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E Miscellaneous Reactions

Miscellaneous Reactions.—Desulphurization of S-labelled benzyl trisulphide (119) with triphenylphosphine leads to predominant removal of the central sulphur atom, while reaction with tris(diethylamino)- [Pg.90]

A useful new method of preparing arylphosphonates (123) involves the reaction of trialkyl phosphites with aryl halides in the presence of a nickel catalyst.The suggested mechanism is via the nickel complex (124), and is non-radical. [Pg.90]

Japanese workers have prepared diethyl phosphite in 43% yield from the reaction of white phosphorus with ethanol and oxygen. [Pg.91]

See other pages where E Miscellaneous Reactions is mentioned: [Pg.583]    [Pg.653]    [Pg.583]    [Pg.653]    [Pg.8]    [Pg.122]    [Pg.364]    [Pg.185]    [Pg.239]    [Pg.2464]    [Pg.2504]    [Pg.257]    [Pg.283]    [Pg.73]    [Pg.89]    [Pg.41]    [Pg.74]    [Pg.428]    [Pg.83]    [Pg.313]    [Pg.328]    [Pg.101]    [Pg.433]    [Pg.434]    [Pg.436]    [Pg.546]    [Pg.575]    [Pg.585]    [Pg.649]    [Pg.205]    [Pg.185]    [Pg.239]    [Pg.428]    [Pg.300]    [Pg.365]    [Pg.894]    [Pg.940]    [Pg.790]    [Pg.790]    [Pg.844]    [Pg.869]    [Pg.47]    [Pg.314]    [Pg.2464]    [Pg.2504]   


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E reactions

Miscellaneous reactions

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