對二取代的噁唑烷酮稠合吖環丙烷使用一、二和三級醇，進行酸催化開環反應的研究。此方法反應時間短，並且在室溫下就能進行反應，得到開環化合物，可提高合成效率。並且利用此開環方法合成 2-胺基醚化合物。;Acid-catalyzed ring-opening reactions of disubstituted oxazolidinone-fused aziridines with primary, secondary, and tertiary alcohols were investigated. This method enables efficient ring-opening under mild conditions and short reaction times at room temperature, affording the corresponding ring-opened products. Furthermore, this strategy was applied to the synthesis of 2-amino ether derivatives.
