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Triphenylmethyl halide reduction

The reduction of arylalkyl halides of the triphenylmethyl type by electro-chemically generated outer sphere single electron donors offers an example of a sequencing of the bond-breaking and electron-transfer steps different from what has been described before. The cleavage of the halide ion then precedes electron transfer which thus involves the carbocation, a mechanism reminiscent of 8, 1 reactions (Andrieux et ai, 1984b) as shown in (102). The... [Pg.69]

See other pages where Triphenylmethyl halide reduction is mentioned: [Pg.70]    [Pg.12]    [Pg.440]    [Pg.441]    [Pg.1238]    [Pg.456]    [Pg.615]    [Pg.650]    [Pg.12]   
See also in sourсe #XX -- [ Pg.69 ]



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