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Specific enol equivalents from 1,3-dicarbonyl compounds... [Pg.702]

We met enamines as specific enol equivalents in the last chapter and they are particularly good at conjugate addition. The pyrrolidine enamine from cyclohexanone 41 adds to acrylic esters 42 in conjugate fashion and the first-formed product 43 gives the enamine 44 by proton exchange.4 Acid hydrolysis via the imine salt 45 gives the 1,5-dicarbonyl compound 46. [Pg.154]

See other pages where Specific enol equivalents from 1,3-dicarbonyl compounds is mentioned: [Pg.38] [Pg.39]