Hamada Mayo, Orimoto Gaku, Yoshida Suguru
Department of Biological Science and Technology, Faculty of Advanced Engineering, Tokyo University of Science, 6-3-1 Niijuku, Katsushika-ku, Tokyo 125-8585, Japan.
Chem Commun (Camb). 2024 Jul 25;60(61):7930-7933. doi: 10.1039/d4cc02723j.
An efficient triple-click assembly using a newly designed trivalent platform is disclosed. We achieved the selective azaylide formation of 2,3,5,6-tetrafluorophenyl azides with -ester-substituted triarylphosphines leaving 2,6-dichlorophenyl azides untouched. Further rapid Staudinger reaction of dichlorophenyl azides and subsequent triazole formation allowed us to prepare trifunctionalized molecules in three steps.
公开了一种使用新设计的三价平台的高效三点击组装方法。我们实现了2,3,5,6-四氟苯基叠氮化物与酯取代的三芳基膦的选择性氮杂叶立德形成,而2,6-二氯苯基叠氮化物未受影响。二氯苯基叠氮化物的进一步快速施陶丁格反应及随后的三唑形成使我们能够通过三步制备三官能化分子。