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Aryl halide reduction, single electron

Radicals can also be generated via the fragmentation of radical anions. Single electron reduction of various alkyl or aryl halides will lead to bond cleavage, as shown in Eqs. 10.44 and 10.45. The reductions commonly occur from dissolving metals such as Na and K, sodium naphthalenide (Na Ar ), sodium benzophenone ketyl, or from pulse radiolysis (e ). [Pg.570]

See other pages where Aryl halide reduction, single electron is mentioned: [Pg.167]    [Pg.149]    [Pg.425]    [Pg.270]    [Pg.270]    [Pg.424]    [Pg.1866]    [Pg.270]    [Pg.44]    [Pg.211]    [Pg.425]    [Pg.249]    [Pg.498]    [Pg.417]   


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Aryl halide, reduction

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Single-electron reductant

Single-electron reduction

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