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 Publications 

  • H.-U. Reißig*, R. Zimmer
    Münchnone – 50 Jahre und ein bisschen weiser

    Angew. Chem.
    2014, 126, 9864 – 9866.

  • H.-U. Reißig*, R. Zimmer
    Münchnones – New Facets after 50 Years
    Angew. Chem. Int. Ed. 2014, 53, 9708 – 9710.

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

  • 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.

  • E. Schmidt, H.-U. Reißig*, R. Zimmer
    Regio- and Stereoselective 1,3-Dipolar Cycloadditions to 6H-1,2-Oxazines Leading to New Heterobicyclic Compounds
    Synthesis 2006, 2074 -2084

  • E. Schmidt, H.-U. Reißig, O. Rademacher*
    Crystal Structure of 3aS*,4S*,7aR*-4-Ethoxy-3a,7a-dihydro-3,7-diphenyl-
    4H-1,5-dioxa-2,6-diazaindene, C19H18N2O3

    Z. Kristallogr. NCS 2000, 215, 283 - 284.

  • R. Zschiesche, H.-U. Reißig*
    Reductive Transformations of Polyfunctional Nitro Compounds: Synthesis of Methyl 7-Aminoalkanoates and Five-Membered Cyclic Nitrones - Inter- and Intramolecular 1,3-Dipolar Cycloadditions
    Liebigs Ann. Chem. 1989, 551 - 557.

  • J. L. Flippen-Anderson, I. Karle, R. Huisgen*, H.-U. Reißig
    Trimerisierung eines Azomethin-imins durch drei aufeinanderfolgende 1,3-dipolare Cycloadditionen
    Angew. Chem. 1980, 92, 936 - 937.

  • J. L. Flippen-Anderson, I. Karle, R. Huisgen*, H.-U. Reißig
    Trimerization of an Azomethine Imine by Threee Successive 1,3-Dipolar Cycloaddition Reactions
    Angew. Chem. Int. Ed. Engl. 1980, 19, 906 - 907.

  • R. Huisgen*, H.-U. Reißig
    Cycloadditions to Methyl 3,3-Dimethyl-3H-pyrazole-5-carboxylate
    J. Chem. Soc., Chem. Commun. 1979, 568 - 570.

  • R. Huisgen*, H.-U. Reißig, H. Huber, S. Voss
    α-Diazocarbonyl Compounds and Enamines - A Dichotomy of Reaction Paths
    Tetrahedron Lett. 1979, 2987 - 2990.

  • H.-U. Reißig, R. Huisgen*
    Conducted Tour Mechanism of Ester Group Migration in a 3H-Pyrazole
    J. Am. Chem. Soc. 1979, 101, 3648 - 3649.

  • R. Huisgen*, H.-U. Reißig, H. Huber
    Diazocarbonyl Compounds and 1-Diethylaminopropyne
    J. Am. Chem. Soc. 1979, 101, 3647 - 3648.
  • W. Bihlmaier, R. Huisgen*, H.-U. Reißig, S. Voss
    Reactivity Sequences of Dipolarophiles Towards Diazocarbonyl Compounds - MO Pertubation Treatment
    Tetrahedron Lett. 1979, 2621 - 2624.

  • R. Huisgen*, W. Bihlmaier, H.-U. Reißig
    Azokupplung von α-Diazocarbonylverbindungen mit N-(1-Cyclopentenyl)aminen
    Angew. Chem. 1979, 91, 347 - 348.

  • R. Huisgen*, W. Bihlmaier, H.-U. Reißig
    Azo Coupling of a-Diazo Cyrbonyl Compounds with N-(1-Cyclopentenyl)amines
    Angew. Chem. Int. Ed. Engl. 1979, 18, 331 - 332.

  • R. Huisgen*, H.-U. Reißig
    Cycloadditionen von α-Diazocarbonylverbindungen an Enamine
    Angew. Chem. 1979, 91, 346 - 347.

  • R. Huisgen*, H.-U. Reißig
    Cycloadditions of a-Diazo Carbonyl Compounds to Enamines
    Angew. Chem. Int. Ed. Engl. 1979, 18, 330 - 331.

  • J. Geittner, R. Huisgen*, H.-U. Reißig
    Solvent Dependence of Cycloaddition Rates of Phenyldiazomethane and Activation Parameters
    Heterocycles (Sendai) 1978, 11, 109 - 112.

  • L. Fisera, J. Geittner, R. Huisgen*, H.-U. Reißig
    Cycloaddition Rates of Diazomethane and Diphenyldiazomethane
    Heterocycles (Sendai) 1978, 10, 153 - 158.

  • W. Bihlmaier, J. Geittner, R. Huisgen*, H.-U. Reißig
    The Stereospecificity of Diazomethane Cycloadditions
    Heterocycles (Sendai) 1978, 10, 147 - 152.

 

Direct link

Publications

  • H. Angert, R. Czerwonka, H.-U. Reißig*
    Mukaiyama Reactions of a Silyl Enol Ether with Heteroatom-Substituted β-Formyl Esters
    Liebigs Ann./Recueil 1997, 2215 - 2220.

  • H. Angert, R. Czerwonka, H.-U. Reißig*
    TiCl4 and LiClO4 Promoted Additions of O-Silylketene Acetals to Chiral β-Formyl Esters
    J. Prakt. Chem. 1997, 339, 453 - 455.

  • H. Angert, R. Schumacher, S. Foro, H.-U. Reißig, H. J. Lindner*
    Crystal Structure of 4,5-Dihydro-4,4-dimethyl-5-(4,4-dimethyl-3-oxo-2-pentyl)-
    2(3H)-furanone, OCOCH2C(CH3)2CHCH(CH3)COC(CH3)3

    Z. Kristallogr. 1996, 211, 403 - 404.

  • H. Angert, R. Schumacher, S. Foro, H.-U. Reißig, H. J. Lindner*
    Crystal Structure of 4,5-Dihydro-5-(4,4-dimethyl-3-oxo-2-pentyl)-2(3H)-furanone, OCO(CH2)2CHCH(CH3)COC(CH3)3
    Z. Kristallogr. 1996, 211, 401 - 402.

  • H. Angert, R. Schumacher, H.-U. Reißig*
    Chelate-Controlled Additions of Titanium and Lithium Enolates to Chiral β-Formyl Esters - Diastereofacial and Simple Diastereoselectivity
    Chem. Ber. 1996, 129, 227 - 232.

  • 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.

  • H.-U. Reißig*, H. Angert, T. Kunz, A. Janowitz, G. Handke, E. Bruce-Adjei
    Ester Groups as Effective Ligands in Chelate-Controlled Additions of Cuprates and Grignard Reagents to Chiral β-Formyl Esters
    J. Org. Chem. 1993, 58, 6280 - 6285.

  • H. Angert, T. Kunz, H.-U. Reißig*
    Chelate-Controlled Mukaiyama Reactions with Chiral β-Formyl Esters
    in Tetrahedron-Symposium-in-Print on Organotitanium Reagents in Organic Synthesis (M. T. Reetz, Ed.)
    Tetrahedron 1992, 48, 5681 - 5690.

  • T. Kunz, A. Janowitz, H.-U. Reißig*
    A Chelate-Controlled Route to Disubstituted and Tetrasubstituted γ-Lactones - Stereoselectivity in Lewis Acid Promoted Additions to Chiral Methyl β-Formylcarboxylates
    Chem. Ber. 1989, 122, 2165 - 2175.

  • A. Janowitz, T. Kunz, G. Handke, H.-U. Reißig*
    Asymmetric 1,2- and 1,3-Inductions and Solvent Dependence Found in Chelate-Controlled Additions of Grignard Reagents and Cuprates to Chiral β-Formyl Esters – Stereoselective Synthesis of γ-Lactones
    Synlett 1989, 24 – 25.

  • T. Kunz, H.-U. Reißig*
    Radical Additions in Aqueous Medium: Direct Synthesis of 5-Allyl-Substituted γ-Lactones from Allylic Bromides/Zinc and Methyl γ-Oxocarboxylates
    Liebigs Ann. Chem. 1989, 891 - 893.

  • T. Kunz, H.-U. Reißig*
    Ein neuer Weg zu trans-substituierten γ-Lactonen
    Angew. Chem. 1988, 100, 297 - 298.

  • T. Kunz, H.-U. Reißig*
    A New Route to trans-Substituted γ-Lactones
    Angew. Chem. Int. Ed. Engl. 1988, 27, 268 - 270.

Direct link

Publications

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

  • H.-U. Reißig*, G. Böttcher, R. Zimmer
    New 1,3-Dihydroazepin-2-one Derivatives by [3,3]-Sigmatropic Rearrangement of Suitably Substituted 2-Alkenylcyclopropyl Isocyanates
    Can. J. Chem 2004, 82, 166 – 176.

  • H.-U. Reißig*, R. Zimmer
    Donor-Acceptor-Substituted Cyclopropane Derivatives and their Application in Organic Synthesis
    Chem. Rev. 2003, 103, 1151 – 1196.

  • P. K. Patra, H.-U. Reißig*
    Functionalized Azamacrocycles and Large-Ring α-Amino Esters by One-Pot Syntheses from Methyl 2-Siloxy-2-vinylcyclopropanecarboxylates
    Eur. J. Org. Chem. 2001, 4195 – 4206.

  • 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.

  • P. K. Patra, H..U. Reißig*
    An Efficient One-pot Synthesis of Functionalized Azamacrocycles from Methyl 2-Siloxy-2-vinylcyclopropanecarboxylates
    Synlett 2001, 33 – 36.

  • F. A. Khan, R. Czerwonka, H.-U. Reißig*
    Pd-Catalyzed Reactions of Donor-Acceptor Substituted Cyclopropanes and their Ring-opened Derivatives: Attempted Heck Cyclization and Novel One-pot Enolate Arylations
    Eur. J. Org. Chem. 2000, 3607 - 3617.

  • G. Böttcher, H.-U. Reißig*
    Synthesis of New Highly Substituted 1,3-Dihydroazepin-2-ones Starting from 2-Siloxycyclopropanecarboxylates
    Synlett 2000, 725 - 727.

  • D. Sperling, H.-U. Reißig, J. Fabian*
    1,3-Sigmatropic Rearrangements of Divinylcyclopropane Derivatives and Hetero Analogs in Competition with Cope-Type Rearrangements - A DFT Study
    Eur. J. Org. Chem. 1999, 1107 - 1114.

  • A. Ullmann, M. Gruner, H.-U. Reißig*
    Synthesis of Functionalized Cyclophanes by Ring-Opening/Ring-Closure Cascade Reactions of Siloxycyclopropanes
    Chem. Eur. J. 1999, 5, 187 – 197.

  • A. Ullmann, H.-U. Reißig*, O. Rademacher
    A Repetitive Approach to the Synthesis of Medium and Large Ring Compounds with a Ring-Opening/Ring-Closure Cascade Reaction of Siloxycyclopropane Derivatives as Crucial Step
    Eur. J. Org. Chem. 1998, 2541 – 2549.

  • D. Sperling, H.-U. Reißig, J. Fabian*
    A DFT Study on the Vinylcyclopropanecarbaldehyde to 2,5-Dihydrooxepin Hetero-Cope-type Rearrangement and on Related Reactions
    Liebigs Ann./Recueil 1997, 2443 - 2450.

  • H.-U. Reißig*, R. Schumacher, D. Ferse
    Baeyer-Villiger Oxidations of γ-Oxo Esters - Determination of the Absolute Configurations of Methyl 2-Siloxycyclopropanecarboxylates - Interpretation of the Enantioselective Cyclopropanations of Silyl Enol Ethers
    Liebigs Ann./Recueil 1997, 2119 - 2124.

  • D. Sperling, H.-U. Reißig, J. Fabian*
    Quantenchemische Berechnungen zur chemischen Reaktivität: Isomerisierung einiger substituierter Cyclopropane
    Wiss. Z. Techn. Univ. Dresden 1997, 46, (Heft 5) 33 - 38.

  • R. Schumacher, F. Dammast, H.-U. Reißig*
    Screening of Various Catalysts for the Asymmetric Cyclopropanation of Structurally Typical Silyl Enol Ethers - Scope and Limitations of Evans's Bisoxazoline Copper Catalyst
    Chem. Eur. J. 1997, 3, 614 - 619.

  • R. Schumacher, H.-U. Reißig*
    Influence of Nucleophilicity of Silyl Enol Ethers on Stereoselectivities in Asymmetric Cyclopropanation Reactions
    Liebigs Ann./Recueil 1997, 521 - 526.

  • R. Schumacher, H.-U. Reißig*
    Stereoselective Cyclopropanation of Chiral Carbohydrate-Derived Enol Ethers
    Synlett 1996, 1121 - 1122.

  • M. Buchert, H.-U. Reißig*
    Rearrangement of Donor-Acceptor-Substituted Vinylcyclopropanes to Functionalized Cyclopentene Derivatives: Evidence for Zwitterionic Intermediates
    Liebigs Ann. 1996, 2007 - 2013.

  • F. A. Khan, R. Czerwonka, H.-U. Reißig*
    A Novel Pd(0)-Catalyzed One-Pot Transformation of Substituted Siloxycyclopropanes to Indane Derivatives
    Synlett 1996, 533 - 535.

  • J. Schnaubelt, E. Marks, H.-U. Reißig*
    [4+1] Cycloadditions of the Rhodium Di(methoxycarbonyl) Carbenoid to 2-Siloxy-1,3-dienes
    Chem. Ber. 1996, 129, 73 - 75.

  • J. Schnaubelt, A. Ullmann, H.-U. Reißig*
    An Efficient One-Pot Synthesis of Functionalized Cyclodecenone Derivatives from Siloxycyclopropanes
    Synlett 1995, 1223 – 1225.

  • J. Schnaubelt, H.-U. Reißig*
    Chelate Controlled Intramolecular Diels-Alder Reaction as Key for Synthesis of a Dihydromevinolin Precursor
    Synlett 1995, 452 - 454.

  • B. Hofmann, H.-U. Reißig*
    Characteristic Reactions of 4-Siloxy-2,5-dihydrooxepines: Desilylation, [2+2] and [4+2] Cycloadditions
    Chem. Ber. 1994, 127, 2337 - 2339.

  • B. Hofmann, H.-U. Reißig*
    Swern Oxidation of Alkenyl-Substituted 2-(tert-Butyldimethylsiloxy)-1-
    (hydroxymethyl)-cyclopropanes: A Novel and Flexible Route to Functionalized 2,5-Dihydrooxepines

    Chem. Ber. 1994, 127, 2327 - 2335.

  • B. Hofmann, H.-U. Reißig*
    Synthesis of New Alkenyl-Substituted 2-(tert-Butyldimethylsiloxy)cyclopropane-
    carboxylates and their Diastereoselective Conversion into (Hydroxymethyl)-
    cyclopropanes

    Chem. Ber. 1994, 127, 2315 - 2325.

  • 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.

  • F. Dammast, H.-U. Reißig*
    Synthese optisch aktiver 2-Siloxycyclopropancarbonsäureester durch asymmetrische Katalyse II. Einfluß der Silylenoletherstruktur auf die enantioselektive Cyclopropanierung mit Diazoessigsäuremethylester
    Chem. Ber. 1993,126, 2727 - 2732.

  • F. Dammast, H.-U. Reißig*
    Synthese optisch aktiver 2-Siloxycyclopropancarbonsäureester durch asymmetrische Katalyse I. Katalysatoreinfluß auf die Cyclopropanierung von (Z)-1-Phenyl-1-(trimethylsiloxy)prop-1-en
    Chem. Ber. 1993, 126, 2449 - 2456.

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

  • B. Hofmann, H.-U. Reißig*
    Synthesis of Functionalized 2,5-Dihydrooxepines by [3,3]-Sigmatropic Rearrangement of Cyclopropane Derivatives
    Synlett 1993, 27 - 29.

  • H.-U. Reißig*, I. Reichelt, T. Kunz
    Methoxycarbonylmethylation of Aldehydes Via Siloxycyclopropanes: Methyl 3,3-Dimethyl-4-oxobutanoate
    Org. Synth. 1992, 71, 189 - 199.

  • K. Paulini, H.-U. Reißig*
    Ein effektiver Weg zu GABA-analogen Aminosäuren: Cyclopropanierung von N-silylierten Allylaminen und Enaminen
    Liebigs Ann. Chem. 1991, 455 – 461.

  • H.-E. Radunz*, H.-U. Reißig, G. Schneider, A. Riethmüller
    Synthese enantiomerenreiner γ-Keto-δ-aminosäuren, zentrale Bausteine vieler Enzyminhibitoren
    Liebigs Ann. Chem. 1990, 705 - 707.

  • T. Kunz, A. Janowitz, H.-U. Reißig*
    Eine flexible Synthese von 4-Oxobutansäuremethylestern und deren Derivaten
    Synthesis 1990, 43 - 47.

  • Patent:
    H.-E. Radunz, H.-U. Reißig
    Verfahren zur enantioselektiven Herstellung von γ-Keto-δ-aminosäurederivaten,
    Deutsches Patentamt (P 3919898 vom 19.6.1989)

  • R. Zschiesche, H.-U. Reißig*
    Reductive Transformations of Polyfunctional Nitro Compounds: Synthesis of Methyl 7-Aminoalkanoates and Five-Membered Cyclic Nitrones - Inter- and Intramolecular 1,3-Dipolar Cycloadditions
    Liebigs Ann. Chem. 1989, 551 - 557.

  • H.-U. Reißig*, H. Holzinger, G. Glomsda
    A Titanoxycyclopropane as Intermediate in a Highly Stereoselective Homoaldol Type Addition - Syntheses of cis-Substituted Tetrahydrofuran Derivatives
    Tetrahedron-Symposium-in-Print on Strain-Assisted Synthesis (L. Ghosez, Ed.), Tetrahedron 1989, 45, 3139 - 3150.

  • T. Kunz, H.-U. Reißig*
    Enantioselective Synthesis of Siloxycyclopropanes and of γ-Oxocarboxylates by Asymmetric Catalysis
    Tetrahedron Lett. 1989, 30, 2079 - 2082.

  • H.-U. Reißig*, R. Zschiesche, A. Wienand, M. Buchert
    Synthesis with Donor-Acceptor-Substituted Vinylcyclopropanes
    in "Strain and Its Implications in Organic Chemistry" (A. de Meijere, S. Blechert, Eds.), S. 51 - 58, Kluwer Academic Publishers, Dordrecht 1989.

  • 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*
    Efficient Syntheses of Polyfunctional Nitro Compounds Using 2-Alkenyl-Substituted Methyl 2-Siloxycyclopropanecarboxylates as Key Building Blocks
    Liebigs Ann. Chem. 1988, 1165 - 1168.

  • C. Brückner, H. Holzinger, H.-U. Reißig*
    Diastereoselective Syntheses of Highly Substituted Methyl Tetrahydrofuran-3-carboxylates by Reactions of γ-Lactols with Silylated Nucleophiles
    J. Org. Chem. 1988, 53, 2450 – 2456.

  • C. Brückner, H.-U. Reißig*
    Efficient and Flexible Syntheses of Paraconic Esters and Other Highly Substituted Furanone Derivatives from Methyl 2-Siloxycyclopropanecarboxylates
    J. Org. Chem. 1988, 53, 2440 - 2450.

  • C. Brückner, B. Suchland, H.-U. Reißig*
    Eine neue Synthese von Pyrrolderivaten
    Liebigs Ann. Chem. 1988, 471 - 473.

  • C. Brückner, H.-U. Reißig*
    Thiophenderivate aus 2-Siloxycyclopropancarbonsäureestern durch neuartige 1,3- und 1,2-sigmatrope Umlagerungen
    Liebigs Ann. Chem. 1988, 465 - 470.

  • H.-U. Reißig
    Donor-Acceptor-Substituted Cyclopropanes: Versatile Building Blocks in Organic Synthesis
    Top. Curr. Chem. 1988, 144, 73 - 135.

  • R. Zschiesche, H.-U. Reißig*
    An Efficient Synthesis of 5-Membered Cyclic Nitrones from γ-Nitro Ketones
    Tetrahedron Lett. 1988, 29, 1685 - 1686.

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

  • C. Brückner, H.-U. Reißig*
    Geschwindigkeit und Regioselektivität der Hydrogenolyse einiger phenylsubstituierter Cyclopropane
    Chem. Ber. 1987, 120, 627 - 629.

  • C. Brückner, H.-U. Reißig*
    Katalytische Hydrogenolyse von 2-Siloxycyclopropancarbonsäureestern: Untersuchungen zu Chemo-, Regio- und Stereoselektivität
    Chem. Ber. 1987, 120, 617 - 626.

  • W. Bretsch, H.-U. Reißig*
    Synthese von β,γ-ungesättigten Ketonen und γ-Hydroxycarbonylverbindungen aus 2-Siloxycyclopropancarbonsäuremethylestern
    Liebigs Ann. Chem. 1987, 175 - 178.

  • R. Zschiesche, E. L. Grimm, H.-U. Reißig*
    Intramolekulare Diels-Alder-Reaktionen mit 2-Trimethylsiloxy-2-vinylcyclopropancarbonsäureestern als Schlüsselbausteinen
    Angew. Chem. 1986, 98, 1104 - 1105; Angew. Chem. Int. Ed. Engl. 1986, 25, 1086 - 1087.

  • H.-U. Reißig*, I. Reichelt, H. Lorey
    C-C-Verknüpfung durch Lewis-Säure-induzierte Cyclopropanringspaltung - Neue Wege zu hochsubstituierten Furan(on)derivaten
    Liebigs Ann. Chem. 1986, 1924 - 1939.

  • H.-U. Reißig*, H. Lorey
    Selenylierung, Sulfenylierung und Aminomethylierung von 2-Siloxycyclopropancarbonsäureestern durch Lewis-Säure-induzierte Ringöffnung
    Liebigs Ann. Chem. 1986, 1914 - 1923.

  • C. Brückner, H. Lorey, H.-U. Reißig*
    Diastereoselektive Synthese funktionalisierter Tetrahydrofuran-Derivate aus γ-Lactolen
    Angew. Chem. 1986, 98, 559 – 560.

  • C. Brückner, H. Lorey, H.-U. Reißig*
    Diastereoselektive Synthesis of Funktionalized Tetrahydrofuran Derivates from γ-Lactols
    Angew. Chem. Int. Ed. Engl. 1986, 25, 556 - 557.

  • H.-U. Reißig*, H. Lorey
    Lewis Acid promoted Additions of Cyclopropanes to Iminium Salts: A New Possibility for α-Methylene-γ-butyrolactone Synthesis
    J. Chem. Soc., Chem. Commun. 1986, 269 - 271.

  • E. L. Grimm, R. Zschiesche, H.-U. Reißig*
    2-Alkenyl-Substituted Methyl 2-Siloxycyclopropanecarboxylates as Masked Vinyl Ketones: Efficient Syntheses of Highly Functionalized Michael Adducts
    J. Org. Chem. 1985, 50, 5543 - 5545.

  • C. Brückner, H.-U. Reißig*
    Synthesis of Functionalized Furan Derivatives by Hydroxyalkylation of Methyl 2-Siloxycyclopropanecarboxylates
    J. Chem. Soc., Chem. Commun. 1985, 1512 - 1513.

  • H.-U. Reißig
    A Novel Rearrangement Leading to Methoxycarbonylmethylated Silyl Enol Ethers
    Tetrahedron Lett. 1985, 26, 3943 - 3946.

  • C. Brückner, H.-U. Reißig*
    Thiophenderivate durch neue Umlagerungen siloxysubstituierter Cyclopropancarbonsäureester
    Angew. Chem. 1985, 97, 578 - 579.

  • C. Brückner, H.-U. Reißig*
    Thiophene Derivatives by Novel Rearrangements of Siloxy-substituted Cyclopropanecarboxylates
    Angew. Chem. Int. Ed. Engl. 1985, 24, 588 - 589.

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

  • E. L. Grimm, H.-U. Reißig*
    2-Siloxy-Substituted Methyl Cyclopropanecarboxylates as Building Blocks in Synthesis: Efficient One-Pot Conversion to γ-Butyrolactones
    J. Org. Chem. 1985, 50, 242 - 244.

  • H.-U. Reißig*, I. Reichelt
    Ring Cleaving Selenenylation and Sulfenylation of Cyclopropane Derivatives Promoted by TiCl4
    Tetrahedron Lett. 1984, 25, 5879 - 5880.

  • I. Reichelt, H.-U. Reißig*
    Eine einfache und flexible Synthese für 4,5-Dihydro-2H-3-pyridazinone
    Synthesis 1984, 786 - 787.

  • I. Reichelt, H.-U. Reißig*
    Zur Ringöffnung von 2-(Trimethylsilylmethyl)cyclopropancarbonsäuremethylester
    Liebigs Ann. Chem. 1984, 828 - 830.

  • I. Reichelt, H.-U. Reißig*
    Flexible und effektive Synthese für 4-Oxo-2-alkensäuremethylester
    Liebigs Ann. Chem. 1984, 820 - 827.

  • E. Kunkel, I. Reichelt, H.-U. Reißig*
    Ringöffnungsreaktionen von 2-Siloxycyclopropancarbonsäuremethylestern zu 4-Oxoalkansäurederivaten
    Liebigs Ann. Chem. 1984, 802 - 819.

  • I. Reichelt, H.-U. Reißig*
    Deprotonierung und diastereoselektive Alkylierung von 2-siloxysubstituierten Cyclopropancarbonsäuremethylestern
    Liebigs Ann. Chem. 1984, 531 - 551.

  • E. Kunkel, I. Reichelt, H.-U. Reißig*
    Synthese von 2-siloxysubstituierten Cyclopropancarbonsäuremethylestern
    Liebigs Ann. Chem. 1984, 512 - 530.

  • I. Reichelt, H.-U. Reißig
    Deprotonierung und diastereoselektive Alkylierung von Cyclopropancarbonsäuremethylestern
    Chem. Ber. 1983, 116, 3895 - 3914.

  • H.-U. Reißig*, I. Böhm
    Low Temperature Equilibration of Cyclopropanes by Lewis Acid Catalysis
    Tetrahedron Lett. 1983, 24, 715 - 718.

  • I. Böhm, R. Schulz, H.-U. Reißig*
    An Efficient and Highly Flexible Synthesis of α,β-Unsaturated γ-Oxoesters
    Tetrahedron Lett. 1982, 23, 2013 - 2016.

  • H.-U. Reißig*, I. Böhm
    High Diastereoselection in the Alkylation of Siloxy-Substituted Methyl Cyclopropanecarboxylates - Consequence of a Pyramidal Ester Enolate Anion?
    J. Am. Chem. Soc. 1982, 104, 1735 - 1737.

  • H.-U. Reißig
    Lewis-Acid-Promoted Additions of Carbonyl Compounds to Donor-Acceptor Substituted Cyclopropanes: A New Synthesis of 2,3-Dihydrofuran Derivatives
    Tetrahedron Lett. 1981, 22, 2981 - 2984.

  • I. Böhm, E. Hirsch, H.-U. Reißig*
    Alkylierung von Donor-Acceptor-substituierten Cyclopropanen: ein flexibler Weg zu 4-Oxocarbonsäureestern
    Angew. Chem. 1981, 93, 593 - 594.

  • I. Böhm, E. Hirsch, H.-U. Reißig*
    Alkylation of Donor-Acceptor Substituted Cyclopropanes: A Flexible Route to 4-Oxocarboxylic Acid Esters
    Angew. Chem. Int. Ed. Engl. 1981, 20, 574.

  • H.-U. Reißig*, E. Hirsch
    Donor-acceptor-substituierte Cyclopropane: Synthese und Ringöffnung zu 1,4-Di-carbonylverbindungen
    Angew. Chem. 1980, 92, 839 - 840.

  • H.-U. Reißig*, E. Hirsch
    Donor-Acceptor-Substituted Cyclopropanes: Synthesis und Ring Opening to 1,4-Dicarbonyl Compounds
    Angew. Chem. Int. Ed. Engl. 1980, 19, 813 - 814.

Direct link

Publications

  • M. Hoffmann, M. Buchert, H.-U. Reißig*
    Reactions of Fischer Carbene Complexes with Siloxydienes: Formation of Cycloheptadiene and Cyclopentene Derivatives - Formal [2+1] Cycloaddition Followed by Cope Rearrangement Versus Formal [3+2] Cycloaddition with or without Preceding Carbene-Ligand Metathesis
    Chem. Eur. J. 1999, 5, 876 - 882.

  • M. Hoffmann, M. Buchert, H.-U. Reißig*
    Weitere Überraschungen mit Fischer-Carbenkomplexen: formale [3+2]-Cycloadditionen mit und ohne vorgeschalteter Carbenligandmetathese
    Angew. Chem. 1997, 109, 281 - 283.

  • M. Hoffmann, M. Buchert, H.-U. Reißig*
    New Surprises with Fischer Carbene Complexes: Formal [3+2]Cycloadditions with and without Preceding Carabene-Ligand Metathesis

    Angew.
    Chem. Int. Ed. 1997, 36, 283 – 285.
  • M. Buchert, H.-U. Reißig*
    Rearrangement of Donor-Acceptor-Substituted Vinylcyclopropanes to Functionalized Cyclopentene Derivatives: Evidence for Zwitterionic Intermediates
    Liebigs Ann. 1996, 2007 - 2013.

  • M. Hoffmann, H.-U. Reißig*
    A Unique Solvent Effect Governing Periselectivity of the Carbene Transfer from Fischer Carbene Complexes: Mechanism, Scope and Limitation of Their Formal [3+2] Cycloaddition to Electron-Deficient Olefins
    Synlett 1995, 625 - 627.

  • M. Buchert, M. Hoffmann, H.-U. Reißig*
    On the Regioselectivity and Stereoselectivity of the Carbene Transfer from Fischer Carbene Complexes to Trisubstituted Electron-Deficient 1,3-Dienes
    Chem. Ber. 1995, 128, 605 - 614.

  • M. Buchert, H.-U. Reißig*
    Highly Functionalized Vinylcyclopropane Derivatives by Regioselective and Stereoselective Reactions of Fischer Carbene Complexes with 1,4-Disubstituted Electron-Deficient 1,3-Dienes
    Chem. Ber. 1992, 125, 2723 - 2729.

  • A. Wienand, H.-U. Reißig*, H. Fischer*, D. Pflumm, C. Troll
    Synthese und Kristallstrukturanalyse von Alkinylcarbenkomplexverbrückten Dicobalthexacarbonylkomplexen
    J. Organomet. Chem. 1992, 427, C9 - C14.

  • A. Wienand, H.-U. Reißig*
    Zur Bildung von Vinylcyclopropan- und Cyclopentenderivaten aus alkenylsubstituierten Chromcarben-Komplexen: Konkurrenz von formalen [2+1]- und [3+2]-Cycloadditionen
    Chem. Ber. 1991, 124, 957 - 965.

  • A. Wienand, H.-U. Reißig*
    Reactions of Fischer Carbene Complexes with Electron-Deficient Olefins: Scope and Limitations of This Route to Donor-Acceptor-Substituted Cyclopropanes
    Organometallics 1990, 9, 3133 - 3142.

  • A. Wienand, H.-U. Reißig*
    Stereospezifische Insertion des Carbenliganden eines Fischer-Carbenkomplexes in olefinische C-H-Bindungen
    Angew. Chem. 1990, 102, 1156 - 1157.

  • A. Wienand, H.-U. Reißig*

    Stereospezific Insertion of the Carbene Ligand of a Fischer Carbene Complex into Olefinic C–H Bonds
    Angew. Chem. Int. Ed. Engl.1990, 29, 1129 - 1131.

  • A. Wienand, H.-U. Reißig*, H. Fischer, J. Hofmann
    Eine einfache Synthese neuartiger alkenylsubstituierter Chromcarben-Komplexe
    Chem. Ber. 1989, 122, 1589 - 1592.

  • H.-U. Reißig
    Donor-Acceptor-Substituted Cyclopropanes via Fischer Carbene Complexes
    in "Organometallics in Organic Synthesis" (H. Werner, G. Erker, Eds.), S. 311 - 322, Springer, Heidelberg 1989.

  • A. Wienand, M. Buchert, B. Hofmann, H.-U. Reißig*
    The Carbene Complex Route to Donor-Acceptor-Substituted Cyclopropanes
    in "Advances in Metal Carbene Chemistry" (U. Schubert, Ed.) S. 271 - 273, Kluwer Academic Publishers, Dordrecht 1989.

  • M. Buchert, H.-U. Reißig*
    Regioselective and Stereoselective Synthesis of Vinylcyclopropane Derivatives from 1,3-Dienes and a Fischer Carbene Complex
    Tetrahedron Lett. 1988, 29, 2319 - 2320.

  • A. Wienand, H.-U. Reißig*
    The Carbene Complex Route to Donor-Acceptor-Substituted Cyclopropanes
    Tetrahedron Lett. 1988, 29, 2315 - 2318.
Direct link

Publications

  • M. S. Andrä, J. Thiemermann, J. Schnaubelt, D. Lentz, R. Zimmer, H.-U. Reißig*
    TADDOL-Promoted Enantioselective Intramolecular Diels-Alder Reactions of 1,7,9-Decatrien-3-ones to Octalin Derivatives
    Eur. J. Org. Chem. 2017, 124 – 130.

  • J. Thiemermann, J. Schnaubelt, R. Zimmer, H.-U. Reißig*
    Diastereoselective Diels-Alder Reactions of 1,7,9-Decatrien-3-ones to Highly Substituted Octalin Derivatives
    Synthesis 2016, 48, 5712 – 5715.

  • J. Thiemermann, M. S. Andrä, J. Schnaubelt, D. Lentz, R. Zimmer, H.-U. Reißig*
    A Modular Four-Component Route to Substituted 1,7,9-Decatrien-3-ones Using a Chloro-Substituted Phosphorane as Key C3 Building Block
    Synthesis 2016, 48, 4081 – 4090.

  • B. Frey, H.-U. Reißig*
    Facile Synthesis of an Octahydrobenzocycloheptenone Derivative Utilising Intramolecular Diels-Alder Reaction
    J. Prakt. Chem. 1999, 341, 173 - 178.

  • 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.

  • B. Frey, J. Schnaubelt, H.-U. Reißig*
    Variable Stereocontrol in Cycloadditions of 1,7,9-Decatrien-3-ones by Different Lewis Acidic Promoters - Application to a Short Synthesis of α-Eudesmol
    Eur. J. Org. Chem. 1999, 1385 - 1393.

  • B. Frey, J. Schnaubelt, H.-U. Reißig*
    Studies on the Synthesis of Natural Products with Bicyclo[4.4.0]decene Skeleton: Synthesis and Uncatalysed Intramolecular Diels-Alder Reactions of the Decatrienone Substrates
    Eur. J. Org Chem. 1999, 1377 - 1384.

  • J. Schnaubelt, H.-U. Reißig*
    Chelate Controlled Intramolecular Diels-Alder Reaction as Key for Synthesis of a Dihydromevinolin Precursor
    Synlett 1995, 452 - 454.

  • B. Frey, S. Hünig*, M. Koch, H.-U. Reißig*
    Seven-Membered Ring Chelates as a Tool for Stereocontrol in Intramolecular Diels-Alder Reactions: Application to a Short Synthesis of α-Eudesmol
    Synlett 1991, 854 - 856.

  • R. Zschiesche, B. Frey, E. Grimm, H.-U. Reißig*
    Zur Stereoselektivität der intramolekularen Diels-Alder-Reaktionen von 1,7,9-Decatrien-3-onen zu Octalonderivaten
    Chem. Ber. 1990, 123, 363 - 374.

  • R. Zschiesche, E. L. Grimm, H.-U. Reißig*
    Intramolekulare Diels-Alder-Reaktionen mit 2-Trimethylsiloxy-2-vinylcyclopropancarbonsäureestern als Schlüsselbausteinen
    Angew. Chem. 1986, 98, 1104 - 1105.

  • R. Zschiesche, E. L. Grimm, H.-U. Reißig*
    Intramolecular Diels-Alder-Reactions with Methyl 2-Trimethylsiloxy-2-vinylcyclopropanecarboxylates as Key Building Blocks
    Angew. Chem. Int. Ed. Engl. 1986, 25, 1086 - 1087.
Direct link

Publications

  • K. Paulini, H.-U. Reißig*, P. Rademacher
    On the Reactivity of N,N-Bis(trimethyl)silylated Enamines: Model Studies on Hetero Diels-Alder Reactions and Other Cycloadditions
    J. Prakt. Chem. 1995, 337, 209 - 215.

  • K. Paulini, A. Gerold, H.-U. Reißig*
    Reactions of 6-[Bis(trimethylsilyl)amino]-5,6-dihydro-4H-1,2-oxazines
    Liebigs Ann. 1995, 667 - 671.

  • 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, J. Richter, H. J. Lindner*, H. Paulus
    Crystal Structure of c-6-[N,N-Bis(trimethylsilyl)amino]-5,6-dihydro-
    r-4-[(1'-hydroxy-1'-methyl)ethyl]-t-5-methyl-3-phenyl-4H-1,2-oxazine,
    ONC(CH)(CH)(CH)(C6H5)-C(OH)(CH3)2(CH3)NSi(CH3)3Si(CH3)3

    Z. Kristallogr. 1994, 209, 900 - 901.

  • 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.

  • K. Paulini, H.-U. Reißig*
    Diastereoselective Radical Bromination of 5,6-Dihydro-4H-1,2-oxazines and Subsequent Substitution Reactions with Nitrogen Nucleophiles
    Chem. Ber. 1994, 127, 685 - 689.

  • 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.

  • K. Paulini, H.-U. Reißig*
    N-Silylation: New Possibilities for Long-Known Amines
    in "Organosilicon Chemistry: From Molecules to Materials" (N. Auner, J. Weis, Eds.), S. 65 - 66, VCH Verlagsgesellschaft 1994.

  • W. Adam, M. Ahrweiler, K. Paulini, H.-U. Reißig, V. Voerckel*
    Dimethyldioxirane Oxidation of Enamines: First Spectral Evidence for Enamine Oxides by Stabilization through N-Silylation
    Chem. Ber. 1992, 125, 2719 - 2722.

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

  • K. Paulini, H.-U. Reißig*
    Ein effektiver Weg zu GABA-analogen Aminosäuren: Cyclopropanierung von N-silylierten Allylaminen und Enaminen
    Liebigs Ann. Chem. 1991, 455 - 461.
Direct link

Publications

  • A Hölemann, H.-U. Reißig*
    Synthesis of New Furan Derivatives and 4-Hydroxy Aldehydes from 4-Hydroxy 1-Enol Ethers
    Synthesis 2004, 1963 – 1970.

  • A. Schmitt, H.-U. Reißig*
    Synthesis of 2-(Phenylselanyl)tetrahydrofurans from γ-Lactones and of γ-Hydroxydiselenoacetals from γ-Lactols
    Synthesis 2001, 867 - 870.

  • A. Schmitt, H.-U. Reißig*
    Lewis Acid Promoted Reactions of γ-Lactols with Silyl Enol Ethers - Stereoselective Formation of Functionalized Tetrahydrofuran Derivatives
    Eur. J. Org. Chem. 2001, 1169 - 1174.

  • A. Schmitt, H.-U. Reißig*
    On the Stereoselectivity of γ-Lactol Substitutions with Allyl- and Propargylsilanes - Synthesis of Disubstituted Tetrahydrofuran Derivatives
    Eur. J. Org. Chem. 2000, 3893 - 3901.

  • A. Schmitt, H.-U. Reißig*
    Stereoselective Substitution at Phenyl-Substituted γ-Lactols with Organometallic Compounds
    Chem. Ber. 1995, 128, 871 - 876.

  • A. Schmitt, H.-U. Reißig*
    A Highly Diastereoselective Route to Disubstituted Tetrahydrofuran Derivatives by Substitution of γ-Lactols with Silylated Nucleophiles
    Synlett 1990, 40 - 42.

  • H.-U. Reißig*, H. Holzinger, G. Glomsda
    A Titanoxycyclopropane as Intermediate in a Highly Stereoselective Homoaldol Type Addition - Syntheses of cis-Substituted Tetrahydrofuran Derivatives
    Tetrahedron-Symposium-in-Print on Strain-Assisted Synthesis (L. Ghosez, Ed.),
    Tetrahedron 1989, 45, 3139 - 3150.

  • C. Brückner, H. Holzinger, H.-U. Reißig*
    Diastereoselective Syntheses of Highly Substituted Methyl Tetrahydrofuran-3-carboxylates by Reactions of γ-Lactols with Silylated Nucleophiles
    J. Org. Chem. 1988, 53, 2450 - 2456.

  • C. Brückner, H. Lorey, H.-U. Reißig*
    Diastereoselektive Synthese funktionalisierter Tetrahydrofuran-Derivate aus γ-Lactolen
    Angew. Chem. 1986, 98, 559 - 560; Angew. Chem. Int. Ed. Engl. 1986, 25, 556 - 557.
Direct link

Publications

  • P. K. Patra, H.-U. Reißig*
    Functionalized Azamacrocycles and Large-Ring α-Amino Esters by One-Pot Syntheses from Methyl 2-Siloxy-2-vinylcyclopropanecarboxylates
    Eur. J. Org. Chem. 2001, 4195 – 4206.

  • P. K. Patra, H.-U. Reißig*
    An Efficient One-pot Synthesis of Functionalized Azamacrocycles from Methyl 2-Siloxy-2-vinylcyclopropane Carboxylates
    Synlett 2001, 33 - 36.

  • A. Ullmann, G. Zahn*, J. Schnaubelt, H.-U. Reißig
    Crystal Structure of Trimethyl 3-methyl-4-oxo-(E)-8-cyclodecene-1,1,6-
    tricarboxylate, C17H24O7

    Z. Kristallogr. NCS 1999, 214, 221 - 223.

  • A. Ullmann, M. Gruner, H.-U. Reißig*
    Synthesis of Functionalized Cyclophanes by Ring-Opening/Ring-Closure Cascade Reactions of Siloxycyclopropanes
    Chem. Eur. J. 1999, 5, 187 - 197.

  • A. Ullmann, H.-U. Reißig*, O. Rademacher
    A Repetitive Approach to the Synthesis of Medium and Large Ring Compounds with a Ring-Opening/Ring-Closure Cascade Reaction of Siloxycyclopropane Derivatives as Crucial Step
    Eur. J. Org. Chem. 1998, 2541 - 2549.

  • A. Ullmann, J. Schnaubelt, H.-U. Reißig* (Feature Article)
    Synthesis of Highly Functionalized Cyclodecenone Derivatives from Siloxycyclopropanes: Scope and Limitations
    Synthesis 1998, 1052 - 1066.

  • J. Schnaubelt, A. Ullmann, H.-U. Reißig*
    An Efficient One-Pot Synthesis of Functionalized Cyclodecenone Derivatives from Siloxycyclopropanes
    Synlett 1995, 1223 - 1225.
Direct link

Publications

  • H.-U. Reißig, R. Zimmer
    Nitrosoalkenes
    in Science of Synthesis (Knowledge Update) 2015/2, Thieme Verlag, Stuttgart, 315 – 334.

  • N. Moinizadeh, R. Klemme, M. Kansy, R. Zimmer,* H.-U. Reißig*
    Convenient Syntheses of Enantiopure 1,2-Oxazin-4-yl Nonaflates and Phosphates and Their Palladium-Catalyzed Cross-Couplings
    Synthesis 2013, 45, 2752 – 2762.

  • 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.

  • R. Zimmer, M. Buchholz, M. Collas, J. Angermann, K. Homann, H.-U. Reißig*
    1,2-Oxazines as Building Blocks for Stereoselective Synthesis: Preparation of Oxygen-Substituted 1,2-Oxazines, either by Alcohol Addition or by Epoxidation, and Subsequent Hydrogenation Leading to 1,2-Amino Alcohols and Pyrrolidines
    Eur. J. Org. Chem. 2010, 4111 – 4122.

  • 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.

  • R. Zimmer, M. Collas, R. Czerwonka, U. Hain, H.-U. Reißig*
    A New Access to Pyrrolizidine Derivatives: Ring Contraction of Methyl (E)-[1,2-Oxazin-3-yl]propenoates
    Synthesis 2008, 237 – 244.

  • H.-U. Reißig*, K. Homann, F. Hiller, R. Zimmer
    A Stereoselective Access to Dihydroxylated Pyrrolidines by Reductive Ring Contraction of 1,2-Oxazines.
    Synthesis, 2007, 2681 – 2689.

  • H.-U. Reißig, R. Zimmer*
    1-Nitrosoalkenes
    in: Science of Synthesis, 2006, Vol. 33, 371 – 389.

  • E. Schmidt, H.-U. Reißig*, R. Zimmer
    Regio- and Stereoselective 1,3-Dipolar Cycloadditions to 6H-1,2-Oxazines Leading to New Heterobicyclic Compounds
    Synthesis 2006, 2074 - 2084.

  • M. Buchholz, H.-U. Reißig*
    Enantioselective Syntheses of the Pyrrolidine Core of Endothelin Antagonist ABT-627 (Atrasentan) via 1,2-Oxazines
    Eur. J. Org. Chem. 2003, 3524 - 3533.

  • R. Zimmer, B. Orschel, S. Scherer, H.-U. Reißig*
    Hetero Diels-Alder Reactions of Nitroso Alkenes with Alkoxyallene Derivatives Bearing Carbohydrate Auxiliaries - Asymmetric Synthesis of 6H-1,2-Oxazines and Subsequent Reductive Transformations
    Synthesis 2002, 1553 - 1563.

  • M. Buchholz, F. Hiller, H.-U. Reißig*
    Synthesis of Enantioenriched 2-Substituted 4-Phenylbutylamines by Hydrogenolysis of Optically Pure 6-Alkoxy-5,6-dihydro-4H-1,2-oxazines
    Eur. J. Org. Chem. 2002, 2838 - 2843.

  • M. Buchholz, H.-U. Reißig*
    Highly Stereoselective and Flexible Synthesis of 6-Alkoxy-5,6-dihydro-4H-1,2-oxazines by Conjugate Addition of Organolithium Compounds to 6H-1,2-Oxazines Followed by Trapping with Electrophiles
    Synthesis 2002, 1412 - 1422.

  • A. A. Tishkov, H.-U. Reißig*, S. Ioffe
    Preparation of Cyclic and Bicyclic γ-Amino Acid Derivatives from Methyl 6-Ethoxy-5,6-dihydro-4H-1,2-oxazine-4-carboxylate
    Synlett 2002, 863 - 866.

  • H. Hartl*, I Brüdgam, H.-U. Reißig, M. Buchholz
    Crystal Structure of (4S*,5R*,6S*)-6-Ethoxy-4-(1R*)-(1-hydroxy-1-
    phenyl)methyl-3,5-diphenyl-5,6-dihydro-4H-1,2-oxazine, C25H25NO3
    Z. Kristallogr. NCS 2001, 216, 591 – 592.

  • E. Schmidt, H.-U. Reißig, O. Rademacher*
    Crystal structure of 3aS*,4S*,7aR*-4-ethoxy-3a,7a-dihydro-3,7-diphenyl-4H-1,5-
    dioxa-2,6-diaza-indene, C19H18N2O3

    Z. Kristallogr. NCS 2000, 215, 283 - 284.

  • R. Zimmer, K. Homann, J. Angermann, H.-U. Reißig*
    Stereoselective Preparation of 4,5-Dihydroxy-5,6-dihydro-4H-1,2-oxazines and Their Derivatives
    Synthesis 1999, 1223 - 1235.

  • D. Sperling, H.-U. Reißig, J. Fabian*
    1,3-Sigmatropic Rearrangements of Divinylcyclopropane Derivatives and Hetero Analogs in Competition with Cope-Type Rearrangements – A DFT Study
    Eur. J. Org. Chem. 1999, 1107 – 1114.

  • R. Zimmer, F. Hiller, H.-U. Reißig*
    1,4-Addition of Organolithium Compounds to 6-Ethoxy-3-phenyl-6H-1,2-oxazine
    Heterocycles 1999, 50, 393 - 401.

  • K. Homann, J. Angermann, M. Collas, R. Zimmer, H.-U. Reißig*
    Synthesis of 6-Ethoxy-6H-1,2-oxazines by Hetero Diels-Alder Reaction of 1-Bromo-2-ethoxyethene with α-Nitroso Alkenes
    J. Prakt. Chem. 1998, 340, 649 – 655.

  • U. Jänicke-Rößler, G. Zahn*, F. Hiller, H.-U. Reißig
    Crystal structure of (6S)-6-[(1R,2S,5R)-(–)-2-Ιsopropyl-5-methylcyclo-
    hexyloxy]-3-phenyl-6H-1,2-oxazine, [ONC(CH)3(C6H5)O(CH)2(CH2)2CHCH2CH(CH3)2CH3]

    Z. Kristallogr. 1998, 213, 261 - 262.

  • R. Zimmer, J. Angermann, U. Hain, F. Hiller, H.-U. Reißig*
    Hetero Diels-Alder Reactions of 2-Chloro-1-nitroso-1-phenylethene: Preparation of Novel 4-Chloro-Substituted 1,2-Oxazines and Subsequent Reactions
    Synthesis 1997, 1467 - 1474.

  • D. Sperling, A. Mehlhorn, H.-U. Reißig, J. Fabian*
    Theoretical Study of Pericyclic Reactions of Nitrosoethylene and (Thionitroso)ethylene
    Liebigs Ann. 1996, 1615 - 1621.

  • R. Zimmer, H.-U. Reißig*
    Lithiated 3-trifluoromethyl-substituted 1,2-Oxazines and their Reactions
    J. Fluorine Chem. 1996, 80, 21 - 26.

  • R. Zimmer, H.-U. Reißig*, K. Homann
    1,2-Azapyrylium Ions: Properties and Synthetic Applications
    J. Prakt. Chem. 1995, 337, 521 - 528.

  • J. Angermann, K. Homann, H.-U. Reißig*, R. Zimmer
    Synthesis and cis-Dihydroxylation of 6H-1,2-Oxazines - Synthesis of Dihydroxyprolinols
    Synlett 1995, 1014 - 1016.

  • K. Paulini, H.-U. Reißig*, P. Rademacher
    On the Reactivity of N,N-Bis(trimethyl)silylated Enamines: Model Studies on Hetero Diels-Alder Reactions and Other Cycloadditions
    J. Prakt. Chem. 1995, 337, 209 - 215.

  • K. Homann, R. Zimmer, H.-U. Reißig*
    Reactions of Azapyrylium Ions with Nucleophiles: From Crazy Products to a Novel Pyridine Synthesis
    Heterocycles 1995, 40, 531 - 537.

  • K. Paulini, A. Gerold, H.-U. Reißig*
    Reactions of 6-[Bis(trimethylsilyl)amino]-5,6-dihydro-4H-1,2-oxazines
    Liebigs Ann. 1995, 667 - 671.

  • T. Arnold, H.-U. Reißig, J. Richter, H. J. Lindner*, H. Paulus
    Crystal structure of 3-O-(5,6-dihydro-5-methyl-3-phenyl-4H-1,2-oxazin-6-yl)
    -1,2:5,6-di-O-isopropyliden-α-D-glucofuranose,
    O(CH)4OCO(CH3)2CHCH2OCO(CH3)2OCHCHCH2CNO(CH3)(C6H5)

    Z. Kristallogr. 1994, 209, 903 - 904.

  • K. Homann, H.-U. Reißig, S. Foro, H. J. Lindner*
    Crystal structure of 2-methyl-6-phenyl-pyridin-3-al, (C6H5)C(CH)2CCNCHO(CH3)
    Z. Kristallogr. 1994, 209, 902.

  • R. Zimmer, T. Arnold, K. Homann, H.-U. Reißig*
    An Efficient and Simple Synthesis of 3,4,5,6-Tetrahydro-2H-1,2-oxazines by Sodium Cyanoborohydride Reduction of 5,6-Dihydro-4H-1,2-oxazines
    Synthesis 1994, 1050 - 1056.

  • K. Paulini, H.-U. Reißig*
    Diastereoselective Radical Bromination of 5,6-Dihydro-4H-1,2-oxazines and Subsequent Substitution Reactions with Nitrogen Nucleophiles
    Chem. Ber. 1994, 127, 685 - 689.

  • R. Zimmer*, K. Homann, H.-U. Reißig*
    Reductive Transformations of 6H-1,2-Oxazines with Hydride Reagents: Formation of Aziridines and 3-Hydroxyalkylated 1,2-Oxazines
    Liebigs Ann. Chem. 1993, 1155 - 1157.

  • R. Zimmer, M. Hoffmann, H.-U. Reißig*
    Model Studies of the Reduction of 3-Phenyl-6H-1,2-oxazines, Chemo- and Stereoselectivity: Synthesis of Amino Alcohols, Amino Acids, and Related Compounds
    Chem. Ber. 1992, 125, 2243 - 2248.

  • T. Arnold, B. Orschel, H.-U. Reißig*
    Diacetonglucose als Hilfsgruppe bei der asymmetrischen Hetero-Diels-Alder-Reaktion mit Nitrosoalkenen
    Angew. Chem. 1992, 104, 1084 - 1086.

  • T. Arnold, B. Orschel, H.-U. Reißig*
    Diacetoneglucose as Auxiliary Group for the Asymmetric Hetero-Diels-Alder Reaction with Nitrosoalkenes
    Angew. Chem. Int. Ed. Engl. 1992, 31, 1033 - 1035.

  • R. Zimmer*, M. Collas, M. Roth, H.-U. Reißig
    6-Siloxy-Substituted 5,6-Dihydro-4H-1,2-oxazines as Key Building Blocks for Natural Products
    Liebigs Ann. Chem. 1992, 709 - 714.

  • R. Zimmer, H.-U. Reißig*, H.J. Lindner
    Unerwartete Bildung von β-Lactamen aus 6H-1,2-Oxazinen unter Lewis-Säure-Einwirkung
    Liebigs Ann. Chem. 1992, 621 - 624.

  • R. Zimmer, H.-U. Reißig*
    Efficient Synthesis of Trifluoromethyl-Substituted 5,6-Dihydro-4H-1,2-oxazines by the Hetero-Diels-Alder Reaction of 1,1,1-Trifluoro-2-nitroso-2-propene and Electron-Rich Olefins
    J. Org. Chem. 1992, 57, 339 - 347.

  • C. Unger, R. Zimmer, H.-U. Reißig*, E.-U. Würthwein
    Deprotonation of 5,6-Dihydro-5-methylene-4H-1,2-oxazines and Regioselective Reactions with Electrophiles
    Chem. Ber. 1991, 124, 2279 - 2287.

  • R. Zimmer, H.-U. Reißig*
    Synthesis of 6H-1,2-Oxazines by Hetero Diels-Alder Reactions of Nitroso Alkenes towards Methoxyallenes
    Liebigs Ann. Chem. 1991, 553 - 562.

  • H.-U. Reißig*, C. Hippeli
    Lithiated 5,6-Dihydro-4H-1,2-oxazines: Synthesis, Highly Diastereoselective Reactions with Electrophiles, and Subsequent Transformations
    Chem. Ber. 1991, 124, 115 - 127.

  • H.-U. Reißig*, C. Hippeli, T. Arnold
    On the Mechanism of Diels-Alder Reactions of Nitroso Alkenes: Exo/Endo-Selectivity, Stereospecificity, E/Z-Selectivity, and Relative Reactivity of Various Olefins
    Chem. Ber. 1990, 123, 2403 - 2411.

  • T. Arnold, H.-U. Reißig*
    Hetero Diels-Alder Reactions of Optically Active Enol Ethers with a Nitroso Alkene: Asymmetric Synthesis of 1,2-Oxazine Derivatives
    Synlett 1990, 514 - 516.

  • C. Hippeli, H.-U. Reißig*
    Reductive Transformations of 5,6-Dihydro-4H-1,2-oxazines: Synthesis of 4-Hydroxy Ketoximes, N-Hydroxypyrrolidine Derivatives, and Other Nitrogen Containing Compounds
    Liebigs Ann. Chem. 1990, 475 - 481.

  • C. Hippeli, R. Zimmer, H.-U. Reißig*
    Transition Metal and Acid-Induced Transformations of 6-Siloxy-Substituted
    5,6-Dihydro-4H-1,2-oxazines: Preparation of Pyrroles, Nitrones, 1,4-Dicarbonyl Compounds and Derivatives Thereof

    Liebigs Ann. Chem. 1990, 469 - 474.

  • C. Hippeli, H.-U. Reißig*
    Synthesis of Trialkylsiloxy-Substituted and Other 5,6-Dihydro-4H-1,2-oxazines by Hetero Diels-Alder Reactions of Nitroso Alkenes - Preparative Scope and Diastereoselectivity
    Liebigs Ann. Chem. 1990, 217 - 226.

  • C. Hippeli, N. Basso, F. Dammast, H.-U. Reißig*
    A Practical Method for the Separation of E/Z-Isomeric Silyl Enol Ethers by Kinetic Resolution
    Synthesis 1990, 26 – 27.

  • R. Zimmer, H.-U. Reißig*
    Nucleophile Substitution an 6H-1,2-Oxazinen über Azapyrylium-Ionen
    Synthesis 1989, 908 - 911.

  • R. Zimmer, H.-U. Reißig*
    Methoxyallene als Komponenten in Diels-Alder-Reaktionen mit inversem Elektronenbedarf: Synthese von 6H-1,2-Oxazinen
    Angew. Chem. 1988, 100, 1576 - 1577.

  • R. Zimmer, H.-U. Reißig*
    Methoxyallenes as Components in Diels-Alder Reactions with Inverse Electron Demand: Synthesis of 6H-1,2-Oxazines
    Angew. Chem. Int. Ed. Engl. 1988, 27, 1518 - 1519.

  • C. Hippeli, H.-U. Reißig*
    Highly Diastereoselective Deprotonation and Substitution of Chiral 5,6-Dihydro-4H-1,2-oxazines
    J. Org. Chem. 1988, 53, 3884 - 3886.

  • C. Hippeli, H.-U. Reißig*
    Efficient Synthesis of 6-Trimethylsiloxy- and 6-(Trimethylsilyl)methyl-3-phenyl-
    5,6-dihydro-4H-1,2-oxazines by Cycloaddition of α-Nitrosostyrene to Silyl Enol Ethers and Allyltrimethylsilane

    Synthesis 1987, 77 - 79.
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Publications

    • 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.

    • R. Zimmer,* V. Dekaris, M. Knauer, L. Schefzig, H.-U. Reißig
      Synthesis of Poly(Ethylene Glycol)-Supported (R)-BINOL Derivatives and Their First Application in Enantioselective Mukaiyama Aldol Reactions
      Synth. Commun. 2009, 1012 – 1026.

    • R. Zimmer*, L. Schefzig, A. Peritz, V. Dekaris, H.-U. Reißig
      Functionalized BINOL Derivatives as Ligands for Enantioselectively Catalyzed Aldol Additions: Highly Enantioselective Synthesis of Chiral β-Hydroxy Thioesters
      Synthesis 2004, 1439 – 1445.

    • R. Zimmer*, A. Peritz, R. Czerwonka, L. Schefzig, H.-U. Reißig
      Optimisation, Scope and Limitations of Enantioselective Aldol Reactions of an S-Ketene Silyl Acetal with Aliphatic Aldehydes under (R)-BINOL-Titanium(IV) Catalysis Conditions
      Eur. J. Org. Chem. 2002, 3419 – 3428.

    • M. Hölzer, W. Burd, H.-U. Reißig, K.-H. van Pée*
      Substrate Specificity and Regioselectivity of Tryptophan 7-Halogenase from Pseudomonas fluoreszens BL915
      Adv. Synth. Catal. 2001, 343, 591 – 595.

    • R. Zimmer*, U. Hain, M. Berndt, R. Gewald, H.-U. Reißig
      Enantioselective Synthesis of (S)- and (R)-6-Hydroxy-8-nonenecarboxylates by Asymmetric Catalysis: A Formal Synthesis of (R)-α-Lipoic Acid and its (S)-Antipode
      Tetrahedron: Asymmetry 2000, 11, 879 - 887.

    • H. Scheytza, H.-U. Reißig, O. Rademacher*, F. Hahn, J. Richter
      Crystal Structure of 5,13,20,27-Tetraazonia-32-thiaheptacycloy
      [25.2.2.22,5.213,16.217,20.17,11.122,25]-nonatriaconta-
      2,4,7,9,11(37),13,15,17,19,22,24,27,29,30,33,35,38-heptadecaene Tetrakis(hexafluorophosphate),
      C34H30F24N4P4S

      Z. Kristallogr. NCS 2000, 215, 75 - 76.

    • H. Scheytza*, O. Rademacher, H.-U. Reißig
      Synthesis and Structures of Novel Pyridine-Bridged Phanes of 4,4'-Bipyridine
      Eur. J. Org. Chem. 1999, 2373 - 2381.

    • H. Scheytza*, H.-U. Reißig, O. Rademacher
      Novel Furan-, Thiophene- and Benzo[b]thiophene Bridged Macrocycles of 4,4'-Bipyridine
      Tetrahedron 1999, 55, 4709 - 4720.

    • H. Scheytza*, H.-U. Reißig
      Unexpected Decomposition of a Monoquarternated 4,4'-Bipyridinium Dication by Disodium Dithionite Reduction in Water
      Tetrahedron 1999, 55, 1057 - 1062.

    • R. Zimmer, H.-U. Reißig*
      Reaction of Cyclooctyne with Fischer Carbene Complexes - Synthesis of Tricyclic Quinone Derivatives
      J. Prakt. Chem. 1998, 340, 755 - 756.

    • H. Scheytza*, H.-U. Reißig
      Cyclo(paraquat-o-phenylene-paraquat-p-phenylene) - The Missing Isomeric Carbophane of 4,4'-Bipyridine
      Tetrahedron Lett. 1998, 39, 8637 - 8640.

    • W. Adam*, D. Reinhardt, H.-U. Reißig, K. Paulini
      Epoxidation of Vinylamides by Dimethyldioxirane: First Spectral Evidence for Enamide Oxides
      Tetrahedron 1995, 51, 12257 - 12262.

    • T. Hafner, H.-U. Reißig*
      (S)-5-Nitro-2-pentanol durch Reduktion mit Bäckerhefe
      Liebigs Ann. Chem. 1989, 937 – 938.

    • R. Zschiesche, H.-U. Reißig*
      An Efficient Synthesis of 5-Membered Cyclic Nitrones from γ-Nitro Ketones
      Tetrahedron Lett. 1988, 29, 1685 – 1686.

    • E. Piers*, M.S. Burmeister, H.-U. Reißig
      Thermal Rearrangement of Functionalized 1,2-Divinylcyclopropane Systems. A Convenient Synthesis of Substituted 4-Cyclohepten-1-ones
      Can. J. Chem. 1986, 64, 180 – 187.

    • H. Bader, H.-U. Reißig*
      The First 4-Dialkylamino-1,2-dihydropyridine Derivatives: Synthesis and Basic Reactions
      Tetrahedron 1986, 42, 835 – 838.

    • M. Horner, S. Hünig*, H.-U. Reißig
      Reversible Umwandlung eines [4]-Radialens in ein Cyclobutadien durch vierstufige Elektronenübertragung
      Liebigs Ann. Chem. 1983, 658 – 667.

    • E. Hirsch, S. Hünig*, H.-U. Reißig
      Darstellung von (2,2-Dimethyl-1-methylenpropyl)methansulfonat und -trifluoracetat
      Chem. Ber. 1982, 115, 399 – 401.

    • R. Knorr*, E. Lattke, F. Ruf, H.-U. Reißig
      Vinyl-to-Benzyl Isomerization and Electrocyclizations in Lithio Derivatives of o-Tolylstilbenes
      Chem. Ber. 1981, 114, 1592 – 1599.

    • H.-U. Reißig*, B. Scherer
      A Simple Synthesis of Thiol Esters from Copper-I-Mercaptides and Acyl Chlorides
      Tetrahedron Lett. 1980, 21, 4259 – 4262.

    • E. Piers*, H.-U. Reißig
      Synthese von cis-2-Vinylcyclopropylketonen: neue Synthese von 4-Cycloheptenonen
      Angew. Chem. 1979, 91, 857 – 858.

    • E. Piers*, H.-U. Reißig


Synthesis of cis-2-Vinylcyclopropyl Ketones: a New Synthesis of 4-Cycloheptenones
Angew. Chem. Int. Ed. Engl.1979

      ,

18

      , 791 – 792.
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