The present invention provides a method for synthesizing 1-(acyloxy)-alkyl derivatives from 1-acyl-alkyl derivatives, which typically proceeds stereospecifically, in high yield, does not require the use of activated intermediates and/or toxic compounds and is readily amendable to scale-up. The current invention also provides 1-acyl-alkyl derivatives of known drug components and methods for synthesizing these 1-acyl-alkyl derivatives.
本发明提供了一种从1-酰基-烷基衍
生物合成1-(酰氧基)-烷基衍
生物的方法,该方法通常具有立体特异性,在高收率下进行,不需要使用活化中间体和/或有毒化合物,易于扩大规模。本发明还提供了已知药物成分的1-酰基-烷基衍
生物及其合成方法。