Hydrostannylierungen

  • U. Kazmaier, D. Schauß, M. Pohlman, "Mo(CO)3(CNtBu)3, a new Efficient Catalyst for Regioselective Hydrostannations", Org. Lett. 1999; 1, 1017-1019.
  • U. Kazmaier, D. Schauß, M. Pohlman, S. Raddatz, "Application of the Molybdenum-Catalysed Hydrostannation towards a Flexible Synthesis of Substituted Unsaturated Amino Acids", Synthesis 2000, 914-916.
  • U. Kazmaier,M. Pohlman, D. Schauß, "Regioselective Hydrostannations Using Mo(CO)3(CNtBu)3 (MoBI3) as a New, Efficient Catalyst", Eur. J. Org. Chem. 2000, 2761-2766.
  • U. Kazmaier, D. Schauß, S. Raddatz, M. Pohlman, "Preparation and Reactions of Stannylated Amino Acids", Chem. Eur. J. 2001, 7, 456-464.
  • S. Braune, U. Kazmaier, "Regioselective hydrostannations catalyzed by molybdenum isonitrile complexes", J. Organomet. Chem. 2002, 641,26-29.
  • S. Braune, U. Kazmaier, "Entwicklung eines neuen Katalysators zur Distannylierung von Alkinen", Angew. Chem. 2003, 115, 318-320; Angew. Chem. Int Ed. 2003, 42, 306-308.
  • S. Braune, M. Pohlman, U. Kazmaier, "Molybdenum-catalyzed Stannylations as Key Steps in Heterocyclic Synthesis", J. Org. Chem. 2004, 69, 468-474.
  • U. Kazmaier, M. Klein, "Molybdenum-Catalyzed Hydrostannations of Allenoles", Chem. Commun. 2005, 501-503.
  • U. Kazmaier, A. Wesquet, "Stannylated allylsulfones as versatile new building blocks", Synlett 2005,1271-1274.
  • S. Dörrenbächer, U. Kazmaier, S. Ruf, "A Straightforward Approach towards Piperidines via Stille Coupling and subsequent 1,4-Addition of Amines", Synlett 2006, 547-550.
  • U. Kazmaier, S. Lucas, M. Klein, "Syntheses and synthetic applications of stannylated allylic alcohols", J. Org. Chem. 2006, 71, 2429-2433.
  • U. Kazmaier, S. Dörrenbächer, A. Wesquet, S. Lucas, M. Kummeter, "Molybdenum-catalyzed Synthesis of Stannylated Allylic Alcohol Derivatives and their Synthetic Applications", Synthesis 2007, 320-326.
  • H. Lin, U. Kazmaier, "Regioselective Mo-catalyzed hydrostannations as key steps in the synthesis of functionalized amino alcohols and heterocycles", Eur. J. Org. Chem. 2007, 2839-2843.
  • 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.
  • A. O. Wesquet, U. Kazmaier, "Distannylierung und Silastannylierung in situ generierter Allene", Angew. Chem. 2008, 120, 3093-3096; Angew. Chem. Int. Ed. 2008, 47, 3050-3053.
  • N. Jena, U. Kazmaier, "Synthesis of stannylated allyl and vinyl phosphonates via Molybdenum catalyzed hydrostannations", Eur. J. Org. Chem. 2008, 3852-3858.
  • H. Lin, U. Kazmaier, "Molybdenum-Catalyzed α-Hydrostannations of Propargyl Amines as Key Step for the Synthesis of N-Heterocycles", Eur. J. Org. Chem. 2009, 1221-1227.
  • A. O. Wesquet, U. Kazmaier, "Improved Protocols for Molybdenum- und Tungsten-catalyzed Hydrostannations", Adv. Synth. Catal. 2009, 1395–1404.
  • C. Bukovec, U. Kazmaier, "A Straightforward Protocol for One-pot Allylic Aminations/Stille Couplings", Org. Lett. 2009, 11, 3518–3521.
  • B. V. Lakshmi, U. Kazmaier, "A straightforward approach towards substituted Morita-Baylis-Hillman (MBH) products via hydrostannation of acetylenic ketones", Synlett 2010, 407–410.
  • R. Pratap, U. Kazmaier, "Synthesis of 1-Stannylated and Iodinated 1-Chloroalkenes as Versatile Synthetic Intermediates", Synlett 2010, 3073–3077.
  • B. V. Lakshmi, U. K. Wefelscheid, U. Kazmaier, "Synthesis of Arylstannanes from Silyl Triflates via Aryne Intermediates", Synlett 2011, 345–348.
  • C. Bukovec, A. O. Wesquet, U. Kazmaier, "Insights into the Reaction Behaviour of Stannylated Allylic Substrates", Eur. J. Org. Chem. 2011, 1047–1056.
  • C. Bukovec, U. Kazmaier, "Stannylated allyl carbonates as versatile building blocks for the diversity oriented synthesis of allylic amines and amides", Org. Biomol. Chem. 2011, 9, 2743–2750.
  • M. Klos, U. Kazmaier, "A Catalyst-Economic One-Pot Protocol for the Synthesis and Conversion of Functionalized Vinylstannanes", Eur. J. Org. Chem. 2013, 1726–1731.