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1. Chiral N-acyliminium ions as new tools in the asymmetric synthesis of CNS-active compounds


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2. Tetrahydro-3-pyranon: Regioselektivität bei der Bildung reaktiver Intermediate


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3. Synthesen und Ringverengungsreaktionen alpha-halogenierter N-Phenylcamphersäureimide


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4. Neue chirale Hilfsgruppen: Gewinnung einer phenylazaanalogen Camphansäure nach veränderter N/O-Regioselektivität einer Ringverengungsreaktion


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5. Tetrahydro-3-pyranon als Baustein zur Pyrano[3,2-b]pyran-Synthese


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6. Regiospezifische Synthese von 2-Phenyl-pyrano[3,4-b]pyranonen (Oxaflavon-Derivaten) mit Tetrahydro-3-pyranon


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7. Pyrano- und Naphthopyrano[3,2-b]indol-Derivate


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8. Cyclobutanon-Enamine: Synthese und Reaktionen des N-(1-Cyclobutenyl)-piperidins


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9. Asymmetrische elektrophile alpha-Amidoalkylierung, 4. Mitt.


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10. Asymmetrische elektrophile alpha-Amidoalkylierung, 3.Mitt.: Synthesen von Vorstufen für die Erzeugung chiraler N-Acylpyrrolidiniumionen


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