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Additions of Chiral Imide Enolates to Michael Acceptors

4-Additions of Chiral Imide Enolates to Michael Acceptors [Pg.564]

The use of homologous acyl derivatives of 153 (i.e., Xc-C(0)Et, Xc-C(0)CH2CH2Ph) would be expected to give higher diastereoselectivities in such Michael additions, as would the use of the Oppolzer sultam analog of 153. namely 1( 0. In cold experiments reportedly [Pg.564]

161 has been proposed as a valuable intermediate for the preparation of carbon-13/14-labeled substituted prolines and 2-hydroxy-piperidones. [Pg.565]

Additions of chiral imide enolates to Michael acceptors ... [Pg.551]



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Addition Acceptors

Addition to enols

Additions to Enolates

Chiral additives

Chiral enolate

Chiral enolate addition

Chiral enolates, Michael additions

Enolate Additions

Enolates Michael

Enolates Michael addition

Enolates chiral

Imide enolates

Imide enolates, chiral

Michael acceptor

Michael addition acceptors

Michael addition of enolate

Michael addition of enolates

Michael additions chiral acceptors

Michael additions imides

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