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Robinson annulation, synthetic methods

Robinson annulation (Section 18.13) The combination of a Michael addition and an intramolecular aldol condensation used as a synthetic method for ring formation. [Pg.1293]

The reactions described in this chapter include some of the most useful synthetic methods for carbon-carbon bond formation the aldol and Claisen condensations, the Robinson annulation, and the Wittig reaction and related olefination methods. All of these reactions begin by the addition of a carbon nucleophile to a carbonyl group. The product which is isolated depends on the nature of the substituent (X) on the carbon nucleophile, the substituents (A and B) on the carbonyl group, and the ways in which A, B, and X interact to control the reaction pathways available to the addition intermediate. [Pg.57]


See other pages where Robinson annulation, synthetic methods is mentioned: [Pg.23]    [Pg.483]    [Pg.63]    [Pg.33]    [Pg.2]    [Pg.24]    [Pg.113]    [Pg.130]    [Pg.156]    [Pg.288]    [Pg.130]    [Pg.30]   
See also in sourсe #XX -- [ Pg.190 , Pg.191 ]




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Robinson annulation

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