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 Publications 

  • M. Medvecký, I. Linder, L. Schefzig, H.-U. Reißig*, R. Zimmer*
    Iodination of Carbohydrate-Derived 1,2-Oxazines to Enantiopure 5-Iodo-3,6-dihydro-2H-1,2-oxazines and Subsequent Palladium-Catalyzed Cross-Coupling Reactions
    Beilstein J. Org. Chem. 2016, 12, 2898 – 2905.

  • R. Klemme, C. Bentz, T. Zukowski, L. Schefzig, D. Lentz, H.-U. Reißig,* R. Zimmer*
    Percarboxylic Acid Oxidation of α-Hydroxy-Substituted Alkoxy-allenes: The Unexpected Formation of Acyloxy-Substituted 1,2-Diketones and the Synthesis of Functionalized Quinoxalines
    Synthesis 2016, 48, 1491 – 1501.

  • M. Wilsdorf, H.-U. Reißig*
    Model Studies towards New Functionalized Bisbenzannulated [5,6]-Spiroketals
    Eur. J. Org. Chem. 2016, 1555–1561.

  • M. Jasiński*, G. Utecht, A. Fruziński, H.-U. Reißig
    Three-Step Synthesis of 3-Aminoseptanoside Derivatives Using Lithiated Methoxyallene and δ-Siloxynitrones
    Synthesis 2016, 48, 893 – 905.

  • J. Salta, J. Dernedde, H.-U. Reißig*
    Synthesis of Multivalent Carbohydrate Mimetics with Aminopolyol End Groups and their Evaluation as L-Selectin Inhibitors
    Beilstein J. Org. Chem. 2015, 11, 638 – 646.

  • J. Salta, H.-U. Reißig*
    Synthesis of Divalent Carbohydrate Mimetics by Reductive Amination with Enantiopure 1,2-Oxazines as Precursors
    Synthesis 2015, 47, 1893 – 1898.

  • R. Zimmer, H.-U. Reißig*
    Allenes in Multicomponent Synthesis of Heterocycles
    in: Multicomponent Reactions in Organic Synthesis, (J. Zhu, Q. Wang, M.-X. Wang, Eds.),
    WILEY-VCH, Weinheim 2015, 301 – 332.

  • M. Kandziora, E. Mucha, S. P. Zucker, H.-U.Reißig*
    Syntheses of Mono- and Divalent C-Aminoglycosides Using 1,2-Oxazine Chemistry and Olefin Metathesis
    Synlett 2015, 26, 367 – 374.

  • M. Kandziora, H.-U. Reißig*
    Preparation of Multivalent Carbohydrate Mimetics Based on Enantiopure 1,2-Oxazines by Sonogashira Coupling and Subsequent Reductive Ring-Opening
    Eur. J. Org. Chem. 2015, 370 – 377.

  • M. Jasiński, G. Mlostoń, M. Stolarski, W. Costa, M. Domínguez, H.-U. Reißig*
    Reactions of Cycloaliphatic Thioketones and Their Oxo Analogues with Lithiated Methoxyallene: A New Approach to Vinylthiiranes
    Chem. Asian J. 2014, 9, 2641 – 2648.

  • M. Kandziora, H.-U. Reißig*
    Synthesis of Rigid p-Terphenyl-Linked Carbohydrate Mimetics
    Beilstein J. Org. Chem. 2014, 10, 1749 – 1758.

  • R. Zimmer, H.-U. Reißig*
    Alkoxyallenes as Building Blocks for Organic Synthesis
    Chem. Soc. Rev. 2014, 43, 2888 – 2903.

  • M. K. Bera, M. Domínguez, P. Hommes, H.-U. Reißig*
    The Flögel-Three-Component Reaction with Dicarboxylic Acids - An Approach to Bis(β-alkoxy-β - ketoenamides) for the Synthesis of Complex Pyridine and Pyrimidine Derivatives
    Beilstein J. Org. Chem. 2014, 10, 394 – 404.

  • L. Bouché, M. Kandziora, H.-U. Reißig*
    Synthesis of new enantiopure poly(hydroxy)aminooxepanes as building blocks for multivalent carbohydrate mimetics
    Beilstein J. Org. Chem. 2014, 10, 213 – 223.

  • M. Jasiński, E. Moreno-Clavijo, H.-U. Reißig*
    Synthesis of a Series of Enantiopure Polyhydroxylated Bicyclic N-Heterocycles from an l-Erythrose Derived Nitrone and Alkoxyallenes
    Eur. J. Org. Chem. 2014, 442 – 454.

  • M. K. Bera, S. L. Gholap, P. Hommes, K. Neuthe, D. Trawny, J. P. Rabe, D. Lentz, R. Zimmer, H.-U. Reißig*
    Synthesis and Properties of Branched Oligo(2-thienyl)- and Oligo(2,2’-bithien-5-yl)-Substituted Pyridine Derivatives
    Adv. Synth. Catal. 2013, 355, 3463 – 3474.

  • V. M. Schmiedel, S. Stefani, H.-U. Reißig*
    Stereodivergent Synthesis of Jaspine B and its Isomers using a Carbohydrate-derived Alkoxyallene as C3-building Block
    Beilstein J. Org. Chem. 2013,9, 2564 – 2569.

  • C. Parmeggiani, F. Cardona, L. Giusti, H.-U. Reißig*, A. Goti
    Stereocomplementary Routes to Hydroxylated Nitrogen Heterocycles: Total Syntheses of Casuarine, Australine, and 7-epi-Australine
    Chem. Eur. J. 2013, 19, 10595 – 10604.
  • S. L. Gholap, P. Hommes, K. Neuthe, H.-U. Reißig*
    Per(2-thienyl)pyridines: Synthesis and Properties
    Org. Lett. 2013, 15, 318 – 321.

  • M. Jasiński,T. Watanabe, H.-U. Reißig*
    Samarium Diiodide Promoted Reduction of 3,6-Dihydro-2H-1,2-oxazines: Competition of 1,4-Amino Alcohol Formation and Ring Contraction to Pyrrole Derivatives
    Eur. J. Org. Chem. 2013, 605 – 610.

  • T. Lechel, G. Podolan, B. Brusilowskij, C. A. Schalley, H.-U. Reißig*
    Unexpected One-Step Formation of Iodo[1,3]dioxolo[4,5-c]pyridine Derivatives by a Hofmann-Löffler-Freytag Reaction: Studies on the Synthesis of a Pyridine-Containing Macrocycle
    Eur. J. Org. Chem. 2012, 5685 – 5692.

  • M. Jasiński, Dieter Lentz, E. Moreno-Clavijo, H.-U. Reißig*
    Application of L-Erythrose-Derived Nitrones in the Synthesis of Polyhydroxylated Compounds via 3,6-Dihydro-2H-1,2-oxazine Derivatives
    Eur. J. Org. Chem. 2012, 3304 – 3316.

  • M. Jasiński, Dieter Lentz, H.-U. Reißig*
    Carbohydrate-Auxiliary Assisted Preparation of Enantiopure 1,2-Oxazine Derivatives and Aminopolyols
    Beilstein J. Org. Chem. 2012, 8, 662-674.

  • L. Bouché, H.-U. Reißig*
    Synthesis of Novel Carbohydrate Mimetics via 1,2-Oxazines
    Pure Appl. Chem. 2012, 84, 23 – 36.

  • M. Roskamp, S. Enders, F. Pfrengle, S. Yekta. V. Dekaris, J. Dernedde, H.-U. Reißig, S. Schlecht*
    Multivalent Interaction and Selectivities in Selectin Binding of Functionalized Gold Colloids Decorated with Carbohydrate Mimetics
    Org. Biomol. Chem. 2011, 9, 7448 – 7456.

  • M. K. Bera, P. Hommes, H.-U. Reißig*
    In Search of Oligo(2-thienyl)-Substituted Pyridine Derivatives: A Modular Approach to Di-, Tri- and Tetra(2-thienyl)pyridines
    Chem. Eur. J. 2011, 17, 11838 – 11844.

  • C. Eidamshaus, R. Kumar, M. K. Bera, H.-U. Reißig*
    A Practical Two-Step Procedure for the Preparation of Enantiopure Pyridines: Multicomponent Reactions of Alkoxyallenes, Nitriles and Carboxylic Acids followed by a Cyclocondensation Reaction
    Beilstein J. Org. Chem. 2011, 7, 962   975.

  • T. Lechel, M. Gerhard, D. Trawny, B. Brusilowskij, L. Schefzig, R. Zimmer, J. P. Rabe, D. Lentz, C. A. Schalley, H.-U. Reißig*
    Synthesis of 5-Acetyloxazoles and 1,2-Diketones from β-Alkoxy-β-ketoenamides and Their Subsequent Transformations
    Chem.Eur. J. 2011, 17, 7480 – 7491.

  • V. Dekaris, R. Pulz, A. Al-Harrasi, D. Lentz, H.-U. Reißig*
    Stereoselective Synthesis of Aza, Amino and Imion Sugar Derivatives by Hydroboration of 3,6-Dihydro-2H-1,2-oxazines as Key Reaction
    Eur. J. Org. Chem. 2011, 3210 – 3219.

  • A. Al-Harrasi, L. Bouché, R. Zimmer, H.-U. Reißig*
    β-Alkoxy-γ-amino Aldehydes by Internal Redox Ring Cleavages of Carbohydrate-Derived Enantiopure 1,2-Oxazines and Preparation of Heterocycles with Aminopolyol Side Chain
    Synthesis 2011, 109 – 118.

  • M. Brasholz, B. Dugovič , H.-U. Reißig*
    3-Alkoxy-2,5-dihydrofurans by Gold-Catalyzed Allenyl Cyclizations and Their Transformation into 1,4-Dicarbonyl Compounds, Cyclopentenones, and Butenolides
    Synthesis 2010, 3855  –  3864.

  • F. Pfrengle, H.-U. Reißig*
    Internally Protected Amino Sugar Equivalents from Enantiopure 1,2-Oxazines: Synthesis of Variably Configured Carbohydrates with C-Branched Amino Sugar Units
    Chem. Eur. J. 2010, 16, 11915  –  11925.

  • T. Lechel, H.-U. Reißig*
    Synthesis of Heterocycles via Alkoxyallenes
    Pure Appl. Chem. 2010, 82, 1835 – 1844.

  • R. Zimmer, T. Lechel, G. Rancan, M. K. Bera, H.-U. Reißig*
    Preparation of Pyrimidine-N-oxides by Condensation of Functionalized Enamides with Hydroxylamine Hydrochloride
    Synlett 2010, 1793 – 1796.

  • M. K. Bera, H.-U. Reißig*
    A Route to Alkenyl-Substituted 4-Hydroxypyridine and Pyrimidine Derivatives via Three-Component Access to β-Alkoxy-β-ketoenamides
    Synthesis 2010, 2129 – 2138.

  • T. Lechel, J. Dash, C. Eidamshaus, I. Brüdgam, D. Lentz, H.-U. Reißig*
    A Three-component Synthesis of β-Alkoxy-β-keto-enamides - Flexible Precoursors for 4-Hydroxypyridine Derivatives and their Palladium-catalysed Reactions
    Org. Biomol. Chem. 2010, 8, 3007 – 3014.

  • T. Lechel, I. Brüdgam, H.-U. Reißig*
    Preparation of pyridine-3,4-diols, their crystal packing and their use as precursors for palladium-catalyzed cross-coupling reactions
    Beilstein Journal of Organic Chemistry 2010, 6, No. 42.

  • T. Lechel, H.-U. Reißig*
    New 5-Alkoxypyrimidine Derivatives from β-Alkoxy β-Keto Enamides and Ammonium Salts
    Eur. J. Org. Chem. 2010, 2555 – 2564.

  • T. Lechel, J. Dash, P. Hommes, D. Lentz, H.-U. Reißig*
    Three-Component Synthesis of Perfluoroalkyl- or Perfluoroaryl-Substituted 4-Hydroxypyridine Derivatives and Their Palladium-Catalyzed Coupling Reactions
    J. Org. Chem. 2010, 75, 726 – 732.

  • F. Pfrengle, H.-U. Reißig*
    Amino Sugars and their Mimetics via 1,2-Oxazines
    Chem. Soc. Rev., 2010, 39, 549 – 557.

  • E. Moreno-Clavijo, A. T. Carmona, H.-U. Reißig, A. J. Moreno-Vargas, E. Alvarez, I. Robina*
    Allenyl Sulfones and Allenyl Sulfides in the Synthesis of 3-Pyrrolines. A Novel Nucleophilic [3 + 2] Cycloaddition on Allenyl Sulfones Giving Rearranged Cycloadducts
    Org. Lett. 2009, 11, 4778 – 4781.

  • A. Al-Harrasi, S. Fischer, R. Zimmer, H.-U. Reißig*
    Ring Enlargement of Carbohydrate-Derived 1,2-Oxazines to Enantiopure 5-Bromo-1,2-oxazepines and Subsequent Palladium-Catalyzed Reactions
    Synthesis 2010, 304 – 314.

  • V. Dekaris, B. Bressel, H.-U. Reißig*
    Acid Mediated Transformations of Enantiopure 3,6-Dihydro-2H-1,2-oxazines into Functionalized Aminotetrahydrofuran Derivatives
    Synlett 2010, 47 – 50.

  • V. Dekaris, H.-U. Reißig*
    Stereocontrolled Syntheses of Enantiopure Polyhydroxylated Azetidines via 1,2-Oxazines
    Synlett 2010, 42 – 46.

  • A. Al-Harrasi, F. Pfrengle, V. Prisyazhnyuk, S. Yekta, P. Koóš, H.-U. Reißig*
    Enantiopure Aminopyrans by a Lewis Acid Promoted Rearrangement of 1,2-Oxazines: Versatile Building Blocks for Oligosaccharide and Sugar Amino Acid Mimetics
    Chem. Eur. J. 2009, 15, 11632  –  11642

  • V. Prisyazhnyuk, M. Jachan, I. Brüdgam, R. Zimmer, H.-U. Reißig*
    Addition of Lithiated Methoxyallene to Aziridines – A Novel Access to Enantiopure Piperidine and β-Amino Acid Derivatives
    Collect. Czech. Chem. Commun, 2009, 74, 1069 – 1080.

  • M. Brasholz, H.-U. Reißig*
    Alkoxyallene-Based De Novo Synthesis of Rare Deoxy Sugars: New Routes to L-Cymarose, L-Sarmentose, L-Diginose and L-Oleandrose
    Eur. J. Org. Chem. 2009, 3595– 3604.

  • T. Lechel, D. Lentz, H.-U. Reißig*
    Three-Component Synthesis of Highly Functionalized 5-Acetyloxazoles
    Chem. Eur. J. 2009, 15, 5432  –  5435.

  • C. Eidamshaus, H.-U. Reißig*
    Hihgly Funtionalized Enantiopure 4-Hydroxypyridine Derivatives by a Versatile Three-Component Synthesis
    Adv. Synth. Catal. 2009, 351, 1162 - 1166.

  • F. Pfrengle, D. Lentz, H.-U. Reißig*
    Stereodivergente De-novo-Synthese verzweigter Aminozucker durch Lewis-Säure-induzierte Umlagerung von 1,2-Oxazinen
    Angew. Chem. 2009, 121, 3211 - 3215.

  • F. Pfrengle, D. Lentz, H.-U. Reißig*
    Stereodivergent De novo Synthesis of Branched Amino Sugars by Lewis Acid promoted Rearrangement of 1,2-Oxazines
    Angew. Chem. Int. Ed. 2009, 48, 3165 - 3169.

  • T. Lechel, S. Möhl, H.-U. Reißig*
    A Concise Synthesis of Alkoxy-Substituted Pyrimidine Derivatives Based upon a Three-Component Access to Functionalized Enamides
    Synlett 2009, 1059 1062.

  • B. Bressel, H.-U. Reißig*
    A New Approach to Neuraminic Acid Analogues via 1,2-Oxazines
    Org. Lett. 2009, 11, 527 – 530.

  • M. Brasholz, H.-U. Reißig,* R. Zimmer
    Sugars, Alkaloids and Heteroaromatics: Exploring Heterocyclic Chemistry with Alkoxyallenes
    Acc. Chem. Res. 2009, 42, 45 – 56.

  • F. Pfrengle, A. Al-Harrasi, I. Brüdgam, H.-U. Reißig*
    Unusual Enantiopure Heterocyclic Skeletons via Lewis Acid Promoted Rearrangements of 1,3-Dioxolanyl-Substituted 1,2-Oxazines
    Eur. J. Org. Chem. 2009, 282 – 291.

  • F. Pfrengle, V. Dekaris, L. Schefzig, R. Zimmer, H.-U. Reißig*
    Indium Trichloride Mediated Cleavage of Acetonides in the Presence of Acid-Labile Functional Groups – Enhancing the Synthetic Utility of 1,3-Dioxolanyl-Substituted 1,2-Oxazines
    Synlett 2008, 2965– 2968.

  • J. Dash, I. Brüdgam, H. Hartl, H.-U. Reißig*
    Crystal structure of 1,4-bis[3-methoxy-4(4-methoxyphenyl)-6-(trifluoromethyl)-pyridin-2-yl]benzene, C34H26F6N2O4Z.
    Kristallogr. NCS
    2008, 223, 347.

  • R. Zimmer, M. Taszarek. L. Schefzig, H.-U. Reißig*
    Reaction of a Polycyclic Diketone with Lithiated Methoxyallene: Synthesis of New Functionalized Cage Compounds
    Synlett, 2008, 2046 – 2050.

  • T. Lechel, J. Dash, I. Brüdgam, H.-U. Reißig*
    Novel Furopyridine Derivatives via Sonogashira Reactions of Functionalized Pyridines
    Eur. J. Org. Chem. 2008, 3647– 3655.

  • B. Dugovič, H.-U. Reißig*
    A New Alkoxyallene-Based [3+2] Approach to the Synthesis of Highly Substituted Cyclopentenones
    Synlett 2008, 769 – 773.

  • M. Gwiazda, H.-U. Reißig*
    Highly Substituted Imidazole Derivatives from a New Four-Component Synthesis Employing Methoxyallene
    Synthesis 2008, 990 – 994.

  • B. Bressel, B. Egart, A. Al-Harrasi, R. Pulz, H.-U. Reißig,* I. Brüdgam
    Acid-Induced and Reductive Transformations of Enantiopure 3,6-Dihydro-2H-1,2-oxazines – Synthesis of Dideoxyamino Carbohydrate Derivatives
    Eur. J. Org. Chem. 2008, 467 – 474.

  • B. Dugovič, L. Fišera, H.-U. Reißig*
    1,3-Dipolar Cycloadditions of N-Benzyl-2,3-O-isopropylidene-D-glyceraldehyde Nitrone to Methoxyallene – Control of Site- and Diastereoselectivity of Isoxazolidine Formation by Lewis Acids
    Eur. J. Org. Chem. 2008, 277 – 284.

  • S. Yekta, V. Prisyazhnyuk, H.-U. Reißig*
    Simple Modifications of Enantiopure 1,2-Oxazines Leading to Building Blocks for Carbohydrate and Peptide Mimetics
    Synlett 2007, 2069 – 2072.

  • M. Brasholz, H.-U. Reißig*
    Refined Protocols for the Preparation of 3-Alkoxy-2,5-dihydrofurans, Allylic Oxidation to β-Alkoxybutenolides and Short Synthesis of (±)-Annularin H
    Synlett 2007, 1294 - 1298.

  • M. Brasholz, H.-U. Reißig*
    Oxidative Spaltung von 3-Alkoxy-2,5-dihydrofuranen und ihre Anwendung in der
    De-novo-Synthese seltener Monosaccharide am Beispiel von L-Cymarose

    Angew. Chem. 2007, 119, 1659  –  1662; Angew. Chem. Int. Ed. 2007, 46, 1634 - 1637.

  • F. Pfrengle, A. Al-Harrasi, H.-U. Reißig*
    Lewis Acid Promoted Rearrangements of 1,3-Dioxolanyl-Substituted 1,2-Oxazines
    into Novel Products with 1,3,6-Trioxa-7-azacyclopenta[cd]indene Skeletons

    Synlett 2006, 3498 – 3500.

  • S. Sörgel, C. Azap, H.-U. Reißig*
    Synthesis of Bisbenzannulated Spiroketals - Model Studies for a Modular Approach
    to Rubromycins

    Org. Lett. 2006, 8, 4875 - 4878.
     
  • S. Kaden, H.-U. Reißig*
    Efficient Approach to the Azaspirane Core of FR 901483
    Org. Lett. 2006, 8, 4763 - 4766.

  • S. Sörgel, C. Azap, H.-U. Reißig*
    Preparation of Highly Alkoxy-Substituted Naphthaldehyde Derivatives - A
    Regioselective Approach to Building  Blocks for the Synthesis of Rubromycins

    Eur. J. Org. Chem. 2006, 4405 - 4418.
     
  • M. A. Chowdhury, H.-U. Reißig*
    Syntheses of Highly Substituted Furan and Pyrrole Derivatives via
    Lithiated 3-Aryl-1-methoxyallenes:  Application to the Synthesis of Codonopsinine

    Synlett 2006, 2383 - 2386.
     
  • M. Gwiazda, H.-U. Reißig*
    A Four-Component Synthesis of Highly Substituted Imidazole Derivatives
    Synlett 2006, 1683 - 1686.
     
  • M. A. Chowdhury, I. Brüdgam, H. Hartl, H.-U. Reißig*
    Crystal structure of (3R,6S,4'S-2-benzyl-3-(2',2'-dimethyl[1',3']dioxolan-
    4'-yl)-4-methoxy-6-phenyl-3,6- dihydro-2H-1,2-oxazine, C23H27NO4

    Z. Kristallogr. NCS 2006, 221, 213 - 214.
     
  • A. Al-Harrasi, I. Brüdgam, H. Hartl, H.-U. Reißig*
    Crystal structure of 3S,4S,5R,6S,7R-5-amino-6-(tert-butyldimetylsiloxy)-
    7(tert-butyldimetyl-siloxymethyl)-3-hydroxymethyl-2,2-dimethyloxepan-
    4-ol, C22H49NO5Si2

    Z. Kristallogr. NCS 2006, 221, 131 - 132.

  • S. Kaden, H.-U. Reißig*, I. Brüdgam, H. Hartl
    Additions of Lithiated Alkoxyallenes to Phthalimide: A New Synthesis of
    Pyrroloisoindolones and an Unusual Olefination Reaction

    Synthesis 2006, 1351 - 1359.

  • A. Al-Harrasi, I. Brüdgam, H. Hartl, H.-U. Reißig*
    Crystal Structure of 3S,4'S,6'S-2-benzyl-3-[(tert-butyldimetylsiloxy)- 2',2'-dimethyl-1,3-dioxolan-4'-yl)-6'-methyl]-4[2-[(trimethylsilyl)ethoxy]- 3,6-dihydro-2H-1,2-oxazine, C28H49NO5Si2
    Z. Kristallogr. NCS 2006, 221, 12 - 14.

  • Patent:
    O. Flögel, H.-U. Reißig
    Substituierte Pyridine
    Deutsches Patentamt (DE 10336497 vom 03.03.2005).
     
  • R. Zimmer*, H.-U. Reißig
    1-Methoxyallenyllithium
    in: Electronic Encyclopedia of Reagents for Organic Synthesis
    John Wiley & Sons, Chichester, 2005.

  •  A. Al-Harrasi, I. Brüdgam, H. Hartl, H.-U. Reißig*
    Crystal structure of 1R,5S,8R,9S-8-azidomethyl-2-benzyl-6,6-dimethyl-3,7-dioxa-
    2-azabicyclo[3.3.1]nonan-9-ol, C16H22N4O3
    Z. Kristallogr. NCS 2005, 220, 599  –  600.

  • A. Al-Harrasi, H.-U. Reißig*
    Enantiomerenreine Kohlenhydratmimetika durch Lewis-Säure-induzierte Umlagerung von 1,3-dioxolanylsubstitutierten 1,2-Oxazinen
    Angew. Chem. 2005, 117, 6383  –  6387.

  • A. Al-Harrasi, H.-U. Reißig*
    Ring Enlargement of 1,2-Oxazines to Enantiopure 1,2-Oxazepine Derivatives
    and their Palladium-Catalyzed Couplings

    Synlett 2005, 2376 - 2378.

  • S. Kaden, M. Brockmann, H.-U. Reißig*
    Synthesis of Enantiopure 2-Substituted Pyrrolidin-3-ones via Lithiated
    Alkoxyallenes - An Auxilary Based Synthesis of Both Enantiomers of the Antibiotic Anisomycin.

    Helv. Chim. Acta 2005, 88, 1826 - 1838.
     
  • A. Al-Harrasi, H.-U. Reißig*
    Synthesis of Enantiopure Functionalized β-Alkoxy γ -Amino  Aldehydes by a New Internal Redox Ring Cleavage of Carbohydrate Derived 1,2-Oxazines
    Synlett 2005, 1152 - 1154.
     
  • M. Helms, W. Schade, R. Pulz, T. Watanabe, A. Al-Harrasi, L. Fisera,
    I. Hlobilová, G. Zahn, H.-U. Reißig*
    Stereodivergent Syntheses of Highly Substituted Enantiopure
    4-Alkoxy-3,6-dihydro-2H-1,2-oxazines by Addition of Lithiated Alkoxyallenes to Carbohydrate-Derived Aldonitrones

    Eur. J. Org. Chem. 2005, 1003 - 1019.
     
  • M. Helms, H.-U. Reißig*
    Ozonolyses of Enantiopure 4-Alkoxy-3,6-dihydro-2H-1,2-oxazines: An Expedient Route to Functionalized-Amino-β-hydroxy Esters
    Eur. J. Org. Chem. 2005, 998-1001.

  • C. Azap, P. Luger*, H.-U. Reißig, A. Wagner
    Crystal Structure of 4,7,8-Trimethoxy-3-hydroxyspiro[1-benzofuran-2,2'-
    chromane] chloroform disolvate, C19H20O6 · 2 CHCl3

    Z. Kristallogr. NCS 2004, 219, 495 - 496.
     
  • C. Azap, P. Luger*, H.-U. Reißig, A. Wagner
    Crystal Structure of 4,7-Dimethoxy-3-hydroxyspiro[1-benzofuran-2,2'-chromane] chloroform solvate
    (1 : 1/3), C18H18O5 · 1/3 CHCl3

    Z. Kristallogr. NCS 2004, 219, 492 - 494.

  • R. Zimmer, H.-U. Reißig
    Donor-Substituted Allenes
    in "Modern Allene Chemistry" (N. Krause, A. S. K. Hashmi, Eds.), S. 425 – 492, WILEY-VCH, Weinheim 2004.  

  • O. Flögel, J. Dash, I. Brüdgam, H. Hartl, H.-U. Reißig*
    A New Color of the Synthetic Chameleon Methoxyallene:  Synthesis of Trifluoromethyl-Substituted Pyridinol Derivatives - An Unusual Reaction Mechanism, a Remarkable Crystal Packing, and First Palladium-Catalyzed Coupling Reactions
    Chem. Eur. J. 2004, 10, 4283 - 4290.

  • O. Flögel, H.-U. Reißig*
    Direct Synthesis of Functionalized Pyrrole Derivatives from  Aldehydes, Bis(trimethylsilyl)amide and  Methoxyallene
    Synlett 2004, 895 - 897.

  • O. Flögel, H.-U. Reißig*
    Preparation of α,β-Unsaturated γ-Keto Aldehydes and New  Tetronic Acid and Pyridazine Derivatives by Oxidative Transformations of Alkoxyallene-Based Dihydrofurans
    Eur. J. Org. Chem. 2004, 2797 - 2804.

  • O. Flögel, M. G. Okala Amombo, H.-U. Reißig*, G. Zahn, I. Brüdgam, H. Hartl
    A Stereoselective and Short Total Synthesis of the Polyhydroxylated
    γ-Amino Acid (–)-Detoxinine Based on Stereoselective Preparation of Dihydropyrrole Derivatives from  Lithiated Alkoxyallenes

    Chem. Eur. J. 2003, 9, 1405 - 1415.
     
  • R. Pulz, S. Cicchi, A. Brandi, H.-U. Reißig*
    Synthesis of New Enantiopure Bicyclic 1,2-Oxazines by Addition of  Lithiated Methoxyallene to Chiral Cyclic Nitrones
    Eur. J. Org. Chem. 2003, 1153 - 1156.

  • R. Pulz, W. Schade, H.-U. Reißig*
    Synthesis of Enantiopure Amino Polyols and Pyrrolidine Derivatives from  5-Bromo-1,2-oxazin-4-ones
    Synlett 2003, 405 - 407.

  • R. Pulz, A. Al-Harrasi, H.-U. Reißig*
    New Polyhydroxylated Pyrrolidines Derived from Enantiopure 3,6-
    Dihydro-2H-1,2-oxazines

    Org. Lett. 2002, 4, 2353 - 2355.

  • R. Pulz, A. Al-Harrasi, H.-U. Reißig*
    Acid Promoted Syntheses of New Enatiopure Amino Sugar Derivatives from 3,6-Dihydro-2H-1,2-oxazines
    Synlett 2002, 817 - 819.

  • H.-U. Reißig*, W. Schade, M. G. Okala Amombo, R. Pulz, A. Hausherr
    Stereoselective Syntheses of Heterocycles via Metallated Alkoxyallenes
    Pure Appl. Chem. 2002, 74, 175 - 180.

  • A. Hausherr, B. Orschel, S. Scherer, H.-U. Reißig*
    Synthesis of Enantiopure 1-Alkoxyallenes and their 3-Alkylated Derivatives
    Synthesis 2001, 1377 - 1385.

  • R. Pulz, T. Watanabe, W. Schade, H.-U. Reißig*
    A Stereodivergent Synthesis of Enantiopure 3-Methoxypyrrolidines and
    3-Methoxy-2,5-dihydropyrroles from 3,6-Dihydro-2H-1,2-oxazines

    Synlett 2000, 983 - 986.
     
  • H.-U. Reißig*, S. Hormuth, W. Schade, M. Okala Amombo, T. Watanabe, R. Pulz, A. Hausherr,
    R. Zimmer
    Stereoselective Syntheses of Heterocycles with Lithiated Methoxyallene
    Lectures in Heterocyclic Chemistry Vol XVI in J. Heterocycl. Chem. 2000, 37, 597 - 606.
     
  • H.-U. Reißig
    Lithiiertes Methoxyallen - ein unglaublich vielseitiger Baustein
    GIT Labor-Fachzeitschrift 2000, 44, 254 - 256.

  • R. Pulz, W. Schade, H.-U. Reißig, O. Rademacher*
    Crystal Structure of (3R, 5R, 4'S)-2-Benzyl-5-bromo-3-(2',2'-dimethyl-
    1',3'-dioxolan-4'-yl)3,4,5,6-tetrahydro-2H-1,2-oxazin-4-one, C16H20BrNO4

    Z. Kristallogr. NCS 2000, 215, 73 - 74.
     
  • M. Okala Amombo, A. Hausherr, H.-U. Reißig*
    An Expedient Synthesis of Pyrrole Derivatives by Reaction of Lithiated Methoxyallenes with Imines
    Synlett 1999, 1871 - 1874.

  • W. Schade, H.-U. Reißig*
    Stereocontrolled Synthesis of the Taxol C-13 Side Chain: Methyl- (2R,3S)-
    3-Benzoylamino-2-hydroxy-3-phenylpropanoate

    J. Prakt. Chem. 1999, 341, 685 - 686.
     
  • W. Schade, H.-U. Reißig*
    A New Diastereoselective Synthesis of Enantiomerically Pure 1,2-Oxazine Derivatives by Addition of  Lithiated Methoxyallene to Chiral Nitrones
    Synlett 1999, 632 - 634.
     
  • W. Schade, H.-U. Reißig, G. Zahn*
    Crystal Structure of (5S,9S,13S,14S,1'S)-14-[1-(N,N-Dibenzylamino)ethyl]-
    1,8,12,15-tetraoxatrispiro[4.3.3.4]heptadecan-4-one, C29H35NO5

    Z. Kristallogr. 1997, 212, 73 - 74.

  • S. Hormuth, W. Schade, H.-U. Reißig*
    First Synthesis of Enantiomerically Pure Primary Helical Spirocycles Based on the Repetitive Addition of Lithiated Methoxyallene to Chiral 3(2H)-Dihydrofuranone Derivatives
    Liebigs Ann. 1996, 2001 - 2006.
     
  • S. Hormuth, H.-U. Reißig*, D. Dorsch
    Stereoselective Synthesis of (2R,3S)-Norstatine Derivatives by Addition of Lithiated Methoxyallene to Amino Aldehydes and Subsequent Ozonolysis
    Liebigs Ann. Chem. 1994, 121 - 127.

  • S. Hormuth, H.-U. Reißig*
    Stereoselective Synthesis of 3(2H)-Dihydrofuranones by Addition of Lithiated Methoxyallene to Chiral Aldehydes
    J. Org. Chem. 1994, 59, 67 - 73.
     
  • S. Hormuth, H.-U. Reißig, S. Foro, H. J. Lindner*
    Crystal Structure of (2S,1'S)-2-[1-(N,N-Dibenzylamino)ethyl]-3(2H)-4,5-
    dihydrofuranone, OCH2CH2COCHCH(CH3)NCH2(C6H5)CH2(C6H5)

    Z. Kristallogr. 1993, 208, 157 - 160.

  • S. Hormuth, H.-U. Reißig, S. Foro, H. J. Lindner*
    Crystal Structure of (5R,1'S)-5-[1-(N,N-Dibenzylamino)ethyl]-2(3H)-4,5-
    dihydrofuranone, CH(CH2)2COOCHCH3NCH2(C6H5)CH2(C6H5)

    Z. Kristallogr. 1993, 208, 154 - 156.

  • S. Hormuth, H.-U. Reißig*, D. Dorsch*
    Titaniertes Methoxyallen als neuartiges Homoaldoläquivalent in diastereoselektiven Additionen an chirale Aminoaldehyde
    Angew. Chem. 1993, 105, 1513 - 1514.

  • S. Hormuth, H.-U. Reißig*, D. Dorsch*
    Titanated Methoxyallene as Novel Homoaldol Equivalent for Diastereoselective Additions to Chiral Amino Aldehydes
    Angew. Chem. Int. Ed. Engl. 1993, 32, 1449 – 1450.

  • S. Hormuth, H.-U. Reißig*
    Diastereoselective Additions of Lithiated Methoxyallene towards Chiral Aldehydes
    Synlett 1991, 179 - 180.
Direct link

Synthesis of Natural Products and Analogues

Publications

•  M. Wilsdorf*, S. Sörgel, H.-U. Reißig*
Lessons Learned During Spiroketalization Experiments – Progress and Setbacks in the Preparation of Oxygenated Rubromycins and Synthesis of 3´-Desoxyheliquino-mycinone
Eur. J. Org. Chem. 2016, 5757 – 5769.

•  M. Wilsdorf*, H.-U. Reißig*
Towards γ-Rubromycin: Model Studies, Development of a New C3 Building Block and Synthesis of 4´-Silyl-γ-rubromycin
Eur. J. Org. Chem. 2016, 5747 – 5756.

M. Wilsdorf, H.-U. Reißig*
Model Studies towards New Functionalized Bisbenzannulated [5,6]-Spiroketals
Eur. J. Org. Chem. 2016, 1555–1561.

M. Jasiński*, G. Utecht, A. Fruziński, H.-U. Reißig
Three-Step Synthesis of 3-Aminoseptanoside Derivatives Using Lithiated Methoxyallene and δ-Siloxynitrones
Synthesis 2016, 48, 893 – 905.

•  H. R. A. Golf, A. M. Oltmanns, D. H. Trieu, H.-U. Reissig,* A. Wiehe*
Synthesis of Functionalized BODIPYs, BODIPY-Corrole, and BODIPY-Porphyrin Arrays with 1,2,3-Triazole Linkers Using the 4-Azido(tetrafluorophenyl)-BODIPY Building Block
Eur. J. Org. Chem. 2015, 4224 – 4237.

•  C. Beemelmanns, H.-U. Reissig*
Strychnine as Target, Samarium Diiodide as Tool: A Personal Story
Chem. Rec. 2015, 15, 872 – 885.

H. R. A. Golf, H.-U. Reissig*, A. Wiehe*
Synthesis of SF5-Substituted Tetrapyrroles, Metalloporphyrins, BODIPYs, and Their Dipyrrane Precursors
J. Org. Chem. 2015, 80, 5133 – 5143.

C. Beemelmanns, H.-U. Reissig*
Evolution of a Short Route to Strychnine by Using the Samarium-Diiodide-Induced Cascade Cyclization as a Key Step
Chem. Eur. J. 2015, 21, 8416 – 8425.

H. R. A. Golf, H.-U. Reißig*, A. Wiehe*
Nucleophilic Substitution on (Pentafluorophenyl)dipyrromethane: A New Route to Building Blocks for Functionalized BODIPYs and Tetrapyrroles
Org. Lett. 2015, 17, 982 – 985.

H. R. A. Golf, H.-U. Reißig, A. Wiehe*
Regioselective Nucleophilic Aromatic Substitution Reaction of meso-Pentafluorophenyl-Substituted Porphyrinoids with Alcohols
Eur. J. Org. Chem. 2015, 1548 – 1568.

C. N. Rao, D. Lentz, H.-U. Reißig*
Synthese polycyclischer tertiärer Carbinamine durch Samariumdiiodid-vermittelte Cyclisierungen von Indolylsulfinylimien
Angew. Chem. 2015, 127, 2788 – 2792.

C. N. Rao, D. Lentz, H.-U. Reißig*
Synthesis of Polycyclic Tertiary Carbinamines by Samarium Diiodide Mediated Cyclizations of Indolyl Sulfinyl Imines
Angew. Chem. Int. Ed. 2015, 54, 2750 – 2753.

M. Wilsdorf, H.-U. Reißig*
Eine konvergente Totalsynthese des Telomerase-Inhibitors (±)-γ-Rubromycin
Angew. Chem. 2014, 126, 4420 – 4424.

M. Wilsdorf, H.-U. Reißig*
A Convergent Total Synthesis of the Telomerase Inhibitor (±)-γ-Rubromycin
Angew. Chem. Int. Ed. 2014, 53, 4332 – 4336.

 M. Jasiński, E. Moreno-Clavijo, H.-U. Reißig*
Synthesis of a Series of Enantiopure Polyhydroxylated Bicyclic N-Heterocycles from an l-Erythrose Derived Nitrone and Alkoxyallenes
Eur. J. Org. Chem. 2014, 442 – 454.

 C. Beemelmanns, S. Gross, H.-U. Reißig*
Towards the Core Structure of Strychnos Alkaloids Using Samarium Diiodide-Induced Reactions of Indole Derivatives
Chem. Eur. J. 2013,19, 17801 – 17808.

V. M. Schmiedel, S. Stefani, H.-U. Reißig*

Stereodivergent Synthesis of Jaspine B and its Isomers using a Carbohydrate-derived Alkoxyallene as C3-building Block
Beilstein J. Org. Chem. 2013,9, 2564 – 2569.

T. H. Ngo, H. Berndt, M. Wilsdorf, D. Lentz, H.-U. Reißig*

Linear and Cyclic Hybrids of Alternating Thiophene–Amino Acid Units: Synthesis and Effects of Chirality on Conformation and Molecular Packing
Chem. Eur. J. 2013,19, 15155 – 15165.

 

C. Parmeggiani, F. Cardona, L. Giusti, H.-U. Reißig*, A. Goti
Stereocomplementary Routes to Hydroxylated Nitrogen Heterocycles: Total Syntheses of Casuarine, Australine, and 7-epi-Australine
Chem. Eur. J. 2013, 19, 10595 – 10604.

 

M. H. Beyzavi, C. Nietzold, H.-U. Reißig*, A. Wiehe*
Synthesis of Functionalized trans-A2B2-Porphyrins Using Donor-Acceptor Cyclopropane-Derived Dipyrromethanes
Adv. Synth. Catal. 2013, 355, 1409 – 1422.

M. Wilsdorf, D. Leichnitz, H.-U. Reißig*
Trifluoromethanesulfonic Acid Catalyzed Friedel-Crafts Alkylations of 1,2,4-Trimethoxybenzene with Aldehydes or Benzylic Alcohols
Org. Lett. 2013, 15, 2494 – 2497.

M. H. Beyzavi, D. Lentz, H.-U. Reißig*, A. Wiehe*
Synthesis of New Functionalized Calix[n]phyrin Macrocycles with Varied Ring Sizes by Using a Sterically Congested Dipyrromethane
Chem. Eur. J. 2013, 19, 6203 – 6208.

T. H. Ngo, H. Berndt, D. Lentz, H.-U. Reißig*
Linear and Cyclic Amides with a Thiophene Backbone: Ultrasound-Promoted Synthesis and Crystal Structures
J. Org. Chem. 2012, 77, 9676 – 9683.

M. Wilsdorf, H.-U. Reißig*
Einfach und dennoch herausfordernd: Neues zur asymmetrischen Synthese von Spiroketalen
Angew. Chem. 2012, 124, 9624  –  9626.

M. Wilsdorf, H.-U. Reißig*
Simple, but Challenging: Recent Developments in the Asymmetric Synthesis of Spiroketals
Angew. Chem. Int. Ed. 2012, 51, 9486  –  9488.

M. Jasiński, Dieter Lentz, E. Moreno-Clavijo, H.-U. Reißig*
Application of L-Erythrose-Derived Nitrones in the Synthesis of Polyhydroxylated Compounds via 3,6-Dihydro-2H-1,2-oxazine Derivatives
Eur. J. Org. Chem. 2012, 3304 – 3316.

M. Jasiński, Dieter Lentz, H.-U. Reißig*
Carbohydrate-Auxiliary Assisted Preparation of Enantiopure 1,2-Oxazine Derivatives and Aminopolyols
Beilstein J. Org. Chem. 2012, 8, 662-674.

L. Bouché, H.-U. Reißig*
Synthesis of Novel Carbohydrate Mimetics via 1,2-Oxazines
Pure Appl. Chem. 2012, 84, 23 – 36.

•  C. Beemelmanns, D. Lentz, H.-U. Reißig*
Samarium Diiodide Induced Cyclizations of γ-, δ- and ε-Indolyl Ketones: Reductive Coupling, Intermolecular Trapping, and Subsequent Transformations of Indolines
Chem. Eur. J. 2011, 17, 9720 9730.

•  V. Dekaris, R. Pulz, A. Al-Harrasi, D. Lentz, H.-U. Reißig*
Stereoselective Synthesis of Aza, Amino and Imion Sugar Derivatives by Hydroboration of 3,6-Dihydro-2H-1,2-oxazines as Key Reaction
Eur. J. Org. Chem. 2011, 3210 – 3219.

C. Beemelmanns, H.-U. Reißig*
Samarium diiodide induced ketyl-(het)arene cyclisations towards novel N-heterocycles
Chem. Soc. Rev., 2011, 40, 2199 – 2210.

H. Özbek, D. Lentz, H.-U. Reißig*
New Macrocyclic Peptidomimetics Containing 5-Aminothiophene Subunits
Eur. J. Org. Chem. 2010, 6319 – 6322.

M. Brasholz, B. Dugovič , H.-U. Reißig*
3-Alkoxy-2,5-dihydrofurans by Gold-Catalyzed Allenyl Cyclizations and Their Transformation into 1,4-Dicarbonyl Compounds, Cyclopentenones, and Butenolides
Synthesis 2010, 3855  –  3864.

•  C. Beemelmanns, H.-U. Reißig*
Eine kurze formale Strychnin-Totalsynthese mit einer Samariumdiiodid-induzierten Kaskadenreaktion als Schlüsselschritt
Angew. Chem. 2010, 122, 8195  –  8199.

C. Beemelmanns, H.-U. Reißig*
A Short Formal Total Synthesis of Strychnine with a Samarium Diiodide Induced Cascade Reaction as the Key Step
Angew. Chem. Int. Ed. 2010, 49, 8021  –  8025.

F. Pfrengle, H.-U. Reißig*
Internally Protected Amino Sugar Equivalents from Enantiopure 1,2-Oxazines: Synthesis of Variably Configured Carbohydrates with C-Branched Amino Sugar Units
Chem. Eur. J. 2010, 16, 11915  –  11925.

•  A. Schwanke, C. Murruzzu, B. Zdrazil. R. Zuhse, M. Natek, M. Höltje, H. C. Korting, H.-U. Reißig, H.-D. Höltje, M. Schäfer-Korting*
Antitumor Effects of Guanosine-Analog Phosphonates Identified by Molecular Modelling
Int. J. Pharm. 2010, 397, 9 – 18.

U. K. Wefelscheid, H.-U. Reißig*
Synthesis of New Steroid Analogues by Samarium Diiodide Induced Cyclisations of γ-Naphthyl 1,3-Diones
Tetrahedron: Asymmetry 2010, 21, 1601 – 1610.

F. Pfrengle, H.-U. Reißig*
Addition of Lithiated Enol Ethers to Nitrones and Subsequent Lewis Acid Induced Cyclizations to Enantiopure 3,6-Dihydro-2H-pyrans – an Approach to Carbohydrate Mimetics
Beilstein Journal of Organic Chemistry 2010, 6, No. 75.

M. Höltje, A. Richartz, B. Zdrazil, A. Schwanke, B. Dugovič, C. Murruzzu, H.-U. Reißig, H. C. Korting, B. Kleuser, H.-D. Höltje, M. Schäfer-Korting*
Human Polymerase α-Inhibitors for Skin Tumors. Part 2. Modeling, Synthesis and Influence on Normal and Transformed Keratinocytes of New Thymidine and Purine Derivatives
J. Enzym. Inhib. Med. Chem., 2010, 25 (2), 250-265.

V. Dekaris, H.-U. Reißig*
Stereocontrolled Syntheses of Enantiopure Polyhydroxylated Azetidines via 1,2-Oxazines
Synlett 2010, 42 – 46.

F. Pfrengle, D. Lentz, H.-U. Reißig*
A New Ring Closure Approach to Enantiopure 3,6-Dihydro-2H-pyrans: Stereodivergent Access to Carbohydrate Mimetics
Org. Lett. 2009, 11, 5534 – 5537.

V. Prisyazhnyuk, M. Jachan, I. Brüdgam, R. Zimmer, H.-U. Reißig*
Addition of Lithiated Methoxyallene to Aziridines – A Novel Access to Enantiopure Piperidine and β-Amino Acid Derivatives
Collect. Czech. Chem. Commun, 2009, 74, 1069 – 1080.

M. Brasholz, H.-U. Reißig*
Alkoxyallene-Based De Novo Synthesis of Rare Deoxy Sugars: New Routes to L-Cymarose, L-Sarmentose, L-Diginose and L-Oleandrose
Eur. J. Org. Chem. 2009, 3595– 3604.

J. Dash, H.-U. Reißig*
A New and Flexible Synthesis of 4-Hydroxypyridines: Rapid Access to Caerulomycins A, E and Functionalized Terpyridines
Chem. Eur. J. 2009, 15, 6811  –  6814.

F. Pfrengle, D. Lentz, H.-U. Reißig*
Stereodivergente De-novo-Synthese verzweigter Aminozucker durch Lewis-Säure-induzierte Umlagerung von 1,2-Oxazinen
Angew. Chem. 2009, 121, 3211 - 3215.

  F. Pfrengle, D. Lentz, H.-U. Reißig*
Stereodivergent De novo Synthesis of Branched Amino Sugars by Lewis Acid promoted Rearrangement of 1,2-Oxazines
Angew. Chem. Int. Ed. 2009, 48, 3165 - 3169.

V. Blot, U. Jacquemard, H.-U. Reißig,* B. Kleuser
Practical Syntheses of Sphingosine-1-Phosphate and Analogues
Synthesis 2009, 759 – 766.

•  J. Dernedde, S. Enders, H.-U. Reißig, M. Roskamp, S. Schlecht,* S. Yekta
Inhibition of selectin binding by colloidal gold with functionalized shells
Chem. Commun. 2009, 932 – 934.

B. Bressel, H.-U. Reißig*
A New Approach to Neuraminic Acid Analogues via 1,2-Oxazines
Org. Lett. 2009, 11, 527 – 530.

M. Brasholz, H.-U. Reißig,* R. Zimmer
Sugars, Alkaloids and Heteroaromatics: Exploring Heterocyclic Chemistry with Alkoxyallenes
Acc. Chem. Res. 2009, 42, 45– 56.

C. Venkatesh, H.-U. Reißig*
Model Studies for the Synthesis of Heliquinomycin: Preparation of New Spiroketals
Synthesis 2008, 3605 – 3614.

F. Aulenta, U. K. Wefelsched, I. Brüdgam, H.-U. Reißig*
Nitrogen-Containing Tricyclic and Tetracyclic Compounds via Stereoselective Samarium Diiodide Promoted Cyclizations of Quinolyl-Substituted Ketones – A New Access to Azasteroids
Eur. J. Org. Chem. 2008, 2325 - 2335.

U. K. Wefelscheid, H.-U. Reißig*
Pentacyclic Compounds by Samarium Diiodide-Induced Cascade Cyclizations of Naphthyl-Substituted 1,3-Diones
Adv. Synth. Catal, 2008, 250, 65 – 69.

M. Brasholz, S. Sörgel, C. Azap, H.-U. Reißig*
Rubromycins: Structurally Intriguing, Biologically Valuable, Synthetically Challenging Antitumour Antibiotics
Eur. J. Org. Chem. 2007, 3801 – 3814.

F. Aulenta, M. Berndt, I. Brüdgam, H. Hartl, S. Sörgel, H.-U. Reißig*
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
Chem. Eur. J. 2007, 13, 6047 – 6062.

S. Sörgel, I. Brüdgam, H. Hartl,  H.-U. Reißig*
Crystal structure of 2-bromo-1,4,5,7,8-pentamethoxynaphthalene, C10H2Br(OCH3)5
Z. Kristallogr. NCS 2006, 221, 278 – 280.

S. Sörgel, C. Azap, H.-U. Reißig
Synthesis of Bisbenzannulated Spiroketals – Model Studies for a Modular Approach to Rubromycins
Org. Lett. 2006, 8, 4875 – 4878.

S. Kaden, H.-U. Reißig*
Efficient Approach to the Azaspirane Core of FR 901483
Org. Lett. 2006, 8, 4763 – 4766.

S. Sörgel, C. Azap, H.-U. Reißig*
Preparation of Highly Alkoxy-Substituted Naphthaldehyde Derivatives – A Regioselective Approach to Building Blocks for the Synthesis of Rubromycins
Eur. J. Org. Chem. 2006, 4405  –  4418.

M. A. Chowdhury, H.-U. Reißig*
Syntheses of Highly Substituted Furan and Pyrrole Derivatives via Lithiated 3-Aryl-1-methoxyallenes: Application to the Synthesis of Codonopsinine.
Synlett 2006, 2383 – 2386.

M. Brasholz*, X. Luan, H.-U. Reißig
Towards the Rubromycins: An Efficient Synthesis of a Suitable Isocoumarin Precursor, its Lactam Analogue, and Palladium-Catalyzed Couplings
Synthesis 2005, 3571  –  3580.

S. Kaden, M. Brockmann, H.-U. Reißig*
Synthesis of Enantiopure 2-Substituted Pyrrolidin-3-ones via Lithiated Alkoxyallenes – An Auxilary Based Synthesis of Both Enantiomers of the Antibiotic Anisomycin.
Helv. Chim. Acta 2005, 88, 1826 – 1838.

M. Brasholz, H.-U. Reißig*
An Expedient and Short Synthesis of a 6-Iodo Isocoumarin Building Block for the Rubromycin Family and its First Palladium-Catalyzed Couplings
Synlett 2004, 2736 – 2738.

M. Berndt, I. Hlobilová, H.-U. Reißig*
Stereoselective Formation of Tri- and Tetracycles by Samarium Diiodide-Induced Cyclizations of Naphthyl-Substituted Ketones
Org. Lett. 2004, 6, 957 – 960.
>
O. Flögel, M. G. Okala Amombo, H.-U. Reißig*, G. Zahn, I. Brüdgam, H. Hartl
A Stereoselective and Short Total Synthesis of the Polyhydroxylated γ-Amino Acid (-)-Detoxinine Based on Stereoselective Preparation of Dihydropyrrole Derivatives from Lithiated Alkoxyallenes
Chem. Eur. J. 2003, 9, 1405 – 1415.

W. Schade, H.-U. Reißig*
Stereocontrolled Synthesis of the Taxol C-13 Side Chain: Methyl (2R,3S)-3-Benzoylamino-2-hydroxy-3-phenylpropanoate
J. Prakt. Chem. 1999, 341, 685 – 686.

J. Schnaubelt, B. Frey, H.-U. Reißig*
Formal Total Synthesis of (+)-Dihydromevinolin via a Chelate-Controlled Intramolecular Diels-Alder  Reaction as the Key Step
Helv. Chim. Acta 1999, 82, 666 – 676.

H. Angert, R. Czerwonka, H.-U. Reißig*
Additions of Silyl Enol Ethers to β-Formyl Esters – A Chelate-Controlled Synthesis of the Pheromone (+)-Eldanolide.
Liebigs Ann. 1996, 259 – 263.

K. Paulini, H.-U. Reißig*
Preparation of Novel Lipophilic GABA-Analogues Containing Cyclopropane Rings via Cyclopropanation of N-Silylated Unsaturated Amines
J. prakt. Chem. 1995, 337, 55 – 59.

K. Paulini, H.-U. Reißig*
Synthesis of Dipeptides Containing Novel Cyclopropyl- and Cyclopropenyl-Substituted β- und γ-Amino Acids
Liebigs Ann. Chem. 1994, 549 – 554.

A. G. Beck-Sickinger*, E. Hoffmann, K. Paulini, H.-U. Reißig, K.-D. Willim, H. A. Wieland, G. Jung
High-Affinity Analogues of Neuropeptide Y Containing Conformationally Restricted Non-Proteinogenic Amino Acids
Biochem. Soc. Trans. 1994, 22, 145 – 149.

J. Schnaubelt, R. Zschiesche, H.-U. Reißig*, H. J. Lindner, J. Richter
Synthese von Östronderivaten aus Siloxycyclopropancarbonsäureestern
Liebigs Ann. Chem. 1993, 61 – 70.

K. Paulini, H.-U. Reißig*
Efficient Synthesis of a Novel GABA Analogue Incorporating a Cyclopropene Ring
Synlett 1992, 505 – 506.

R. Zschiesche, T. Hafner, H.-U. Reißig*
Conversion of Polyfunctional Nitroalkanes into Carbonyl Compounds – Synthesis of the Pheromone Chalcogran and of Key Building Blocks for the Macrolides Pyrenophorin and Vermiculine
Liebigs Ann. Chem. 1988, 1169 – 1173.

R. Zschiesche, H.-U. Reißig*
Eine Synthexe von rac-Norbisabolid
Liebigs Ann. Chem. 1987, 387 - 388.

I. Reichelt, H.-U. Reißig*
Neue Chrysanthemumsäurederivative druch Deprotonierung-Alkylierung
Liebigs Ann. Chem. 1985, 650 - 652.

Direct link

Publications

 

•  H.-U. Reißig, M. Domínguez*
N-Methylpyridinium-4-phenolates: Generation of a Betaine Dye Library Bearing Different Spacer Units and Their Solvatochromism
ChemistrySelect 2016, 1, 5270 – 5275.

P. Hommes, H.-U. Reißig*
Synthesis of Highly Functionalized 2,2´-Bipyridines by Cyclocondensation of β-Ketoenamides – Scope and Limitations
Beilstein J. Org. Chem. 2016, 12, 1170 – 1177.

•  P. Hommes, H.-U. Reißig*
Functionalization of Highly Substituted 2,2´:6,6´,2´´-Terpyridine Derivatives
Eur. J. Org. Chem. 2016, 338 – 342.

•  G. Podolan, L. Hettmanczyk, P. Hommes, B. Sarkar,* H.-U. Reißig*
Synthesis and (Spectro)electrochemistry of New Ferrocenyl-Substituted Pyridine Derivatives
Eur. J. Org. Chem. 2015, 7317 – 7323.

•  D. Trawny, M. Quennet, N. Rades, D. Lentz, B. Paulus, H.-U. Reissig*
Syntheses, Structures and Conformational Dynamics of 1,3,5-Tris(3‘‘-ethynylbi-phenyl-2‘-yl)benzene Derivatives
Eur. J. Org. Chem. 2015, 4667 – 4674.

M. Gensler, C. Eidamshaus, M. Taszarek, H.-U. Reissig, J. P. Rabe*
Mechanical Stability of Bivalent Transition Metal Complexes Analyzed by Single-Molecule Force Spectroscopy
Beilstein J. Org. Chem.
2015, 11, 817 – 827.

J. Dash, D. Trawny, J. P. Rabe, H.-U. Reissig*
C3-Symmetric Pyridine and Bipyridine Derivatives: Simple Preparation by Cyclocondensation and 2D Self-Assembly at a Solution-Graphite Interface
Synlett 2015, 26, 1486 – 1489.

M. Gensler, C. Eidamshaus, A. Galstyan, E.-W. Knapp*, H.-U. Reißig, J. P. Rabe*
Mechanical Rupture of Mono- and Bivalent Transition Metal Complexes in Experiment and Theory
J. Phys. Chem. C 2015, 119, 4333 – 4343.

D. Trawny, P. Schlexer, K. Steenbergen, J. P. Rabe*, B. Paulus*, H.-U. Reißig*
Dense or Porous Packing? Two-Dimensional Self-Assembly of Star-Shaped Mono-, Bi-, and Terpyridine Derivatives
ChemPhysChem 2015, 16, 949 – 953.

D. Trawny, V. Kunz, H.-U. Reißig*
Modular Syntheses of Star-Shaped Pyridine, Bipyridine, and Terpyridine Derivatives by Employing Sonogashira Reactions
Eur. J. Org. Chem. 2014, 6295 – 6302.

D. Trawny, L. Vandromme, J. P. Rabe,* H.-U. Reissig*
The Side Chain Makes the Difference: Investigation of the 2D Self-Assembly of 1,3,5-Tris[4-(4-pyridinyl)phenyl]benzene Derivatives by Scanning Tunneling Microscopy
Eur. J. Org. Chem. 2014, 4985 – 4992.

D. Gladow, S. Doniz-Kettenmann, H.-U. Reißig*
1,3-Dipolar Cycloadditions of Ethyl 2-Diazo-3,3,3-trifluoropropanoate to Alkynes and [1,5] Sigmatropic Rearrangements of the Resulting 3H-Pyrazoles: Synthesis of Mono-, Bis- and Tris(trifluoromethyl)-Substituted Pyrazoles
Helv. Chim. Acta, 2014, 97, 808 – 821.

D. Gladow, H.-U. Reißig*
Perfluoroalkyl-Substituted Thiophenes and Pyrroles from Donor-Acceptor Cyclopropanes and Heterocumulenes: Synthesis and Exploration of their Reactivity
J. Org. Chem. 2014, 79, 4492 – 4502.

 L. Bouché, H.-U. Reißig*
Synthesis of Di- and Trivalent Carbohydrate Mimetics with Oxepane Substructure by Employing Copper-Catalyzed [3+2] Cycloadditions of Alkynes with Azidooxepanes
Eur. J. Org. Chem. 2014, 3697 – 3703.

 •  M. Domínguez, H.-U. Reißig*
New 4-Pyridyl Nonaflates as Precursors for Push-Pull Solvatochromik Dyes
Synthesis 2014, 46, 1110 – 1106.

M. K. Bera, M. Domínguez, P. Hommes, H.-U. Reißig*
The Flögel-Three-Component Reaction with Dicarboxylic Acids - An Approach to Bis(β-alkoxy-β - ketoenamides) for the Synthesis of Complex Pyridine and Pyrimidine Derivatives
Beilstein J. Org. Chem. 2014, 10, 394 – 404.

M. K. Bera, S. L. Gholap, P. Hommes, K. Neuthe, D. Trawny, J. P. Rabe, D. Lentz, R. Zimmer, H.-U. Reißig*
Synthesis and Properties of Branched Oligo(2-thienyl)- and Oligo(2,2’-bithien-5-yl)-Substituted Pyridine Derivatives
Adv. Synth. Catal. 2013, 355, 3463 – 3474

•   P. Hommes, S. Berlin, H.-U. Reißig*
Trimethylsilyl Trifluoromethanesulfonate-Promoted Cyclocondensation of b-Keto-enamides and Subsequent Nonaflation to Pyrid-2-yl and Pyrid-4-yl Nonaflates as Flexible Precursors for Polysubstituted Pyridines
Synthesis 2013, 45, 3288 – 3294.

•  S. L. Gholap, P. Hommes, K. Neuthe, H.-U. Reißig*
Per(2-thienyl)pyridines: Synthesis and Properties
Org. Lett. 2013, 15, 318 – 321.

•  T. Lechel, G. Podolan, B. Brusilowskij, C. A. Schalley, H.-U. Reißig*
Unexpected One-Step Formation of Iodo[1,3]dioxolo[4,5-c]pyridine Derivatives by a Hofmann-Löffler-Freytag Reaction: Studies on the Synthesis of a Pyridine-Containing Macrocycle
Eur. J. Org. Chem. 2012, 5685 – 5692
.
•  C. Eidamshaus, P. Hommes, H.-U. Reißig*
Palladium-Catalyzed Coupling of Pyrid-4-yl Nonaflates with Methyl Diazoacetate
Synlett 2012, 1670 – 1674.

•  C. Eidamshaus, T. Triemer, H.-U. Reißig*
Synthesis of 4-Quinolones via Cyclocondensation of Substituted ortho-Amidoacetophenones: A Refit to the Camps Cyclization by Applying Trimethylsilyl Trifluoromethanesulfonate/Triethylamine
Synthesis 2011, 3261 – 3266.

•  I. Linder, M. Gerhard, L. Schefzig, M. Andrä, C. Bentz, H.-U. Reißig,* R. Zimmer
A Modular Synthesis of Functionalized Pyridines through Lewis-Acid-Mediated and Microwave-Assisted Cycloadditions between Azapyrylium Intermediates and Alkynes
Eur. J. Org. Chem. 2011, 6070 – 6078.

•  C. Eidamshaus, H.-U. Reißig*
A Chiral Pool Strategy for the Synthesis of Enantiopure Hydroxymethyl-Substituted Pyridine Derivatives
Eur. J. Org. Chem. 2011, 6056 – 6069

•  M. K. Bera, P. Hommes, H.-U. Reißig*
In Search of Oligo(2-thienyl)-Substituted Pyridine Derivatives: A Modular Approach to Di-, Tri- and Tetra(2-thienyl)pyridines
Chem. Eur. J. 2011, 17, 11838 – 11844.

•  P. Hommes, P. Jungk, H.-U. Reißig*
Four-Component Synthesis of Functionalized 2,2’-Bipyridines Based on the Blaise Reaction
Synlett 2011, 2311 – 2314.

•  C. Eidamshaus, R. Kumar, M. K. Bera, H.-U. Reißig*
A Practical Two-Step Procedure for the Preparation of Enantiopure Pyridines: Multicomponent Reactions of Alkoxyallenes, Nitriles and Carboxylic Acids followed by a Cyclocondensation Reaction
Beilstein J. Org. Chem. 2011, 7, 962   975.

•  T. Lechel, M. Gerhard, D. Trawny, Boris Brusilowskij, L. Schefzig, R. Zimmer, J. P. Rabe, D. Lentz, C. A. Schalley, H.-U. Reißig*
Synthesis of 5-Acetyloxazoles and 1,2-Diketones from β-Alkoxy-β-ketoenamides and Their Subsequent Transformations
Chem. Eur. J. 2011, 7480 – 7491.

•  D. Mollenhauer, J. Floß, H.-U. Reißig, E. Voloshina, B. Paulus*
Accurate Quantum-Chemical Description of Gold Complexes with Pyridine and its Derivatives
J. Comput. Chem. 2011, 32, 1839 – 1845.

•  T. Lechel, H.-U. Reißig*
Synthesis of Heterocycles via Alkoxyallenes
Pure Appl. Chem. 2010, 82, 1835 – 1844.

•  M. K. Bera, H.-U. Reißig*
A Route to Alkenyl-Substituted 4-Hydroxypyridine and Pyrimidine Derivatives via Three-Component Access to β-Alkoxy-β-ketoenamides
Synthesis 2010, 2129 – 2138.

•  T. Lechel, J. Dash, C. Eidamshaus, I. Brüdgam, D. Lentz, H.-U. Reißig*
A Three-component Synthesis of β-Alkoxy-β-keto-enamides - Flexible Precoursors for 4-Hydroxypyridine Derivatives and their Palladium-catalysed Reactions
Org. Biomol. Chem. 2010, 8, 3007 – 3014.

•  T. Lechel, I. Brüdgam, H.-U. Reißig*
Preparation of pyridine-3,4-diols, their crystal packing and their use as precursors for palladium-catalyzed cross-coupling reactions
Beilstein Journal of Organic Chemistry 2010, 6, No. 42.

T. Lechel, J. Dash, P. Hommes, D. Lentz, H.-U. Reißig*
Three-Component Synthesis of Perfluoroalkyl- or Perfluoroaryl-Substituted 4-Hydroxypyridine Derivatives and Their Palladium-Catalyzed Coupling Reactions
J. Org. Chem. 2010, 75, 726 – 732.

T. Lechel, H.-U. Reißig*
New 5-Alkoxypyrimidine Derivatives from β-Alkoxy β-Keto Enamides and Ammonium Salts
Eur. J. Org. Chem. 2010, 2555 – 2564.

R. Zimmer, E. Schmidt, M. Andrä, M.-A. Duhs, I. Linder, H.-U. Reißig*
Palladium-catalyzed cross coupling reactions of 4-bromo-6H-1,2-oxazines
Beilstein Journal of Organic Chemistry 2009, 5, No. 44.

J. Dash, H.-U. Reißig*
A New and Flexible Synthesis of 4-Hydroxypyridines: Rapid Access to Caerulomycins A, E and Functionalized Terpyridines
Chem. Eur. J. 2009, 15, 6811  –  6814.

C. Eidamshaus, H.-U. Reißig*
Hihgly Funtionalized Enantiopure 4-Hydroxypyridine Derivatives by a Versatile Three-Component Synthesis
Adv. Synth. Catal. 2009, 351, 1162 - 1166.

T. Lechel, S. Möhl, H.-U. Reißig*
A Concise Synthesis of Alkoxy-Substituted Pyrimidine Derivatives Based upon a Three-Component Access to Functionalized Enamides
Synlett 2009, 1059 1062.

J. Dash, I. Brüdgam, H. Hartl, H.-U. Reißig*
Crystal structure of 1,4-bis[3-methoxy-4(4-methoxyphenyl)-6-(trifluoromethyl)-pyridin-2-yl]benzene, C34H26F6N2O4Z.
Kristallogr. NCS
2008, 223, 347.

T. Lechel, J. Dash, I. Brüdgam, H.-U. Reißig*
Novel Furopyridine Derivatives via Sonogashira Reactions of Functionalized Pyridines
Eur. J. Org. Chem. 2008, 3647– 3655.

L. Vandromme, H.-U. Reißig*, S. Gröper, J. P. Rabe
Practical Routes to New 2,6-Disubstituted Pyridine Derivatives
Eur. J. Org. Chem. 2008, 2049 - 2055.

J. Dash, T. Lechel, H.-U. Reißig*
Scope of a Novel Three-Component Synthesis of Highly Functionalized Pyridines
Org. Lett. 2007, 9, 5541 – 5544.

Patent:
O. Flögel, H.-U. Reißig
Substituierte Pyridine
Deutsches Patentamt (DE 10336497 vom 03.03.2005)

O. Flögel, J. Dash, I. Brüdgam, H. Hartl, H. U. Reißig*
A New Color of the Synthetic Chameleon Methoxyallene: Synthesis of Trifluoromethyl-Substituted Pyridinol Derivatives – An Unusual Reaction Mechanism, a Remarkable Crystal Packing, and First Palladium-Catalyzed Coupling Reactions
Chem. Eur. J. 2004, 10, 4283 – 4290.

Direct link

Publications

•  C. N. Rao, C. Bentz, H.-U. Reissig*
Lithium Bromide/Water as Additives in Dearomatizing Samarium-Ketyl (Hetero)Arene Cyclizations
Chem. Eur. J. 2015, 21, 15951 – 15954.

C. Beemelmanns, H.-U. Reissig*
Strychnine as Target, Samarium Diiodide as Tool: A Personal Story
Chem. Rec. 2015, 15, 872 – 885.

•  C. Beemelmanns, H.-U. Reißig*
Evolution of a Short Route to Strychnine by Using the Samarium-Diiodide-Induced Cascade Cyclization as a Key Step
Chem. Eur. J. 2015, 21, 8416 – 8425.

C. N. Rao, D. Lentz, H.-U. Reißig*
Synthese polycyclischer tertiärer Carbinamine durch Samariumdiiodid-vermittelte Cyclisierungen von Indolylsulfinylimien
Angew. Chem. 2015, 127, 2788 – 2792.

C. N. Rao, D. Lentz, H.-U. Reißig*
Synthesis of Polycyclic Tertiary Carbinamines by Samarium Diiodide Mediated Cyclizations of Indolyl Sulfinyl Imines
Angew. Chem. Int. Ed. 2015, 54, 2750 – 2753.

•  M. Kandziora, H.-U. Reißig*
Synthesis of Rigid p-Terphenyl-Linked Carbohydrate Mimetics
Beilstein J. Org. Chem. 2014, 10, 1749 – 1758.

C. Beemelmanns, S. Gross, H.-U. Reißig*
Towards the Core Structure of Strychnos Alkaloids Using Samarium Diiodide-Induced Reactions of Indole Derivatives
Chem. Eur. J. 2013,19, 17801 – 17808.

A. Niermann, J. E. Grössel, H.-U. Reißig*
New Thiochromans via Reductive Cyclization of Thiophenol Derivatives
Synlett 2013, 177 – 180.

M. Jasiński,T. Watanabe, H.-U. Reißig*
Samarium Diiodide Promoted Reduction of 3,6-Dihydro-2H-1,2-oxazines: Competition of 1,4-Amino Alcohol Formation and Ring Contraction to Pyrrole Derivatives
Eur. J. Org. Chem. 2013, 605 – 610.

M. Berndt, A. Hölemann, A. Niermann, C. Bentz, R. Zimmer, H.-U. Reißig*
Replacement of HMPA in Samarium Diiodide Promoted Cyclizations and Reactions of Organolithium Compounds
Eur. J. Org. Chem. 2012, 1299 – 1302.

C. Beemelmanns, D. Lentz, H.-U. Reißig*
Samarium Diiodide Induced Cyclizations of γ-, δ- and ε-Indolyl Ketones: Reductive Coupling, Intermolecular Trapping, and Subsequent Transformations of Indolines
Chem. Eur. J. 2011, 17, 9720   9730.

C. Beemelmanns, H.-U. Reißig*
Samarium diiodide induced ketyl-(het)arene cyclisations towards novel N-heterocycles
Chem. Soc. Rev. 2011, 40, 2199 – 2210.

A. Niermann, H.-U. Reißig*
Influence of Geminal Disubstitution on Samarium Diiodide Induced Reductive Cyclizatons of γ-Aryl Ketones
Synlett 2011, 525 – 528.

C. Beemelmanns, H.-U. Reißig*
New Samarium Diiodide-Induced Cyclizations
Pure Appl. Chem. 2011, 83, 507 – 517.

•  J. Saadi, I. Brüdgam, H.-U. Reißig*
Highly Substituted Benzannulated Cyclooctanol Derivatives by Samarium Diiodide-Induced Cyclizations
Beilstein Journal of Organic Chemistry 2010, 6, No. 141, (1229 – 1245).

•  C. Beemelmanns, H.-U. Reißig*
Eine kurze formale Strychnin-Totalsynthese mit einer Samariumdiiodid-induzierten Kaskadenreaktion als Schlüsselschritt
Angew. Chem. 2010, 122, 8195  –  8199.

C. Beemelmanns, H.-U. Reißig*
A Short Formal Total Synthesis of Strychnine with a Samarium Diiodide Induced Cascade Reaction as the Key Step
Angew. Chem. Int. Ed. 2010, 49, 8021  –  8025.

•  U. K. Wefelscheid, H.-U. Reißig*
Synthesis of New Steroid Analogues by Samarium Diiodide Induced Cyclisations of γ-Naphthyl 1,3-Diones
Tetrahedron: Asymmetry 2010, 21, 1601 – 1610.

•  C. Beemelmanns, V. Blot, S. Gross, D. Lentz, H.-U. Reißig*
Highly Diastereoselective Samarium Diiodide Induced Ketyl Cyclisations of Indole and Pyrrole Derivatives – Scope and Limitations
Eur. J. Org. Chem. 2010, 2716 – 2732.

C. Beemelmanns, H.-U. Reißig*
Highly diastereoselective samarium diiodide induced cyclizations of new 3-substituted indole derivatives
Org. Biomol. Chem. 2009, 7, 4475 - 4480.

J. Saadi, H.-U. Reißig*
Scope and Limitations of Samarium Diiodide Induced Cyclizations of Alkenyl-Substituted γ-Keto Esters to Benzannulated Cyclooctanol Derivatives
Synlett 2009, 2089 - 2092.

J. Saadi, D. Lentz, H.-U. Reißig*
Medium-Sized Carbocycles by Samarium Diiodide-Induced Carbonyl-Alkene Cyclizations
Org. Lett. 2009, 11, 3334 - 3337.

U. K. Wefelscheid, M. Berndt, H.-U. Reißig*
Samarium Diiodide Mediated Ketyl-Aryl Couplings – Influence of Substituents and Trapping Experiments
Eur. J. Org. Chem. 2008, 3635– 3646.

R. S. Kumaran, I. Brüdgam, H.-U. Reißig*
Modular and Stereoselective Synthesis of Hydroxylated Angularly Fused Tricyclic Piperidine Derivatives via Samarium Diiodide-Mediated Cyclization
Synlett, 2008, 991 – 994.

F. Aulenta, U. K. Wefelscheid, I. Brüdgam, H.-U. Reißig*
Nitrogen-Containing Tricyclic and Tetracyclic Compounds via Stereoselective Samarium Diiodide Promoted Cyclizations of Quinolyl-Substituted Ketones – A New Access to Azasteroids
Eur. J. Org. Chem. 2008, 2325 - 2335.

U. K. Wefelscheid, H.-U. Reißig*
Pentacyclic Compounds by Samarium Diiodide-Induced Cascade Cyclizations of Naphthyl-Substituted 1,3-Diones
Adv. Synth. Catal, 2008, 350, 65 – 69.

U. K. Wefelscheid, I. Brüdgam, H. Hartl, H.-U. Reißig*
Crystal structure of (8S*,9S*,13S*,14R*,17S*)-estra-1(10),2,4,6-tetraene-
14,17-diol monohydrate, C
18H22O2 H2O
Z. Kristallogr. NCS 2007, 222, 467 – 468.

U. K. Wefelscheid, I. Brüdgam, H.-U. Reißig*
Crystal structure of (8S*,9S*,13R*,14R*,17S*)-9,17-cycloestra-1(10),
2,4,6-tetraene-14,17-diol trihydrate, C
18H20O23H2O
Z. Kristallogr. NCS 2007, 222, 465 – 466.

F. Aulenta, M. Berndt, I. Brüdgam, H. Hartl, S. Sörgel, H.-U. Reißig*
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
Chem. Eur. J. 2007, 13, 6047 – 6062.

V. Blot, H.-U. Reißig*
Efficient Synthesis of Medium-Sized Rings Incorporating Indole or Pyrrole Units
by Samarium Diiodide Induced Cyclizations

Eur. J. Org. Chem. 2006, 4989 - 4992.

F. Aulenta, H.-U. Reißig
Heck Reactions of Quinoline-Derived Nonaflates
Synlett 2006, 2993 – 2996.

V. Blot, H.-U. Reißig*
Highly Substituted Dihydroindole Derivatives by Intermolecular Couplings of
Samarium Ketyls and Indoles

Synlett 2006, 2763 - 2766.

H.-U. Reißig*, F. A. Khan, R. Czerwonka, C. U. Dinesh, A. L. Shaikh, R. Zimmer
Benzannulated Cyclooctanol Derivatives by Samarium Diiodide Induced
Intramolecular Carbonyl-Alkene Coupling - Scope, Limitations, Stereoselectivity

Eur. J. Org. Chem. 2006, 4419 - 4428.

F. Aulenta, A. Hölemann, H.-U. Reißig*
Samarium Diiodide Induced Reactions of Cyclopropyl Ketones: Reductive Ring
Cleavage and Dimerization Leading to 1,8-Diketones - Scope, Limitations, Mechanism
Eur. J. Org. Chem. 2006, 1733 - 1739.

A. Hölemann, H.-U. Reißig*
Samarium Diiodide in the Synthesis of Medium-Sized Rings - Carbocycles and Heterocycles by Intramolecular Addition of Samarium Ketyls to Alkynes
Synlett 2004, 2732 - 2735.

A. Hölemann, H.-U. Reißig*
Regioselective Samarium Diiodide-Induced Couplings of Carbonyl Compounds with
1,3-Diphenylallene and Alkoxyallenes - A New Route to 4-Hydroxy 1-Enol Ethers

Chem. Eur. J. 2004, 10, 5493 - 5506.

A.  Hölemann, H.-U. Reißig*
Synthesis of New Furan Derivatives and 4-Hydroxy Aldehydes from 4-Hydroxy
1-Enol Ethers

Synthesis 2004, 1963 – 1970.

M. Berndt, I. Hlobilová, H.-U. Reißig*
Stereoselective Formation of Tri- and Tetracycles by Samarium Diiodide-
Induced Cyclizations of Naphthyl-Substituted Ketones

Org. Lett. 2004, 6, 957 - 960.
 
A. Hölemann, I. Brüdgam, H. Hartl*, H.-U. Reißig
Crystal Structure of cis-(5E)-Phenylmethylidenedecahydro-4aH-benzo[a]cyclo-
hepten-4a-ol, C18H24O

Z. Kristallogr. NCS 2004, 219, 59 - 60.
 
S. Groß, I. Brüdgam, H. Hartl*, H.-U. Reißig
Crystal Structure of (9aRS,10SR,10aRS)-8-Methoxy-10-methyl-
1,2,3,5,7,9a,10,10a-octahydropyrrolo[1,2-b]isoquinoline-10-ol, C14H21NO2

Z. Kristallogr. NCS 2004, 219, 57 - 58.
 
S. Groß, I. Brüdgam, H. Hartl*, H.-U. Reißig
Crystal Structure of (4SR,4aSR)-1-Acetyl-4-hydroxy-4,8-dimethyl-1,2,3,4,4a,7-
hexahydroquinoline, C13H19NO2

Z. Kristallogr. NCS 2004, 219, 55 - 56.
 
S. Groß, I. Brüdgam, H. Hartl*, H.-U. Reißig
Crystal Structure of (2RS,4SR,4aSR)-1-Acetyl-2-(1-methylethyl)-4-hydroxy-
4-methyl-1,2,3,4,4a,7-hexahydroquinoline, C15H22NO2

Z. Kristallogr. NCS 2004, 219, 53 - 54.
 
M. Berndt, I. Brüdgam, H. Hartl*, H.-U. Reißig
Crystal Structure of 1-Isopropyl-15-oxatetracyclo[11.2.1.02,11.05,10]hexadeca-
3,5(10),6,8-tetraen-14-one, C18H20O2

Z. Kristallogr. NCS 2004, 219, 51 - 52.
 
M. Berndt, I. Brüdgam, H. Hartl*, H.-U. Reißig
Crystal Structure of (1aSR,5bRS,7aSR,10aRS,10bSR,10cRS)-1a,5b,6,7,7a,8,9,10,
10b,10c-Decahydro-10aH-cyclopenta[1,2]phenanthro[9,10-b] oxiren-10a-ol, C17H20O2

Z. Kristallogr. NCS 2004, 219, 49 - 50.
 
M. Berndt, I. Brüdgam, H. Hartl*, H.-U. Reißig
Crystal Structure of (2SR,1'RS)-3-(1-Naphthyl)-2-(2-oxocyclopentyl)-propionic
acid methyl ester, C19H20O3

Z. Kristallogr. NCS 2004, 219, 47 - 48.

 

M. Berndt, S. Groß, A. Hölemann, H.-U. Reißig*
New Samarium Diiodide-Induced Ketyl Couplings – From Analogous Reactions to
Serendipitously Discovered Processes

Synlett 2004, 422 – 438.  

S. Groß, H.-U. Reißig*
Novel Stereoselective Syntheses of Highly Functionalized Benzannulated
Pyrrolizidines and Indolizidines by Samarium Diiodide-Induced Cyclizations of
Indole Derivatives

Org. Lett. 2003, 5, 4305 - 4307.
 
A. Hölemann, H.-U. Reißig*
Samarium Diiodide-Induced Couplings of Carbonyl Compounds with Methoxyallene
Leading to 4-Hydroxy 1-Enol Ethers

Org. Lett. 2003, 5, 1463 - 1466.

 

S. Groß, H.-U. Reißig*
Samarium Diiodide-Induced Diastereoselective Synthesis of Hexahydroquinoline
Derivatives

Synlett 2002, 2027 - 2030.
 
O. Rademacher*, R. Zimmer, C. U. Dinesh, H. U. Reißig
Crystal structure of 2SR,5SR,5aSR,11bSR-5-Methyl-1,5,5a,11b-
tetrahydro-2,5-methanonaphtho[2,1-c]oxepin-3(2H)-one, C16H16O2

Z. Kristallogr. NCS 2002, 217, 425 - 426.
 
O. Rademacher*, R. Zimmer, C. U. Dinesh, H. U. Reißig
Crystal structure of Methyl 4aSR,5RS,12aRS-12a-Hydroxy-
1,2-3,4,4a,5,6,11,12,12a-decahydro-dibenzo[a,e][8]annulene-5-carboxylate, C18H24O3

Z. Kristallogr. NCS 2002, 217, 423 - 424. 

 

O. Rademacher*, M. Berndt, H.-U. Reißig
Crystal Structure of 4R*,4aS*,5S*-5-Hydroxy-4-(1-hydroxy-1-methylethyl)-5-
methyl-4,4a,5,6,7,8-hexahydronaphthalene-2-carbonitrile—water (1/1), C15H21NO2  H2
O.
Kristallogr.
NCS 2001, 216, 593 – 594.

D. Lentz*, E. Nandanan, H.-U. Reißig
Crystal Structure of 6S*,8S*-9-Butyl-8-hydroxy-8-isopropyl-5,6,7,8-tetra­
hydro­benzo­cyclo­octene-6-carboxylate, C21H30NO3
Z. Kristallogr. NCS 2001, 216, 525 – 526.  

Berndt, H.-U. Reißig*
Substituent Effects in Samarium Diiodide-Induced 6-trig Cyclizations of γ-Aryl­
ketones to Functionalized Hexahydronaphthalene Derivatives
Synlett 2001, 1290 – 1292.  

C. U. Dinesh, H.-U. Reißig, O. Rademacher*
Crystal structure of methyl 4aR*,4bR*,8aS*,9R*-1-cyano-4b-hydroxy-2,4a,
4b,5,6,7,8,8a,9, 10-decahydro- phenanthrene-9-carboxylate, C17H21NO3

Z. Kristallogr. NCS 2000, 215, 615 - 616.

E. Nandanan, C. U. Dinesh, H.-U. Reißig*
Competition between Novel 8-endo-dig and 6-trig Cyclizations of Samarium
Ketyls Leading either to Benzannulated Cyclooctene or to Hexahydronaphthalene
Derivatives

Tetrahedron 2000, 56, 4267 - 4277.
 
R. Zimmer, G. Zahn*, F. A. Khan, H.-U. Reißig*
Configurational Analysis of 14,14-Dimethyl-12-oxatricyclo[9.2.1.03,8]tetradeca-
3,5,7-trien-13-one

Acta Crystallogr. Sect. C 1999, 55, 1941 - 1943.

C. U. Dinesh, H.-U. Reißig*
Eine neue Samariumdiiodid-induzierte Reaktion: intramolekularer Angriff von
Ketylradikalanionen auf Arylsubstituenten unter Bildung von 1,4-Cyclohexadienderivaten

Angew. Chem. 1999, 111, 874 - 876.

  C. U. Dinesh, H.-U. Reißig*
A New Samarium Diiodide Induced Reaction: Intramolecular Attack of Ketyl Radical Anions on Aryl Substituents with Formation of 1,4-Cyclohexadiene Derivatives
Angew. Chem. Int. Ed. 1999, 38, 789 - 791.

F. A. Khan, R. Czerwonka, R. Zimmer, H.-U. Reißig*
A Novel Sm(II)-Induced Route to Highly Substituted Benzannulated
Cyclooctanol Derivatives

Synlett 1997, 995 - 997.
Direct link

Synthesis of Carbohydrates and Carbohydrate Mimetics

Publications 

M. Jasiński*, G. Utecht, A. Fruziński, H.-U. Reißig
Three-Step Synthesis of 3-Aminoseptanoside Derivatives Using Lithiated Methoxyallene and δ-Siloxynitrones
Synthesis 2016, 48, 893 – 905.

J. Salta, J. Dernedde, H.-U. Reißig*
Synthesis of Multivalent Carbohydrate Mimetics with Aminopolyol End Groups and their Evaluation as L-Selectin Inhibitors
Beilstein J. Org. Chem. 2015, 11, 638 – 646.

J. Salta, H.-U. Reißig*
Synthesis of Divalent Carbohydrate Mimetics by Reductive Amination with Enantiopure 1,2-Oxazines as Precursors
Synthesis 2015, 47, 1893 – 1898.

M. Kandziora, E. Mucha, S. P. Zucker, H.-U.Reißig*
Syntheses of Mono- and Divalent C-Aminoglycosides Using 1,2-Oxazine Chemistry and Olefin Metathesis
Synlett 2015, 26, 367 – 374.

M. Kandziora, H.-U. Reißig*
Preparation of Multivalent Carbohydrate Mimetics Based on Enantiopure 1,2-Oxazines by Sonogashira Coupling and Subsequent Reductive Ring-Opening
Eur. J. Org. Chem. 2015, 370 – 377.

L. Bouché, M. Kandziora, H.-U. Reißig*
Synthesis of New Enantiopure Poly(hydroxy)aminooxepanes as Building Blocks for Multivalent Carbohydrate Mimetics
Beilstein J. Org. Chem. 2014, 10, 213 – 223.

M. Jasiński, Dieter Lentz, E. Moreno-Clavijo, H.-U. Reißig*
Application of L-Erythrose-Derived Nitrones in the Synthesis of Polyhydroxylated Compounds via 3,6-Dihydro-2H-1,2-oxazine Derivatives
Eur. J. Org. Chem. 2012, 3304 – 3316.

M. Jasiński, Dieter Lentz, H.-U. Reißig*
Carbohydrate-Auxiliary Assisted Preparation of Enantiopure 1,2-Oxazine Derivatives and Aminopolyols
Beilstein J. Org. Chem. 2012, 8, 662-674.

L. Bouché, H.-U. Reißig*
Synthesis of Novel Carbohydrate Mimetics via 1,2-Oxazines
Pure Appl. Chem. 2012, 84, 23 – 36.

M. Roskamp, S. Enders, F. Pfrengle, S. Yekta. V. Dekaris, J. Dernedde, H.-U. Reißig, S. Schlecht*
Multivalent Interaction and Selectivities in Selectin Binding of Functionalized Gold Colloids Decorated with Carbohydrate Mimetics
Org. Biomol. Chem. 2011, 9, 7448 – 7456.

V. Dekaris, R. Pulz, A. Al-Harrasi, D. Lentz, H.-U. Reißig*
Stereoselective Synthesis of Aza, Amino and Imion Sugar Derivatives by Hydroboration of 3,6-Dihydro-2H-1,2-oxazines as Key Reaction
Eur. J. Org. Chem. 2011, 3210 – 3219.

G. Semini, A. Hildmann, H.-U. Reißig, W. Reutter, K. Danker*
The Novel Synthetic Ether Lipid Inositol-C2-PAF Inhibits Phosphorylation of the Tyrosine Kinases Src and FAK Independent of Integrin Activation in Transformed Skin Cells
Biochemical Pharmacology 2011, 81, 985 – 995.

A. Al-Harrasi, L. Bouché, R. Zimmer, H.-U. Reißig*
β-Alkoxy-γ-amino Aldehydes by Internal Redox Ring Cleavages of Carbohydrate-Derived Enantiopure 1,2-Oxazines and Preparation of Heterocycles with Aminopolyol Side Chain
Synthesis 2011, 109 – 118.

F. Pfrengle, H.-U. Reißig*
Internally Protected Amino Sugar Equivalents from Enantiopure 1,2-Oxazines: Synthesis of Variably Configured Carbohydrates with C-Branched Amino Sugar Units
Chem. Eur. J. 2010, 16, 11915  –  11925.

F. Pfrengle, H.-U. Reißig*
Addition of Lithiated Enol Ethers to Nitrones and Subsequent Lewis Acid Induced Cyclizations to Enantiopure 3,6-Dihydro-2H-pyrans – an Approach to Carbohydrate Mimetics
Beilstein Journal of Organic Chemistry 2010, 6, No. 75.

F. Pfrengle, H.-U. Reißig*
Amino Sugars and their Mimetics via 1,2-Oxazines
Chem. Soc. Rev., 2010, 39, 549 – 557.

A. Al-Harrasi, S. Fischer, R. Zimmer, H.-U. Reißig*
Ring Enlargement of Carbohydrate-Derived 1,2-Oxazines to Enantiopure 5-Bromo-1,2-oxazepines and Subsequent Palladium-Catalyzed Reactions
Synthesis 2010, 304 – 314.

V. Dekaris, B. Bressel, H.-U. Reißig*
Acid Mediated Transformations of Enantiopure 3,6-Dihydro-2H-1,2-oxazines into Functionalized Aminotetrahydrofuran Derivatives
Synlett 2010, 47 – 50.

V. Dekaris, H.-U. Reißig*
Stereocontrolled Syntheses of Enantiopure Polyhydroxylated Azetidines via 1,2-Oxazines
Synlett 2010, 42 – 46.

F. Pfrengle, D. Lentz, H.-U. Reißig*
A New Ring Closure Approach to Enantiopure 3,6-Dihydro-2H-pyrans: Stereodivergent Access to Carbohydrate Mimetics
Org. Lett. 2009, 11, 5534 – 5537.

A. Al-Harrasi, F. Pfrengle, V. Prisyazhnyuk, S. Yekta, P. Koóš, H.-U. Reißig*
Enantiopure Aminopyrans by a Lewis Acid Promoted Rearrangement of 1,2-Oxazines: Versatile Building Blocks for Oligosaccharide and Sugar Amino Acid Mimetics
Chem. Eur. J. 2009, 15, 11632  –  11642

M. Brasholz, H.-U. Reißig*
Alkoxyallene-Based De Novo Synthesis of Rare Deoxy Sugars: New Routes to L-Cymarose, L-Sarmentose, L-Diginose and L-Oleandrose
Eur. J. Org. Chem. 2009, 3595– 3604.

•  F. Pfrengle, D. Lentz, H.-U. Reißig*
Stereodivergente De-novo-Synthese verzweigter Aminozucker durch Lewis-Säure-induzierte Umlagerung von 1,2-Oxazinen
Angew. Chem. 2009, 121, 3211 - 3215.

  F. Pfrengle, D. Lentz, H.-U. Reißig*
Stereodivergent De novo Synthesis of Branched Amino Sugars by Lewis Acid promoted Rearrangement of 1,2-Oxazines
Angew. Chem. Int. Ed. 2009, 48, 3165 - 3169.

•  B. Bressel, H.-U. Reißig*
A New Approach to Neuraminic Acid Analogues via 1,2-Oxazines
Org. Lett. 2009, 11, 527 – 530.

•  F. Pfrengle, A. Al-Harrasi, I. Brüdgam, H.-U. Reißig*
Unusual Enantiopure Heterocyclic Skeletons via Lewis Acid Promoted Rearrangements of 1,3-Dioxolanyl-Substituted 1,2-Oxazines
Eur. J. Org. Chem. 2009, 282 – 291.

E. Hýrošovà, L. Fišera,* M. Medvecký, H.-U. Reißig, A. Al-Harrasi, M. Koòš
From sugars to modified nucleosides
ARKIVOC 2009 (ix), 122 - 142.

B. Bressel, B. Egart, A. Al-Harrasi, R. Pulz, H.-U. Reißig,* I. Brüdgam
Acid-Induced and Reductive Transformations of Enantiopure 3,6-Dihydro-2H-1,2-oxazines – Synthesis of Dideoxyamino Carbohydrate Derivatives
Eur. J. Org. Chem. 2008, 467 – 474.

S. Yekta, V. Prisyazhnyuk, H.-U. Reißig*
Simple Modifications of Enantiopure 1,2-Oxazines Leading to Building Blocks for Carbohydrate and Peptide Mimetics
Synlett 2007, 2069 – 2072.

M. Brasholz, H.-U. Reißig*
Oxidative Spaltung von 3-Alkoxy-2,5-dihydrofuranen und ihre Anwendung in der De-novo-Synthese seltener Monosaccharide am Beispiel von L-Cymarose
Angew. Chem. 2007, 119, 1659 – 1662; Angew. Chem. Int. Ed. 2007, 46, 1634  –  1637.

A. Al-Harrasi, I. Brüdgam, H. Hartl, H.-U. Reißig*
Crystal structure of 1R,5S,8R,9S-8-azidomethyl-2-benzyl-
6,6-dimethyl-3,7-dioxa-2-aza-bicyclo[3.3.1]nonan-9-0l, C16H22N4O3

Z. Kristallogr. NCS 2005, 220, 599 - 600.

A. Al-Harrasi, I. Brüdgam, H. Hartl, H.-U. Reißig*
Crystal structure of 3S,4S,5R,6S,7R-5-amino-6-(tert-butyldimethylsiloxy)-
7(tert-butyldimethylsiloxymethyl)-3-hydroxymethyl-2,2-dimethyloxepan-4-ol, C22H49NO5Si2
Z. Kristallogr. NCS 2006, 221, 131 – 132.

A. Al-Harrasi, H.-U. Reißig*
Enantiomerenreiner Kohlenhydratmimetika durch Lewis-Säure-induzierte Umlagerung von 1,3-dioxolanyl-substitutierten 3,6-Dihydro-2H-1,2-oxazinen
Angew. Chem. 2005, 117, 6383 - 6387.

A. Al-Harrasi, H.-U. Reißig*
Synthesis of Enantiopure Carbohydrate Mimetics by Lewis Acid Catalyzed Rearrangement of 1,3-Dioxolanyl-Substituted 1,2-Oxazines
Angew. Chem. Int. Ed. 2005, 44, 6227  –  6231.

A. Al-Harrasi, H.-U. Reißig*
Synthesis of Enantiopure Functionalized β-Alkoxy γ-Amino Aldehydes by a New Internal Redox Ring Cleavage of Carbohydrate Derived 1,2-Oxazines
Synlett 2005, 1152 – 1154.

R. Pulz, A. Al-Harrasi, H.-U. Reißig*
Acid Promoted Syntheses of New Enantiopure Amino Sugar Derivatives from 3,6-Dihydro-2H-1,2-oxazines
Synlett 2002, 817 – 819.

Direct link

 Publications 

J. Saadi, C. Bentz, K. Redies, D. Lentz, R. Zimmer, H.-U. Reißig*
Stereoselective Synthesis of Tricyclic Compounds by Intramolecular Palladium-Catalyzed Addition of Aryl Iodides to Carbonyl Groups
Beilstein J. Org. Chem. 2016, 12, 1236 – 1242.

D. Reich, D. S. Müller, L. Schefzig, R. Zimmer,* H.-U. Reißig*
One-Pot Generation of C≡X Bonds from Methyl 2-Siloxycyclopropanecarboxylates: Simple Syntheses of Functionalized Nitriles and Alkynes
Synlett 2014, 25, 2265 – 2270.

T. H. Ngo, H. Berndt, M. Wilsdorf, D. Lentz, H.-U. Reißig*
Linear and Cyclic Hybrids of Alternating Thiophene–Amino Acid Units: Synthesis and Effects of Chirality on Conformation and Molecular Packing
Chem. Eur. J. 2013,19, 15155 – 15165.

D.Gladow, H.-U. Reißig*
Alkylation and Ring Opening of Perfluoroalkyl- and Perfluoroaryl-Substituted 2-Siloxycyclopropanecarboxylates Yielding Fluorinated γ-Oxo Esters or β,γ-Unsaturated Ketones
Synthesis 2013, 2179 – 2187.

M. H. Beyzavi, C. Nietzold, H.-U. Reißig*, A. Wiehe*
Synthesis of Functionalized trans-A2B2-Porphyrins Using Donor-Acceptor Cyclopropane-Derived Dipyrromethanes
Adv. Synth. Catal. 2013, 355, 1409 – 1422.

M. H. Beyzavi, D. Lentz, H.-U. Reißig*, A. Wiehe*
Synthesis of New Functionalized Calix[n]phyrin Macrocycles with Varied Ring Sizes by Using a Sterically Congested Dipyrromethane
Chem. Eur. J. 2013, 19, 6203 – 6208.

M. H. Beyzavi, D. Lentz, H.-U. Reißig*, A. Wiehe*
Synthesis of Functionalized, Sterically Congested Calix[4]phyrin Macrocycles Using Donor-Acceptor-Substituted Cyclopropanes – First Example of a Mono-meso-spirolactone Incorporated into a Calix[4]phyrin
Eur. J. Org. Chem. 2013, 269 – 282.

T. H. Ngo, H. Berndt, D. Lentz, H.-U. Reißig*
Linear and Cyclic Amides with a Thiophene Backbone: Ultrasound-Promoted Synthesis and Crystal Structures
J. Org. Chem. 2012, 77, 9676 – 9683.

D. Gladow, H.-U. Reißig*
Synthesis of Perfluoroalkyl-Substituted γ-Lactones and 4,5-Dihydropyridazin-3(2H)-ones via Donor-Acceptor Cyclopropanes
Helv. Chim. Acta 2012, 95, 1818 – 1830.

H. A. Laub, D. Gladow, H.-U. Reißig*, H. Mayr*
The Influence of Perfluorinated Substitutents on the Nucleophilic Reactivities of Silyl Enol Ethers
Org. Lett. 2012, 14, 3990 – 3993.
H. Özbek, D. Lentz, H.-U. Reißig*
New Macrocyclic Peptidomimetics Containing 5-Aminothiophene Subunits
Eur. J. Org. Chem. 2010, 6319 – 6322.

H. Özbek, I. S. Veljkovic, H.-U. Reißig*
Gewald Synthesis of Aminothiophene Carboxylic Acids Providing New Dipeptide Analogues
Synlett 2008, 3145 – 3148.

I. Veljkovic, R. Zimmer, H.-U. Reißig*, I. Brüdgam, H. Hartl
A Flexible Three-Component Synthesis of Novel δ-Amino Acids Incorporating an Imidazo[1,2-α]pyridine Backbone
Synthesis 2006, 2677 - 2684.

R. Zimmer, A. Ziemer, M. Gruner, I. Brüdgam, H. Hartl, H.-U. Reißig*
Siloxycyclopropanes in Ugi Four-Component Reaction: A New Method for Synthesis of Highly Substituted Pyrrolidinone Derivatives
Synthesis 2001, 1649 - 1658.

 

Direct link

Publications 

•  M. Taszarek, H.-U. Reißig*
Heck Reactions and Carbonylations of Alkenyl Nonaflates – Synthesis of Tetradehydroamino Acids and α,β-Unsaturated Carboxylic Acids
ChemistrySelect 2016, 1, 5712 – 5715.

P. Hommes, H.-U. Reißig*
Synthesis of Highly Functionalized 2,2´-Bipyridines by Cyclocondensation of β-Ketoenamides – Scope and Limitations
Beilstein J. Org. Chem. 2016, 12, 1170 – 1177.

•   G. Podolan, L. Hettmanczyk, P. Hommes, B. Sarkar,* H.-U. Reißig*
Synthesis and (Spectro)electrochemistry of New Ferrocenyl-Substituted Pyridine Derivatives
Eur. J. Org. Chem. 2015, 7317 – 7323.

•  J. Högermeier, D. Trawny, R. Zimmer, H.-U. Reissig*
Diels-Alder Reactions of 1,3-Dienes Incorporated into 8-Oxa- and 8-Thia-bicyclo[3.2.1]octane Skeletons: A Convenient Access to Complex Tri- and Tetracyclic Compounds
Synthesis
2015, 47, 2767 – 2775.

•  D. Trawny, M. Quennet, N. Rades, D. Lentz, B. Paulus, H.-U. Reissig*
Syntheses, Structures and Conformational Dynamics of 1,3,5-Tris(3‘‘-ethynylbi-phenyl-2‘-yl)benzene Derivatives
Eur. J. Org. Chem. 2015, 4667 – 4674.

J. Dash, D. Trawny, J. P. Rabe, H.-U. Reissig*
C3-Symmetric Pyridine and Bipyridine Derivatives: Simple Preparation by Cyclocondensation and 2D Self-Assembly at a Solution-Graphite Interface
Synlett
2015, 26, 1486 – 1489.

•  D. Trawny, V. Kunz, H.-U. Reißig*
Modular Syntheses of Star-Shaped Pyridine, Bipyridine, and Terpyridine Derivatives by Employing Sonogashira Reactions
Eur. J. Org. Chem. 2014, 6295 – 6302.

•  D. Gladow, S. Doniz-Kettenmann, H.-U. Reißig*

1,3-Dipolar Cycloadditions of Ethyl 2-Diazo-3,3,3-trifluoropropanoate to Alkynes and [1,5] Sigmatropic Rearrangements of the Resulting 3H-Pyrazoles: Synthesis of Mono-, Bis- and Tris(trifluoromethyl)-Substituted Pyrazoles
Helv. Chim. Acta, 2014, 97, 808 – 821.

• 

D. Gladow, H.-U. Reißig*
Perfluoroalkyl-Substituted Thiophenes and Pyrroles from Donor-Acceptor Cyclopropanes and Heterocumulenes: Synthesis and Exploration of their Reactivity
J. Org. Chem. 2014, 79, 4492 – 4502.

L. Bouché, H.-U. Reißig*
Synthesis of Di- and Trivalent Carbohydrate Mimetics with Oxepane Substructure by Employing Copper-Catalyzed [3+2] Cycloadditions of Alkynes with Azidooxepanes
Eur. J. Org. Chem. 2014, 3697 – 3703.

M. Domínguez, H.-U. Reißig*
New 4-Pyridyl Nonaflates as Precursors for Push-Pull Solvatochromik Dyes
Synthesis 2014, 46, 1110 – 1106.

M. K. Bera, M. Domínguez, P. Hommes, H.-U. Reißig*
The Flögel-Three-Component Reaction with Dicarboxylic Acids - An Approach to Bis(β-alkoxy-β - ketoenamides) for the Synthesis of Complex Pyridine and Pyrimidine Derivatives
Beilstein J. Org. Chem. 2014, 10, 394 – 404.

M. K. Bera, S. L. Gholap, P. Hommes, K. Neuthe, D. Trawny, J. P. Rabe, D. Lentz, R. Zimmer, H.-U. Reißig*
Synthesis and Properties of Branched Oligo(2-thienyl)- and Oligo(2,2’-bithien-5-yl)-Substituted Pyridine Derivatives
Adv. Synth. Catal. 2013, 355, 3463 – 3474

P. Hommes, S. Berlin, H.-U. Reißig*
Trimethylsilyl Trifluoromethanesulfonate-Promoted Cyclocondensation of b-Keto-enamides and Subsequent Nonaflation to Pyrid-2-yl and Pyrid-4-yl Nonaflates as Flexible Precursors for Polysubstituted Pyridines
Synthesis 2013, 45, 3288 – 3294.

S. L. Gholap, P. Hommes, K. Neuthe, H.-U. Reißig*
Per(2-thienyl)pyridines: Synthesis and Properties
Org. Lett. 2013, 15, 318 – 321.

T. Lechel, G. Podolan, B. Brusilowskij, C. A. Schalley, H.-U. Reißig*
Unexpected One-Step Formation of Iodo[1,3]dioxolo[4,5-c]pyridine Derivatives by a Hofmann-Löffler-Freytag Reaction: Studies on the Synthesis of a Pyridine-Containing Macrocycle
Eur. J. Org. Chem. 2012, 5685 – 5692.

C. Eidamshaus, P. Hommes, H.-U. Reißig*
Palladium-Catalyzed Coupling of Pyrid-4-yl Nonaflates with Methyl Diazoacetate
Synlett 2012, 1670 – 1674.

C. Eidamshaus, T. Triemer, H.-U. Reißig*
Synthesis of 4-Quinolones via Cyclocondensation of Substituted ortho-Amidoacetophenones: A Refit to the Camps Cyclization by Applying Trimethylsilyl Trifluoromethanesulfonate/Triethylamine
Synthesis 2011, 3261 – 3266.

C. Eidamshaus, H.-U. Reißig*
A Chiral Pool Strategy for the Synthesis of Enantiopure Hydroxymethyl-Substituted Pyridine Derivatives
Eur. J. Org. Chem. 2011, 6056 – 6069

M. K. Bera, P. Hommes, H.-U. Reißig*
In Search of Oligo(2-thienyl)-Substituted Pyridine Derivatives: A Modular Approach to Di-, Tri- and Tetra(2-thienyl)pyridines
Chem. Eur. J. 2011, 17, 11838 – 11844.

P. Hommes, P. Jungk, H.-U. Reißig*
Four-Component Synthesis of Functionalized 2,2’-Bipyridines Based on the Blaise Reaction
Synlett 2011, 2311 – 2314.

T. Lechel, J. Dash, C. Eidamshaus, I. Brüdgam, D. Lentz, H.-U. Reißig*
A Three-component Synthesis of β-Alkoxy-β-keto-enamides - Flexible Precoursors for 4-Hydroxypyridine Derivatives and their Palladium-catalysed Reactions
Org. Biomol. Chem. 2010, 8, 3007 – 3014.

•  T. Lechel, I. Brüdgam, H.-U. Reißig*
Preparation of pyridine-3,4-diols, their crystal packing and their use as precursors for palladium-catalyzed cross-coupling reactions
Beilstein Journal of Organic Chemistry 2010, 6, No. 42.

J. Högermeier, H.-U. Reißig*
Nine Times Fluoride can be Good for your Syntheses. Not just Cheaper: Nonafluorobutanesulfonates as Intermediates for Transition Metal-Catalyzed Reactions
Adv. Synth. Catal. 2009, 351, 2747 – 2763.

J. Högermeier, H.-U. Reißig*
Mild and Efficient Sonogashira Couplings of 8-Oxa- and 8-Thiabicyclo[3.2.1]octanone Derived Alkenyl Nonaflates
Tetrahedron 2007, 63, 8485 – 8491.

J. Högermeier, H.-U. Reißig*
First Comprehensive Investigation of Suzuki Couplings of Alkenyl Nonaflates with Aryl and Alkenyl Boronic Acid Derivatives by Using Classical Conditions and Microwave Heating
Chem. Eur. J. 2007, 13, 2410 – 2420.

F. Aulenta, H.-U. Reißig*
Heck Reactions of Quinoline-Derived Nonaflates
Synlett 2006, 2993 - 2996.

J. Högermeier, H.-U. Reißig*
Suzuki Couplings of New Bicyclic Boronic Esters Derived from 8-Heterobicyclo[3.2.1]octenyl Nonaflates and Application to the Synthesis of an Epibatidine-Atropine Hybrid
Synlett 2006, 2759 - 2762.

J. Högermeier, H.-U. Reißig*, I. Brüdgam, H. Hartl
Nonaflates from 8-Oxabicyclo[3.2.1]oct-6-en-3-ones as Building Blocks for Diversity Orientated Synthesis: Preparation, Heck-Couplings and Subsequent Diels-Alder Reactions
Adv. Synth. Catal. 2004, 346, 1868 – 1879.

I. M. Lyapkalo, J. Högermeier, H.-U. Reißig*
Synthesis of New Tropinone Derivatives by Palladium-Catalyzed Couplings of 8-Azabicyclo[3.2.1]oct-2-enyl Nonaflates
Tetrahedron 2004, 60, 7721 - 7729.

I. M. Lyapkalo*, H. U. Reißig, A. Schäfer, A. Wagner
Study of Unusually High Rotation Barriers about S,N Bonds in Nonafluoro-1-butanesulfonamides: Electronic Nature of the Torsional Effect
Helv. Chim. Acta 2002, 85, 4206 – 4215.
 
I. M. Lyapkalo, M. Webel, H.-U. Reißig*
One-Pot Transformation of Silyl Enol Ethers into 1,3-Dienes: In Situ Generation of Alkenyl Nonaflates Followed by Heck Reactions – Scope and Limitations
Eur. J. Org. Chem. 2002, 3646 – 3658.

I. M. Lyapkalo, M. Webel, H.-U. Reißig*
An Expedient and Stereoselective Synthesis of Alkenyl Nonaflates from Silyl Enol Ethers: Optimization, Scope and Limitations
Eur. J. Org. Chem. 2002, 1015 - 1025.
 
I. M. Lyapkalo, M. Webel, H.-U. Reißig*
Synthesis and Heck Reactions of Ethenyl and (Z)-Butadien-1-yl Nonaflate Obtained by Fragmentation of Furan Derivatives
Eur. J. Org. Chem. 2001, 4189 – 4194.

I. M. Lyapkalo, M. Webel, H.-U. Reißig*
Enantioselective Synthesis of Cyclohexenylalkenes by Asymmetric Deprotonation of 4-tert-Butylcyclohexanone Followed by O-Nonaflation and Heck Couplings
Synlett 2001, 1293 – 1295.

R. Zimmer*, M. Webel, H.-U. Reißig
Nonafluoro-1-butanesulfonyl Fluoride: More than a Fluorinating Reagent
J. Prakt. Chem. 1998, 340, 274 – 277.
 
M. Webel, H.-U. Reißig*
Heck Reactions Starting from Silyl Enol Ethers - A Simple One-Pot Nonaflation-Coupling Procedure for the Synthesis of 1,3-Dienes
Synlett 1997, 1141 – 1142.
 
E. Hirsch, S. Hünig*, H.-U. Reißig
Darstellung von Enolsulfonsäureestern aus Trimethylsilylenolethern: Synthetische Konsequenz eines bemerkenswerten Kationeneffekts
Chem. Ber. 1982, 115, 3687 – 3696.
 
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