Organisch-Chemisches Institut, Heidelberg University, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany.
Chemistry Department, Faculty of Science, King Abdulaziz University (KAU), Jeddah 21589, Saudi Arabia.
Org Lett. 2020 Aug 7;22(15):5844-5849. doi: 10.1021/acs.orglett.0c01924. Epub 2020 Jul 17.
Saturated heterocyclic acetals are useful fragments in organic synthesis and other fields. Herein, C(sp)-H dehydrogenative cross-couplings of ethers, tetrahydrothiophenes, and pyrrolidines were achieved under visible light irradiation by using iodobenzene and an in situ-formed gold complex. The broad functional group compatibility and substrate scope indicate that our strategy is a promising way to synthesize acetal analogues. The method was successfully applied in late-stage modifications of bioactive molecules. Gram scale syntheses and mechanistic studies are also presented.
饱和杂环缩醛在有机合成和其他领域是非常有用的片段。在此,通过使用碘苯和原位生成的金配合物,在可见光照射下实现了醚类、四氢噻吩和吡咯烷的 C(sp 3 )-H 脱氢交叉偶联。广泛的官能团兼容性和底物范围表明,我们的策略是合成缩醛类似物的一种很有前途的方法。该方法成功地应用于生物活性分子的后期修饰。还进行了克级合成和机理研究。