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The mechanism for base-catalyzed aldol condensation can be seen in the image below. A mechanism for aldol condensation in basic conditions, which occurs via enolate intermediates and E1CB elimination. The process begins when a free hydroxide (strong base) strips the highly acidic proton at the alpha carbon of the aldehyde.
The aldol itself is then formed, and it may then undergo dehydration to give the unsaturated carbonyl compound. The scheme shows a simple mechanism for the base-catalyzed aldol reaction of an aldehyde with itself. Simple mechanism for base-catalyzed aldol reaction of an aldehyde with itself
After which it may undergo dehydration to give a unsaturated carbonyl compound, the aldol condensation product. The scheme shows a simple mechanism for the base-catalyzed aldol reaction of an aldehyde with itself. Base-catalyzed aldol reaction. Simple mechanism for base-catalyzed aldol reaction of an aldehyde with itself. Base-catalyzed dehydration
The Hajos–Parrish–Eder–Sauer–Wiechert and Barbas-List [1] reactions in organic chemistry are a family of proline-catalysed asymmetric aldol reactions.. In the 1970s, two research groups discovered (and published) almost simultaneously their discoveries of two related intramolecular reactions: Zoltan Hajos and David Parrish at Hoffmann-La Roche [2] [3] and Rudolf Wiechert et al at ...
Aldol reactions are a key reaction in organic chemistry because they provide a means of forming carbon-carbon bonds, allowing for the synthesis of more complex molecules. [9] An aldol condensation reaction is one of the most common examples of an E1cB mechanism.
Similar to many other organic bases, DBN could be employed for dehydrohalogenation reactions, base-catalyzed rearrangement reactions, as well as Aldol condensation. [3] Several examples are shown below: Elimination: [2] Epimerization of penicillin derivatives, catalyzed by DBN: [4] Aldol condensation: [5]
Idealized scheme showing condensation of two amino acids to give a peptide bond. Many variations of condensation reactions exist. Common examples include the aldol condensation and the Knoevenagel condensation , which both form water as a by-product, as well as the Claisen condensation and the Dieckman condensation (intramolecular Claisen ...
These two steps are similar to a base-catalyzed aldol reaction. The oxygen anion in this aldol-like product then S N 2 attacks on the formerly-nucleophilic halide-bearing position, displacing the halide to form an epoxide. [2] This reaction sequence is thus a condensation reaction since there is a net loss of HCl when the two reactant molecules ...