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Tris silane with phenyl radical

In the simplest application of this concept, Chatgilialoglu and Curran carried out allylation reactions with allyl phenyl sulfones in the presence of tris(trimethylsilyl)-silane [58]. These reactions are analogous to the tin-mediated reactions previously discussed however, tris(trimethylsilyl)silane is used instead of tributyltin hydride or hexabutylditin for propagating the radical chain. The yields in these reactions ranged from moderate to good. [Pg.64]

Allyl[tris(trimethylsilyl)]silanes. These valuable synthetic reagents are prepared by free-radical substitution of allyl phenyl sulfides with (MejSiljSiH. They can be used as radical-based allylating agents. [Pg.168]


See other pages where Tris silane with phenyl radical is mentioned: [Pg.690]    [Pg.90]    [Pg.690]    [Pg.78]    [Pg.96]    [Pg.1572]    [Pg.91]    [Pg.99]    [Pg.117]    [Pg.167]    [Pg.2]    [Pg.1572]    [Pg.35]   
See also in sourсe #XX -- [ Pg.36 ]




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2.4.6- Tris phenyl

Phenyl radical

Radical phenylative

Radicals silanes

Silane phenyl

Silanes tris

With silane

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