Department of Natural Medicine, School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai 201203, China.
Chem Commun (Camb). 2022 Sep 27;58(77):10841-10844. doi: 10.1039/d2cc03984b.
An efficient approach to access α-arylacetylene-substituted pyrrolidine and piperidine derivatives has been developed through a samarium diiodide-mediated addition-elimination process of pyrrolidine and piperidine -α-radicals with arylacetylene sulfones.
一种通过钐二碘化物介导的吡咯烷和哌啶-α-自由基与芳基乙炔亚砜的加成-消除过程来获得α-芳基乙炔取代的吡咯烷和哌啶衍生物的有效方法已经被开发出来。