Abstract
AbstractDas aus Clindamycin (I) und Anisaldehyd erhältliche Anisylidenderivat (II) ergibt durch Acylierung die geschützten 2‐Monoester (III), die beim Erhitzen mit Säuren unter Abspaltung der Schutzgruppe die freien 2‐Monoester (IV) liefern.
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