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Substitution Reactions at γ-Lactols

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.