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Oxidative Functionalization of Silyl Enol Ethers

Reactions of silyl enol ethers with iodosylbenzene in the presence of BF3-Et20 can be used to form new carbon-carbon bonds [209], prepare a-substituted ketones [210] and synthesize oxygen-containing [Pg.171]

A similar intramolecular oxidation of silyl enol ether 158 affords oxygen heterocycle 159 [Pg.172]

Hypervalent Iodine Reagents in Organic Synthesis 173 Bp3 Et20, (EtO)3P, CH2CI2, 0 to 25 C P O [Pg.173]

See other pages where Oxidative Functionalization of Silyl Enol Ethers is mentioned: [Pg.171]   


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Enol ethers oxidation

Enolate, oxidation

Enolates oxidation

Enolates silylation

Enols oxidation

Ethers oxidation

Functionalizations oxidative

Of silyl enol ethers

Oxidation functionalization

Oxidation of Enols

Oxidation of enol ether

Oxidation of enolate

Oxidation of ethers

Oxidation of silyl enol ethers

Oxidation silyl enolates

Oxide function

Oxidizing function

Silyl enol ethers

Silyl enol ethers oxidation

Silyl enol ethers, oxidative functionalization

Silyl enolate

Silyl enolates

Silyl functions

Silylation of Enolates

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