Search Results - Schambony, Simon B.

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  1. 1
    A Highly Diastereoselective Dioxetane Formation by the Hydroxy-Directed [2+2] Cycloaddition of Singlet Oxygen to a Chiral Allylic Alcohol

    A Highly Diastereoselective Dioxetane Formation by the Hydroxy-Directed [2+2] Cycloaddition of Singlet Oxygen to a Chiral Allylic Alcohol by Adam, Waldemar, Saha-Möller, Chantu R, Schambony, Simon B

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  2. 2
    Diastereoselective Epoxidation of Oxazolidine-Substituted Alkenes by Dimethyldioxirane and m-Chloroperbenzoic Acid:  π-Facial Control through Hydrogen Bonding by the Urea Functionality

    Diastereoselective Epoxidation of Oxazolidine-Substituted Alkenes by Dimethyldioxirane and m-Chloroperbenzoic Acid:  π-Facial Control through Hydrogen Bonding by the Urea Functiona... by Adam, Waldemar, Schambony, Simon B

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  3. 3
    Efficient Control of the Diastereoselectivity and Regioselectivity in the Singlet-Oxygen Ene Reaction of Chiral Oxazolidine-Substituted Alkenes by a Remote Urea NH Functionality:  Comparison with Dimethyldioxirane and m-Chloroperbenzoic Acid Epoxidations

    Efficient Control of the Diastereoselectivity and Regioselectivity in the Singlet-Oxygen Ene Reaction of Chiral Oxazolidine-Substituted Alkenes by a Remote Urea NH Functionality: ... by Adam, Waldemar, Peters, Karl, Peters, Eva-Maria, Schambony, Simon B

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  4. 4
    Stereocontrolled Photooxygenations-A Valuable Synthetic Tool

    Stereocontrolled Photooxygenations-A Valuable Synthetic Tool by Adam, Waldemar, Saha-Möller, Chantu R., Schambony, Simon B., Schmid, Katharina S., Wirth, Thomas

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  5. 5
    Diastereoselective and Regioselective Singlet-Oxygen Ene Reaction of Oxazolidine-Substituted Alkenes:  Control through Hydrogen Bonding Mediated by the Urea Functionality of Chiral Auxiliaries

    Diastereoselective and Regioselective Singlet-Oxygen Ene Reaction of Oxazolidine-Substituted Alkenes:  Control through Hydrogen Bonding Mediated by the Urea Functionality of Chiral... by Adam, Waldemar, Peters, Karl, Peters, Eva-Maria, Schambony, Simon B.

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