Modular and Practical 1,2-Aryl(Alkenyl) Heteroatom Functionalization of Alkenes through Iron/Photoredox Dual Catalysis** |
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Authors: | Dr Weigang Zhang Tao Liu Dr Hwee Ting Ang Penghao Luo Zhexuan Lei Xiaohua Luo Prof Dr Ming Joo Koh Prof Dr Jie Wu |
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Institution: | Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore, 117543 Singapore |
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Abstract: | Efficient methods for synthesizing 1,2-aryl(alkenyl) heteroatomic cores, encompassing heteroatoms such as nitrogen, oxygen, sulfur, and halogens, are of significant importance in medicinal chemistry and pharmaceutical research. In this study, we present a mild, versatile and practical photoredox/iron dual catalytic system that enables access to highly privileged 1,2-aryl(alkenyl) heteroatomic pharmacophores with exceptional efficiency and site selectivity. Our approach exhibits an extensive scope, allowing for the direct utilization of a wide range of commodity or commercially available (hetero)arenes as well as activated and unactivated alkenes with diverse functional groups, drug scaffolds, and natural product motifs as substrates. By merging iron catalysis with the photoredox cycle, a vast array of alkene 1,2-aryl(alkenyl) functionalization products that incorporate a neighboring azido, amino, halo, thiocyano and nitrooxy group were secured. The scalability and ability to rapid synthesize numerous bioactive small molecules from readily available starting materials highlight the utility of this protocol. |
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Keywords: | Difunctionalization Iron Catalyst Late-Stage Functionalization Metallaphotoredox Multicomponent |
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