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  2. Aldol condensation - Wikipedia

    en.wikipedia.org/wiki/Aldol_condensation

    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.

  3. Aldol reaction - Wikipedia

    en.wikipedia.org/wiki/Aldol_reaction

    The aldol reaction (aldol addition) is a reaction in organic chemistry that combines two carbonyl compounds (e.g. aldehydes or ketones) to form a new β-hydroxy carbonyl compound. Its simplest form might involve the nucleophilic addition of an enolized ketone to another: These products are known as aldols, from the ald ehyde + alcoh ol, a ...

  4. Henry reaction - Wikipedia

    en.wikipedia.org/wiki/Henry_reaction

    Henry reaction. The Henry reaction is a classic carbon–carbon bond formation reaction in organic chemistry. Discovered in 1895 by the Belgian chemist Louis Henry (1834–1913), it is the combination of a nitroalkane and an aldehyde or ketone in the presence of a base to form β-nitro alcohols. [1][2][3] This type of reaction is also referred ...

  5. Claisen–Schmidt condensation - Wikipedia

    en.wikipedia.org/wiki/Claisen–Schmidt_condensation

    Claisen–Schmidt condensation. In organic chemistry, the Claisen–Schmidt condensation is the reaction between an aldehyde or ketone having an α-hydrogen with an aromatic carbonyl compound lacking an α-hydrogen. It can be considered as a specific variation of the aldol condensation. This reaction is named after two of its pioneering ...

  6. Citrate synthase - Wikipedia

    en.wikipedia.org/wiki/Citrate_synthase

    Citrate synthase (E.C. 2.3.3.1 (previously 4.1.3.7)) is an enzyme that exists in nearly all living cells. It functions as a pace-making enzyme in the first step of the citric acid cycle (or Krebs cycle). [ 5 ] Citrate synthase is located within eukaryotic cells in the mitochondrial matrix, but is encoded by nuclear DNA rather than mitochondrial ...

  7. Proline-catalyzed aldol reactions - Wikipedia

    en.wikipedia.org/wiki/Proline-catalyzed_aldol...

    Proline-catalyzed aldol reactions. 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 ...

  8. Condensation reaction - Wikipedia

    en.wikipedia.org/wiki/Condensation_reaction

    Condensation reaction. In organic chemistry, a condensation reaction is a type of chemical reaction in which two molecules are combined to form a single molecule, usually with the loss of a small molecule such as water. [1] If water is lost, the reaction is also known as a dehydration synthesis. However other molecules can also be lost, such as ...

  9. Fructose-bisphosphate aldolase - Wikipedia

    en.wikipedia.org/wiki/Fructose-bisphosphate_aldolase

    Fructose-bisphosphate aldolase (EC 4.1.2.13), often just aldolase, is an enzyme catalyzing a reversible reaction that splits the aldol, fructose 1,6-bisphosphate, into the triose phosphates dihydroxyacetone phosphate (DHAP) and glyceraldehyde 3-phosphate (G3P). Aldolase can also produce DHAP from other (3S,4R)- ketose 1-phosphates such as ...