Baldon Simone, Paut Julien, Anselmi Elsa, Dagousset Guillaume, Tuccio Béatrice, Pelosi Giorgio, Cuadros Sara, Magnier Emmanuel, Dell'Amico Luca
Department of Chemical Sciences, University of Padova Via Francesco Marzolo 1 35131 Padova Italy
Institut Lavoisier de Versailles, Université Paris-Saclay 45 avenue des Etats-Unis 78035 Versailles France
Chem Sci. 2025 Mar 14;16(16):6957-6964. doi: 10.1039/d5sc01068c. eCollection 2025 Apr 16.
Herein, we report a metal-free divergent visible-light driven method for the synthesis of fluorinated sulfoximines. Both olefins and propellanes efficiently undergo difluorosulfoximination with yields up to 77% (65 examples). The process is general and robust and tolerates diverse functional groups, including esters, ethers, ketones, silyl groups, silyl ethers or boronic esters. The functionalization of diverse bioactive ingredients (8 examples) and various product manipulations demonstrate the synthetic usefulness of the developed synthetic platform. Finally, we rationalized the divergent reaction mechanism by performing Stern-Volmer quenching and EPR experiments that revealed the key activity of a difluoroalkyl sulfoximine radical.
在此,我们报道了一种无金属的发散型可见光驱动合成氟化亚砜亚胺的方法。烯烃和螺桨烷都能有效地进行二氟亚砜亚胺化反应,产率高达77%(65个实例)。该过程具有通用性和稳健性,能耐受多种官能团,包括酯基、醚基、酮基、硅基、硅醚或硼酸酯。多种生物活性成分的官能团化(8个实例)以及各种产物操作证明了所开发合成平台的合成实用性。最后,我们通过进行斯特恩-沃尔默猝灭和电子顺磁共振实验来阐明发散反应机理,这些实验揭示了二氟烷基亚砜亚胺自由基的关键活性。