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  2. Enders SAMP/RAMP hydrazone-alkylation reaction - Wikipedia

    en.wikipedia.org/wiki/Enders_SAMP/RAMP_hydrazone...

    The Enders SAMP/RAMP hydrazone alkylation reaction is an asymmetric carbon-carbon bond formation reaction facilitated by pyrrolidine chiral auxiliaries. It was pioneered by E. J. Corey and Dieter Enders in 1976, [1] and was further developed by Enders and his group. [2] This method is usually a three-step sequence.

  3. Kinetic resolution - Wikipedia

    en.wikipedia.org/wiki/Kinetic_resolution

    The Noyori asymmetric hydrogenation of ketones is an excellent example of dynamic kinetic resolution at work. The enantiomeric β-ketoesters can undergo epimerization , and the choice of chiral catalyst, typically of the form Ru[(R)-BINAP]X 2 , where X is a halogen , leads to one of the enantiomers reacting preferentially faster.

  4. Depletion force - Wikipedia

    en.wikipedia.org/wiki/Depletion_force

    This method is used to find depletion force strength by adhering to a static plate one particle in a dispersion particle doublet and applying shear force through fluid flow. The drag created by the dispersion particles resists the depletion force between them, pulling the free particle away from the adhered particle. A force balance of the ...

  5. Asymmetric hydrogenation - Wikipedia

    en.wikipedia.org/wiki/Asymmetric_hydrogenation

    Iron is a popular research target for many catalytic processes, owing largely to its low cost and low toxicity relative to other transition metals. [18] Asymmetric hydrogenation methods using iron have been realized, although in terms of rates and selectivity, they are inferior to catalysts based on precious metals. [19]

  6. 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).

  7. 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."

  8. Baylis–Hillman reaction - Wikipedia

    en.wikipedia.org/wiki/Baylis–Hillman_reaction

    For example, chiral phosphines containing a Lewis base, a Bronsted acid, and an acid-activated Bronsted base were developed for an asymmetric aza-MBH reaction (86-96% yield, 79-92% ee). The Bronsted acid and base moieties were proposed to be involved in the stabilization of zwitterionic species in a stereoselective manner.

  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 ...