Abstract:Durch O‐Acylierung (in siedendem Benzol, 24‐75 h) der entsprechenden Alkohole mit dem betreffenden Säurechlorid (Cl‐BPA) werden die Ester (I)‐(VI) dargestellt [bei der Darstellung von (III) und (IV) findet als Neben‐ 141R reaktion N‐Acylierung statt (Ausb. in g angegeben)].
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