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Anti Cram-Felkin stereochemical control

J. I Cram-Felkin and Anti Cram-Felkin Stereochemical Control... [Pg.661]

The stereochemical outcome of the Mukaiyama reaction can be controlled by the type of Lewis acid used. With bidentate Lewis acids the aldol reaction led to the anti products through a Cram chelate control [366]. Alternatively, the use of a monoden-tate Lewis acid in this reaction led to the syn product through an open Felkin-Anh... [Pg.156]

See other pages where Anti Cram-Felkin stereochemical control is mentioned: [Pg.677] [Pg.677] [Pg.677] [Pg.182] [Pg.183] [Pg.182] [Pg.183] [Pg.182] [Pg.183] [Pg.30]

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Anti-Cram

Felkin

Felkin control

Stereochemical control