Unprecedented Strong Lewis Bases – Synthesis and Mehtyl Cation Affinities of Dimethylamino-Substituted Terpyridines P. Hommes, C. Fischer, C. Lindner, H. Zipse*, H.-U. Reißig* Angew. Chem. Int. Ed.2014, 53, 7647-7651.
Extrem starke Lewis-Basen - Synthese und Methylkationaffinitäten von Dimethylamino-substituierten Terpyridinen Paul Hommes, Christina Fischer, Christoph Lindner, Hendrik Zipse und Hans-Ulrich Reißig Angew. Chem.2014,126(29), 7778-7782.
Selektive katalytische Hydrodefluorierung als Schlüsselschritt zur Synthese bisher unzugänglicher Aminopyridinderivate G. Podolan, D. Lentz, H.U. Reißig Angew. Chem.2013, 125(36), 9669-9672.
Selective Catalytic Hydrodefluorination as a Key Step for the Synthesis of Hitherto Inaccessible Aminopyridine Derivatives G. Podolan, D. Lentz, H.U. Reissig Angew. Chem. Int. Ed.2013, 52(36), 9491-9494.
Synthesis of New Functionalized Calix[n]phyrin Macrocycles with Varied Ring Sizes by Using a Sterically Congested Dipyrromethane M. H. Beyzavi, D. Lentz, H.-U. Reissig, A. Wiehe Chem. Eur. J.2013, 19(20), 6203-6208.
Per(2-thienyl)pyridines: Synthesis and Properties Shivajirao L. Gholap, Paul Hommes, Katja Neuthe, Hans-Ulrich Reissig Org. Lett.2013, 15(2), 318-321.
The Influence of Perfluorinated Substituents on the Nucleophilic Reactivities of Silyl Enol Ethers H.A. Laub, D. Gladow, H.-U. Reissig, H. Mayr Org. Lett. 2012, 14(15), 3990-3993.
In Search of Oligo(2-thienyl)-Substituted Pyridine Derivatives: A Modular Approach to Di-, Tri- and Tetra(2-thienyl)pyridines Mrinal K. Bera, Paul Hommes, and Hans-Ulrich Reissig Chem. Eur. J. 2011, 17(42), 11838-11843.
Synthesis of 5-Acetyloxazoles and 1,2-Diketones from β-Alkoxy-β-ketoenamides and Their Subsequent Transformations T. Lechel, M. Gerhard, D. Trawny, B. Brusilowskij, L. Schefzig, R. Zimmer, J. P. Rabe, D. Lentz, C. A. Schalley, H.-U. Reißig* Chem. Eur. J. 2011, 17(27), 7480-7491.
Eine kurze formale Strychnin-Totalsynthese mit einer Samariumdiiodid-induzierten Kaskadenreaktion als Schlüsselschritt Christine Beemelmanns und Hans-Ulrich Reißig Angew. Chem. 2010, 122(43), 8195-8199.
A Short Formal Total Synthesis of Strychnine with a Samarium Diiodide Induced Cascade Reaction as the Key Step Christine Beemelmanns and Hans-Ulrich Reissig Angew. Chem. Int. Ed. 2010, 49(43), 8021-8025.
Three-Component Synthesis of Perfluoroalkyl- or Perfluoroaryl-Substituted 4-Hydroxypyridine Derivatives and Their Palladium-Catalyzed Coupling Reactions Tilman Lechel, Jyotirmayee Dash, Paul Hommes, Dieter Lentz, and Hans-Ulrich Reissig J. Org. Chem. 2010, 75(3), 726-732.
Nine Times Fluoride can be Good for your Syntheses. Not just Cheaper: Nonafluorobutanesulfonates as Intermediates for Transition Metal-Catalyzed Reactions Jens Högermeier, Hans-Ulrich Reissig Adv. Synth. Catal. 2009, 351(17), 2747-2763.
Three-Component Synthesis of Highly Functionalized 5-Acetyloxazoles Tilman Lechel, Dieter Lentz, and Hans-Ulrich Reissig Chem. Eur. J. 2009, 15(22), 5432-5435.
Stereodivergente De-novo-Synthese verzweigter Aminozucker durch Lewis-Säure-induzierte Umlagerung von 1,2-Oxazinen Fabian Pfrengle, Dieter Lentz und Hans-Ulrich Reißig Angew. Chem. 2009, 121(17), 3211-3215.
Stereodivergent De Novo Synthesis of Branched Amino Sugars by Lewis Acid Promoted Rearrangement of 1,2-Oxazines Fabian Pfrengle, Dieter Lentz, and Hans-Ulrich Reißig Angew. Chem. Int. Ed. 2009, 48(17), 3165-3169.
Sugars, Alkaloids, and Heteroaromatics: Exploring Heterocyclic Chemistry with Alkoxyallenes Malte Brasholz, Hans-Ulrich Reissig, and Reinhold Zimmer Acc. Chem. Res. 2009, 42(1), 45-56.
Scope of a Novel Three-Component Synthesis of Highly Functionalized Pyridines Jyotirmayee Dash, Tilman Lechel, and Hans-Ulrich Reissig Org. Lett. 2007 (26), 9, 5541-5544.
A New, Efficient and Stereoselective Synthesis of Tricyclic and Tetracyclic Compounds by Samarium Diiodide Induced Cyclisations of Naphthyl-Substituted Arylketones - An Easy Access to Steroid-Like Skeletons Francesca Aulenta, Mathias Berndt, Irene Brüdgam, Hans Hartl, Sebastian Sörgel, and Hans-Ulrich Reißig Chem. Eur. J. 2007, 13(21), 6047-6062.
