Photochemical oxyfluoroalkylation of styrenes by the addition of perfluoroalkyl radicals in an atmosphere of oxygen
β Scribed by Masato Yoshida; Masanori Ohkoshi; Nobuyuki Aoki; Yuki Ohnuma; Masahiko Iyoda
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 224 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The photochemical reaction of perfluoroalkyl iodide with o~-methylstyrene and related compounds in the presence of hexabutylditin under oxygen atmosphere produces the fluoroalkylated alcohols in good yields. The reaction was photochemicaily initiated, and proceeded via a radical chain mediated by the ditin.
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## Abstract Direct observation of the unstable intermediate in the radical addition reaction of the oxime ether 1 mediated by triethylborane (Et~3~B) is described using ^1^H and ^11^B micro channeled cell for synthesis monitoring (MICCS), which was recently developed as an interfacing microchip for
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