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Diorgano Tellurium Imides

Diaryl tellurium oxides and carboxylic acid amides react in refluxing chloroform to produce diaryl tellurium imides Sulfonamides react similarly  [Pg.650]

Diaryl tellurium oxides in hot chloroform react with trichloroacetonitrile to give diaryl tellurium trichloroacetimides  [Pg.651]

Alkyl phenyl telluriums react with AT-chloro-A-sodio-4-methylbenzenesulfonamide in refluxing THF to yield terminal olefins from prim, alkyl groups and a mixture of 1 -alkenes and 2-alkenes from sec. alkyl groups. Diorgano tellurium imides were postulated as intermediates. Considering the synthesis of the alkyl phenyl tellurium from an alkyl halide and benzenetellurolate, the overall reaction is the conversion of an alkyl halide to an olefin. Starting with lithiomethyl phenyl tellurium and an alkyl halide, the resulting olefin will have one carbon atom more than the alkyl halide. ... [Pg.481]

See other pages where Diorgano Tellurium Imides is mentioned: [Pg.481]    [Pg.650]    [Pg.661]    [Pg.663]    [Pg.665]    [Pg.650]    [Pg.661]    [Pg.663]    [Pg.665]    [Pg.481]    [Pg.650]    [Pg.661]    [Pg.663]    [Pg.665]    [Pg.650]    [Pg.661]    [Pg.663]    [Pg.665]    [Pg.661]   


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Diorgano

Tellurium imide

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