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Generation of a-Silyl Carbanions by Tin-Lithium Transmetallation

Formation of )9-Hydroxyalkylsilanes from Silyl Enol Ethers [Pg.60]

Silyl enol ethers have been known to undergo aldol condensations with aldehydes in the presence of Lewis acids [260, 261]. When a silyl group occupies the [Pg.60]

These methodologies are also effective for the synthesis of a,j8-unsaturated cyclic esters and amides [267, 268]. For example, a, 8-unsaturated y-lactone 149 is syn- [Pg.61]

R = alkyl, alkenyl, aryl, heteroaryl catalyst = ZnBr2, Hgl2, NaF, CsF [Pg.62]


See other pages where Generation of a-Silyl Carbanions by Tin-Lithium Transmetallation is mentioned: [Pg.60]   


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A-silyl

A-silyl carbanion

By Lithium

Carbanions generation

Carbanions lithium

Generation of Carbanion

Generation of carbanions

Lithium transmetalation

Silyl carbanions

Silyl lithium

Silyl transmetalation

Tin-lithium transmetallation

Transmetalation

Transmetalations

Transmetallation

Transmetallations

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