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Alkylation of Enolates and Other Carbon Nucleophiles

These reactions introduce a new substituent a to the carbonyl group and constitute an important method for this transformation. In the retrosynthetic sense, the disconnection is between the a-carbon and a potential alkylating agent. [Pg.1]

There are similar reactions involving nitrogen analogs called imine anions. The alkylated imines can be hydrolyzed to the corresponding ketone, and this reaction is discussed in Section 1.3. [Pg.2]

See other pages where Alkylation of Enolates and Other Carbon Nucleophiles is mentioned: [Pg.1] [Pg.2] [Pg.4] [Pg.6] [Pg.12] [Pg.14] [Pg.16] [Pg.18] [Pg.20] [Pg.22] [Pg.24] [Pg.26] [Pg.30] [Pg.32] [Pg.34] [Pg.36] [Pg.38] [Pg.40] [Pg.42] [Pg.44] [Pg.46] [Pg.48] [Pg.50] [Pg.52] [Pg.54] [Pg.56] [Pg.58] [Pg.60]