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  2. Organocatalysis - Wikipedia

    en.wikipedia.org/wiki/Organocatalysis

    In organic chemistry, organocatalysis is a form of catalysis in which the rate of a chemical reaction is increased by an organic catalyst. This "organocatalyst" consists of carbon , hydrogen , sulfur and other nonmetal elements found in organic compounds.

  3. Thiourea organocatalysis - Wikipedia

    en.wikipedia.org/wiki/Thiourea_organocatalysis

    Within the area of organocatalysis, (thio)urea organocatalysis describes the use of ureas and thioureas to accelerate and stereochemically alter organic transformations. The effects arise through hydrogen-bonding interactions between the substrate and the (thio)urea.

  4. Catalysis - Wikipedia

    en.wikipedia.org/wiki/Catalysis

    The discipline organocatalysis is divided into the application of covalent (e.g., proline, DMAP) and non-covalent (e.g., thiourea organocatalysis) organocatalysts referring to the preferred catalyst-substrate binding and interaction, respectively. The Nobel Prize in Chemistry 2021 was awarded jointly to Benjamin List and David W.C. MacMillan ...

  5. Hydrogen-bond catalysis - Wikipedia

    en.wikipedia.org/wiki/Hydrogen-bond_catalysis

    Hydrogen-bond catalysis is a type of organocatalysis that relies on use of hydrogen bonding interactions to accelerate and control organic reactions. In biological systems, hydrogen bonding plays a key role in many enzymatic reactions, both in orienting the substrate molecules and lowering barriers to reaction. [1]

  6. N-Heterocyclic olefins - Wikipedia

    en.wikipedia.org/wiki/N-heterocyclic_olefins

    Unsaturated NHO. An N-heterocyclic olefin (NHO) is a neutral heterocyclic compound with a highly polarized, electron-rich C=C olefin attached to a heterocycle made up of two nitrogen atoms.

  7. Proline organocatalysis - Wikipedia

    en.wikipedia.org/wiki/Proline_organocatalysis

    Proline organocatalysis is the use of proline as an organocatalyst in organic chemistry. This theme is often considered the starting point for the area of organocatalysis, even though early discoveries went unappreciated. [1] Modifications, such as MacMillan’s catalyst and Jorgensen's catalysts, proceed with excellent stereocontrol. [2]: 5574 [3]

  8. Thiourea - Wikipedia

    en.wikipedia.org/wiki/Thiourea

    Thiourea (/ ˌ θ aɪ. oʊ j ʊəˈr iː. ə,-ˈ jʊər i-/) [2] [3] [4] is an organosulfur compound with the formula SC(NH 2) 2 and the structure H 2 N−C(=S)−NH 2.It is structurally similar to urea (H 2 N−C(=O)−NH 2), except that the oxygen atom is replaced by a sulfur atom (as implied by the thio-prefix); however, the properties of urea and thiourea differ significantly.

  9. Category:Catalysis - Wikipedia

    en.wikipedia.org/wiki/Category:Catalysis

    C. Carbocatalysis; Catalase; Catalysis; Catalyst poisoning; Catalytic combustion; Catalytic converter; Catalytic cycle; Catalytic oxidation; Catalytic resonance theory