Liye Ma, Lvqi Jiang, Guangsheng Tian, Zijian Lin, Zhongquan Lin, Yu Xu, Zihao Guo, Leibing Wang, Jie Liu, Wen-Bin Yi
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引用次数: 0
Abstract
The distinctive chemical properties of fluorine atoms have enabled fluorine-containing compounds to make significant strides in the pharmaceutical and materials fields. However, due to the very limited synthetic methods, the enormous potential of N-monofluoromethyl compounds has not yet been unlocked. In this study, we present an operationally simple and practical protocol for various largely underexplored N-monofluoromethyl compounds, utilizing two powerful and isolable building blocks: N-CH2F thio carbamoyl fluorides and N-CH2F carbamoyl fluorides. Additionally, the reactivity of fluorine atoms located at different positions of the two building blocks toward nucleophilic substitution was investigated both experimentally and theoretically.