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  2. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    Demethylation (the transfer of the methyl group to another compound) is a common process, and reagents that undergo this reaction are called methylating agents. Common methylating agents are dimethyl sulfate, methyl iodide, and methyl triflate. Methanogenesis, the source of natural gas, arises via a demethylation reaction. [8]

  3. Hydrogen auto-transfer - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_auto-transfer

    [1] [2] Mechanism of one type of carbonyl addition hydrogen auto-transfer reaction involving hydrometalation (step 2). [3] Hydrogen auto-transfer, also known as borrowing hydrogen, is the activation of a chemical reaction by temporary transfer of two hydrogen atoms from the reactant to a catalyst and return of those hydrogen atoms back to a ...

  4. Suzuki reaction - Wikipedia

    en.wikipedia.org/wiki/Suzuki_reaction

    The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide. [1] [2] [3] It was first published in 1979 by Akira Suzuki, and he shared the 2010 Nobel Prize in Chemistry with Richard F. Heck and Ei-ichi Negishi for their contribution to the discovery and development of noble metal catalysis in organic ...

  5. Alkynylation - Wikipedia

    en.wikipedia.org/wiki/Alkynylation

    Several modifications of alkynylation reactions are known: In the Arens–van Dorp synthesis the compound ethoxyacetylene [7] is converted to a Grignard reagent and reacted with a ketone, the reaction product is a propargyl alcohol.

  6. Methenium - Wikipedia

    en.wikipedia.org/wiki/Methenium

    In organic chemistry, methenium (also called methylium, carbenium, [2] methyl cation, or protonated methylene) is a cation with the formula CH + 3.It can be viewed as a methylene radical (: CH

  7. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    Cross-couplings are a subset of the more general coupling reactions. Often cross-coupling reactions require metal catalysts. One important reaction type is this: R−M + R'−X → R−R' + MX (R, R' = organic fragments, usually aryl; M = main group center such as Li or MgX; X = halide) These reactions are used to form carbon–carbon bonds but ...

  8. β-Hydride elimination - Wikipedia

    en.wikipedia.org/wiki/Beta-Hydride_elimination

    The geometry of the alkaline product is significant as it dictates further reactions and the mechanism's overall outcome. 4) Regeneration of the Catalyst After the formation of the alkene, the released metal hydride, can either re-enter the catalytic cycle to react with another substrate or be further modified through subsequent reactions. This ...

  9. Carbon–hydrogen bond activation - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond...

    One approach to improving chemical reactions is the understanding of the underlying reaction mechanism. time-resolved spectroscopic techniques can be used to follow the dynamics of the chemical reaction. This technique requires a trigger for initiating the process, which is in most cases illumination of the compound.