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Organo Tellurium Cyanides

The reactions of organo tellurium cyanides are largely unexplored. Benzyl tellurium cyanides reacted with the stoichiometrically required amounts of bromine to yield benzyl tellurium tribromides4,5. An excess of bromine caused deposition of tellurium and the formation of benzyl bromide5. [Pg.369]

Organo tellurium halides treated with potassium or silver cyanide were converted to organyl tellurium cyanides (p. 366). [Pg.251]

From Organo Tellurium Halides and Metal Cyanides... [Pg.366]

Exchange of halide for cyanide in organo tellurium halides occurs easily when the tellurium halide is fused with anhydrous silver cyanide4 or treated with potassium cyanide in methanol5, DMSO6 or ethanol/dimethyl sulfoxide7. [Pg.366]

See other pages where Organo Tellurium Cyanides is mentioned: [Pg.236]    [Pg.366]    [Pg.367]    [Pg.369]    [Pg.707]    [Pg.236]    [Pg.236]    [Pg.366]    [Pg.367]    [Pg.369]    [Pg.707]    [Pg.236]    [Pg.366]    [Pg.367]    [Pg.369]    [Pg.707]    [Pg.236]    [Pg.236]    [Pg.366]    [Pg.367]    [Pg.369]    [Pg.707]    [Pg.850]    [Pg.236]    [Pg.838]    [Pg.625]    [Pg.62]    [Pg.850]    [Pg.625]    [Pg.391]    [Pg.390]   


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Cyanides organo

From Organo Tellurium Halides and Metal Cyanides

Tellurium Cyanide

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