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Without Cleavage of a Te —C Bond

Alkyl vinyl telluriums were converted to the dichlorides by sulfuryl chloride in petroleum ether. In this cases the carbon-carbon double bond remained unaffected . [Pg.469]

The halogens required for this reaction may be generated in situ, for example, through oxidation of hydrogen halides by copper(II) acetate . Organic vicinal dibromides release their bromine atoms to tellurium  [Pg.469]

Interhalogen compounds produce diorgano tellurium dihalides with two different halogen/pseudohalogen atoms bonded to tellurium . [Pg.469]

de Moura Campos, N. Petragnani, C. Thome, Tetrahedron Lett. 1960, 5. [Pg.469]

Thiocyanogen oxidizes diorgano telluriums to diorgano tellurium dithiocyanates.  [Pg.470]

See other pages where Without Cleavage of a Te —C Bond is mentioned: [Pg.469]    [Pg.569]    [Pg.704]    [Pg.712]    [Pg.469]    [Pg.569]    [Pg.704]    [Pg.712]    [Pg.469]    [Pg.569]    [Pg.704]    [Pg.712]    [Pg.469]    [Pg.569]    [Pg.704]    [Pg.712]    [Pg.446]    [Pg.4271]    [Pg.262]   


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C cleavage

C-0 bond cleavage

Cleavage of C— bond

Cleavage of bonds

TESS

Without Cleavage of Te —C Bonds

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