A diastereoselective three-component cascade reaction, catalyzed by p-sulfonic acid calix[4]arene, provides a unique method to access diverse julolidine derivatives in high yields. Additionally, the reaction was also monitored by mass spectrometry and the mechanistic pathway uncovered.
在p-
磺酸杯[4]
芳烃的催化下,一种非对映选择性三组分级联反应为高产量地获得多种朱洛利定衍
生物提供了一种独特的方法。此外,该反应还通过质谱法进行了监测,并揭示了反应机理。