Photoredox-Catalyzed Regio- & Stereoselective C(sp²)–H Cyanoalkylation of Enamides with Cycloketone OximesviaSelective C-C Bond Cleavage/Radical Addition Cascade

Ting Guan,†^a,dJing-Yu Guo,†^a,dQing-Hong Zhang,^aXin-Wen Xu,^aXiao-Yu Yu,^aYu Zhang,^band Kai Zhao*^a,c

^aInstitute of Advanced Synthesis, School of Chemistry and Molecular Engineering, Jiangsu National Synergetic Innovation Center for Advanced Materials, Nanjing Tech University, Nanjing 211816, China

^bCollege of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, China

^cGuangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology, Shenzhen 518055, China

^dPharmaBlock Sciences (Nanjing), Inc, 10 Xuefu Road, Jiangbei New Area, Nanjing, 210032, China

Abstract:A photoredox-catalyzed regio- and stereoselective Heck-type cyanoalkylation of synthetically prominent enamides with cycloketone oximes via selectiveβ-C-C bond scission/selective radical addition cascade is developed, enabling the incorporation of synthetically versatile and pharmaceutically appealing distal cyanoalkyl moieties into enamide scaffolds under mild conditions. The synthetic importance of this methodology was highlighted by the broad substrate scopes, satisfying functional group compatibilities, excellent regio- and stereoselectivities as well as the versatile and diverse synthetic applications ofβ-cyanoalkylated enamides.

Green Chemistry.2022,24,6524–6530. (2021年影响因子:11.034).

论文链接：https://doi.org/10.1039/D2GC01978G