We presented a cascade transformation of N, N-diallylamines and fluoroalkyl iodides into various functionalized fluoroalkylated pyrrolidines through a visible light-induced synthetic process in the solvent-free conditions. In this reaction system, the substrate N, N-diallylamine acted both as the base and the electron donor. We further demonstrated the practicality of this protocol by the direct modification
我们提出了在无溶剂条件下通过可见光诱导合成过程将N , N-
二烯丙基胺和氟烷基
碘化物级联转化为各种功能化氟烷基化
吡咯烷。在该反应体系中,底物N,N-二
烯丙胺既充当碱基又充当电子供体。我们通过
氨基酸和药物分子的直接修饰进一步证明了该方案的实用性。