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Michael condensation, between diethyl

Michael condensation, between diethyl malonate and methyl crotonate, 38, 53... [Pg.53]

Frequently the basic conditions used cause the initial Michael adduct to undergo intramolecular transformations, as for example in the synthesis of dimedone (Expt 7.11). This involves a Michael reaction between mesityl oxide and diethyl malonate followed by an internal Claisen ester condensation. [Pg.681]

See other pages where Michael condensation, between diethyl is mentioned: [Pg.197]    [Pg.229]    [Pg.464]    [Pg.464]    [Pg.309]    [Pg.123]    [Pg.318]    [Pg.84]   


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Michael condensation

Michael condensation, between diethyl malonate and methyl crotonate

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