Enolate Ions and Reactions Alpha to Carbonyl in Organic Chemistry
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Enolate Ions and Reactions Alpha to Carbonyl in Organic Chemistry
Organic Chemistry Tutorial Series involving enolate ions and reactions at the alpha carbonyl position including Aldol, Claisen, Dieckmann condensations, Malonic and Acetoacetic Ester synthesis and more.
Mar 10, 2022
Enolate Reactions
The Claisen condensation enables the base-promoted formation of β-keto esters from esters bearing α-hydrogens, forging new C–C bonds through enolate attack on an ester carbonyl. Developed by Rainer Ludwig Claisen in the late 19th century, the reaction proceeds through ester enolate formation, carbon–carbon bond formation between two ester units, and subsequent acidic workup to yield the β-dicarbonyl product. Learn. Review. Repeat.
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The Claisen condensation enables the base-promoted formation of β-keto esters from esters bearing α-hydrogens, forging new C–C bonds through enolate attack on an ester carbonyl. Developed by Rainer Ludwig Claisen in the late 19th century, the reaction proceeds through ester enolate formation, carbon–carbon bond formation between two ester units, and subsequent acidic workup to yield the β-dicarbonyl product. Learn. Review. Repeat.
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