The application of a convenient one-pot synthetic strategy, utilizing an in situ formed organocatalyst, to the enantioselective synthesis of anti-leukaemia agent (R)-convolutamydine A has been demonstrated.
Department of Chemistry and Pharmacy, Organic Chemistry Chair I and Interdisciplinary Center for Molecular Materials, University of Erlangen-Nürnberg, Henkestraße 42, 91054, Erlangen, Germany
Department of Chemistry and Pharmacy, Organic Chemistry Chair I and Interdisciplinary Center for Molecular Materials, University of Erlangen-Nürnberg, Henkestraße 42, 91054, Erlangen, Germany
Department of Chemistry and Pharmacy, Organic Chemistry Chair I and Interdisciplinary Center for Molecular Materials, University of Erlangen-Nürnberg, Henkestraße 42, 91054, Erlangen, Germany
Department of Chemistry and Pharmacy, Organic Chemistry Chair I and Interdisciplinary Center for Molecular Materials, University of Erlangen-Nürnberg, Henkestraße 42, 91054, Erlangen, Germany
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