. Org. Chem. 2014, 79, 8491–8497.
  • A. Bayer, U. Kazmaier, "Ruthenium-catalyzed Allylic Alkylations of Chelated Enolates using Vinyl Dioxolanon-2-ones", J. Org. Chem. 2014, 79, 8498−8504.
  • P. Servatius, U. Kazmaier, "A straightforward approach towards functionalized amino acids and pipecolinic acids via Ru-catalyzed allylic alkylation", Synlett 2015, 26, 2001–2005.