Abstract
A series of phosphine oxides and H-phosphinates were vinylated in the presence of the iodine(iii) reagents vinylbenziodoxolones (VBX), providing the corresponding alk-1-enyl phosphine oxides and alk-1-enyl phosphinates in good yields with complete chemo- and regioselectivity. The vinylation proceeds in open flask under mild and transition metal-free conditions.
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CITATION STYLE
APA
Castoldi, L., Rajkiewicz, A. A., & Olofsson, B. (2020). Transition metal-free and regioselective vinylation of phosphine oxides and: H -phosphinates with VBX reagents. Chemical Communications, 56(92), 14389–14392. https://doi.org/10.1039/d0cc05992g
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