Photocatalytic alkene reduction by a B12–TiO2 hybrid catalyst coupled with C–F bond cleavage for gem-difluoroolefin synthesis†
Abstract
Photocatalytic syntheses of gem-difluoroolefins were performed using the B12–TiO2 hybrid catalyst during the C![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) C bond reduction of α-trifluoromethyl styrenes with C–F bond cleavage at room temperature under nitrogen. The gem-difluoroolefins were used as synthetic precursors for fluorinated cyclopropanes.
C bond reduction of α-trifluoromethyl styrenes with C–F bond cleavage at room temperature under nitrogen. The gem-difluoroolefins were used as synthetic precursors for fluorinated cyclopropanes.
 
                




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