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  2. Claisen condensation - Wikipedia

    en.wikipedia.org/wiki/Claisen_condensation

    The Claisen condensation is a carbon–carbon bond forming reaction that occurs between two esters or one ester and another carbonyl compound in the presence of a strong base. The reaction produces a β-keto ester or a β-diketone. [1] It is named after Rainer Ludwig Claisen, who first published his work on the reaction in 1887.

  3. Claisen rearrangement - Wikipedia

    en.wikipedia.org/wiki/Claisen_rearrangement

    The Claisen rearrangement is a powerful carbon–carbon bond-forming chemical reaction discovered by Rainer Ludwig Claisen. [1] The heating of an allyl vinyl ether will initiate a [3,3]-sigmatropic rearrangement to give a γ,δ-unsaturated carbonyl, driven by exergonically favored carbonyl CO bond formation (Δ(Δ f H) = −327 kcal/mol (−1,370 kJ/mol).

  4. 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 ...

  5. Rainer Ludwig Claisen - Wikipedia

    en.wikipedia.org/wiki/Rainer_Ludwig_Claisen

    The reaction is known as the Claisen reaction and was described by Claisen for the first time in 1890. Discovered the thermally induced rearrangement of allyl phenyl ether in 1912. He details its reaction mechanism in his last scientific publication (1925). In his honor, the reaction has been named the Claisen rearrangement.

  6. Aldol condensation - Wikipedia

    en.wikipedia.org/wiki/Aldol_condensation

    Aldol condensation. An aldol condensation is a condensation reaction in organic chemistry in which two carbonyl moieties (of aldehydes or ketones) react to form a β-hydroxyaldehyde or β-hydroxyketone (an aldol reaction), and this is then followed by dehydration to give a conjugated enone. The overall reaction equation is as follows (where the ...

  7. Rearrangement reaction - Wikipedia

    en.wikipedia.org/wiki/Rearrangement_reaction

    A pericyclic reaction is a type of reaction with multiple carbon–carbon bond making and breaking wherein the transition state of the molecule has a cyclic geometry, and the reaction progresses in a concerted fashion. Examples are hydride shifts. and the Claisen rearrangement: [5]

  8. Ortho ester - Wikipedia

    en.wikipedia.org/wiki/Ortho_ester

    The general formula of orthoesters. In organic chemistry, an ortho ester is a functional group containing three alkoxy groups attached to one carbon atom, i.e. with the general formula RC (OR')3. Orthoesters may be considered as products of exhaustive alkylation of unstable orthocarboxylic acids and it is from these that the name 'ortho ester ...

  9. 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 ...