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  2. Organic reaction - Wikipedia

    en.wikipedia.org/wiki/Organic_reaction

    Organic chemistry has a strong tradition of naming a specific reaction to its inventor or inventors and a long list of so-called named reactions exists, conservatively estimated at 1000. A very old named reaction is the Claisen rearrangement (1912) and a recent named reaction is the Bingel reaction (1993).

  3. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Algar–Flynn–Oyamada reaction; Alkylimino-de-oxo-bisubstitution; Alkyne trimerisation; Alkyne zipper reaction; Allan–Robinson reaction; Allylic rearrangement; Amadori rearrangement; Amine alkylation; Angeli–Rimini reaction; Andrussov oxidation; Appel reaction; Arbuzov reaction, Arbusow reaction; Arens–Van Dorp synthesis, Isler ...

  4. Name reaction - Wikipedia

    en.wikipedia.org/wiki/Name_reaction

    Although systematic approaches for naming reactions based on the reaction mechanism or the overall transformation exist, such as the IUPAC nomenclature for organic chemical transformations, these technically-descriptive names are often unwieldy or not specific enough, so people names are often more practical for efficient communication. [5]

  5. Passerini reaction - Wikipedia

    en.wikipedia.org/wiki/Passerini_reaction

    Proposed concerted version of the Passerini reaction mechanism. This mechanism involves a trimolecular reaction between the isocyanide, carboxylic acid, and carbonyl in a sequence of nucleophilic additions. The reaction proceeds first through an imidate intermediate and then undergoes Mumm rearrangement to afford the Passerini product. [13] [14]

  6. Fractionation of carbon isotopes in oxygenic photosynthesis

    en.wikipedia.org/wiki/Fractionation_of_carbon...

    A simplified model of a chemical reaction with pathways for a light isotope (H) and heavy isotope (D) of hydrogen. The same principle applies for the light isotope 12 C and heavy isotope 13 C of carbon. The positions on the energy wells are based on the quantum harmonic oscillator. Note the lower energy state of the heavier isotope and the ...

  7. Crassulacean acid metabolism - Wikipedia

    en.wikipedia.org/wiki/Crassulacean_acid_metabolism

    During the night, a plant employing CAM has its stomata open, allowing CO 2 to enter and be fixed as organic acids by a PEP reaction similar to the C 4 pathway. The resulting organic acids are stored in vacuoles for later use, as the Calvin cycle cannot operate without ATP and NADPH, products of light-dependent reactions that do not take place ...

  8. IUPAC nomenclature for organic chemical transformations

    en.wikipedia.org/wiki/IUPAC_nomenclature_for...

    The IUPAC Nomenclature for Organic Chemical Transformations is a methodology for naming a chemical reaction.. Traditionally, most chemical reactions, especially in organic chemistry, are named after their inventors, the so-called name reactions, such as Knoevenagel condensation, Wittig reaction, Claisen–Schmidt condensation, Schotten–Baumann reaction, and Diels–Alder reaction.

  9. Photosynthesis - Wikipedia

    en.wikipedia.org/wiki/Photosynthesis

    Some plants have evolved mechanisms to increase the CO 2 concentration in the leaves under these conditions. [ 30 ] Plants that use the C 4 carbon fixation process chemically fix carbon dioxide in the cells of the mesophyll by adding it to the three-carbon molecule phosphoenolpyruvate (PEP), a reaction catalyzed by an enzyme called PEP ...