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  2. Non-linear effects - Wikipedia

    en.wikipedia.org/wiki/Non-linear_effects

    It is often referred to as asymmetric amplification, a term coined by Oguni and co-workers. [4] An example of a positive non-linear effect is observed in the case of Sharpless epoxidation with the substrate geraniol.In all cases of chemical reactivity exhibiting (+)-NLE, there is an innate tradeoff between overall reaction rate and ...

  3. Enantioselective synthesis - Wikipedia

    en.wikipedia.org/wiki/Enantioselective_synthesis

    Enantioselective synthesis, also called asymmetric synthesis, [1] is a form of chemical synthesis.It is defined by IUPAC as "a chemical reaction (or reaction sequence) in which one or more new elements of chirality are formed in a substrate molecule and which produces the stereoisomeric (enantiomeric or diastereomeric) products in unequal amounts."

  4. Dynamic kinetic resolution in asymmetric synthesis - Wikipedia

    en.wikipedia.org/wiki/Dynamic_Kinetic_Resolution...

    Asymmetric synthesis has become a much explored field due to the challenge of creating a compound with a single 3D structure. [1] Even more challenging is the ability to take a racemic mixture and have only one chiral product left after a reaction. One method that has become an exceedingly useful tool is dynamic kinetic resolution (DKR).

  5. Desymmetrization - Wikipedia

    en.wikipedia.org/wiki/Desymmetrization

    PhC(O)C(O)Ph + H 2 → PhCH(OH)C(O)Ph (Ph = C 6 H 5) The precursor benzil has C 2v symmetry, and the product is C 2 symmetric. Citric acid is also a symmetric molecule that can be desymmetrized by partial methylation. Desymmetrization of citric acid. The alcoholysis of cyclic anhydrides can be conducted enantiosymmetrically using chiral amine ...

  6. Corey–Itsuno reduction - Wikipedia

    en.wikipedia.org/wiki/Corey–Itsuno_reduction

    [2] [3] The CBS reduction has since been utilized by organic chemists as a reliable method for the asymmetric reduction of achiral ketones. Notably, it has found prominent use not only in a number of natural product syntheses, but has been utilized on large scale in industry (See Scope Below). Several reviews have been published. [4] [5] [6]

  7. Sharpless asymmetric dihydroxylation - Wikipedia

    en.wikipedia.org/wiki/Sharpless_asymmetric_di...

    The reaction mechanism of the Sharpless dihydroxylation begins with the formation of the osmium tetroxide – ligand complex (2). A [3+2]-cycloaddition with the alkene (3) gives the cyclic intermediate 4. [9] [10] Basic hydrolysis liberates the diol (5) and the reduced osmate (6).

  8. Kinetic resolution - Wikipedia

    en.wikipedia.org/wiki/Kinetic_resolution

    Kinetic resolution is a possible method for irreversibly differentiating a pair of enantiomers due to (potentially) different activation energies. While both enantiomers are at the same Gibbs free energy level by definition, and the products of the reaction with both enantiomers are also at equal levels, the Δ G ‡ {\displaystyle \Delta G ...

  9. Curtin–Hammett principle - Wikipedia

    en.wikipedia.org/wiki/Curtin–Hammett_principle

    The Curtin–Hammett principle is a principle in chemical kinetics proposed by David Yarrow Curtin and Louis Plack Hammett.It states that, for a reaction that has a pair of reactive intermediates or reactants that interconvert rapidly (as is usually the case for conformational isomers), each going irreversibly to a different product, the product ratio will depend both on the difference in ...

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