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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. 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 ...

  4. Dhevalapally B. Ramachary - Wikipedia

    en.wikipedia.org/wiki/Dhevalapally_B._Ramachary

    In 2005, when Ramachary started his own research career at School of Chemistry, UoH, he showed interest towards discovering green reactions and catalysts.His laboratory mainly focused on the development of organocatalytic sequential one-pot reactions, asymmetric supramolecular catalysis and organocatalysis, development of multi-component and multi-catalysis cascade reactions, [9] and metal ...

  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. On-water reaction - Wikipedia

    en.wikipedia.org/wiki/On-water_reaction

    In the context of organocatalysis, both concepts of on-water reactions and in-the-presence-of-water reactions were criticized in 2007 as not so environmentally friendly by Donna Blackmond. According to Blackmond, separation of reaction product from the water phase usually requires organic solvent anyway, and in reported aqueous systems the ...

  9. Photoredox catalysis - Wikipedia

    en.wikipedia.org/wiki/Photoredox_catalysis

    Organocatalysis is a subfield of catalysis that explores the potential of organic small molecules as catalysts, particularly for the enantioselective creation of chiral molecules. One strategy in this subfield is the use of chiral secondary amines to activate carbonyl compounds.

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