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  2. Mozingo reduction - Wikipedia

    en.wikipedia.org/wiki/Mozingo_reduction

    The Mozingo reduction, also known as Mozingo reaction or thioketal reduction, is a chemical reaction capable of fully reducing a ketone or aldehyde to the corresponding alkane via a dithioacetal. [1] [2] The reaction scheme is as follows: [3]

  3. Tsuji–Wilkinson decarbonylation reaction - Wikipedia

    en.wikipedia.org/wiki/Tsuji–Wilkinson...

    In addition to aliphatic, aromatic, and α,β-unsaturated aldehydes, acyl nitriles and 1,2-diketones are also suitable substrates. Few methods exist for decarbonylation. One illustrative application is the synthesis of the core nucleus of FR-900482. [3] Note that the ester is unaffected by the rhodium reagent. Synthetic example of Tsuji ...

  4. McMurry reaction - Wikipedia

    en.wikipedia.org/wiki/McMurry_reaction

    This reductive coupling can be viewed as involving two steps. First is the formation of a pinacolate (1,2-diolate) complex, a step which is equivalent to the pinacol coupling reaction. The second step is the deoxygenation of the pinacolate, which yields the alkene, this second step exploits the oxophilicity of titanium.

  5. Wolff–Kishner reduction - Wikipedia

    en.wikipedia.org/wiki/Wolff–Kishner_reduction

    The Wolff–Kishner reduction is a reaction used in organic chemistry to convert carbonyl functionalities into methylene groups. [1] [2] In the context of complex molecule synthesis, it is most frequently employed to remove a carbonyl group after it has served its synthetic purpose of activating an intermediate in a preceding step.

  6. Reductions with samarium(II) iodide - Wikipedia

    en.wikipedia.org/wiki/Reductions_with_samarium...

    The mechanism of reductions of aldehydes and ketones by samarium(II) iodide is based primarily on mechanisms elucidated for similar one-electron reducing agents. [12] Upon single-electron transfer, a ketyl dimer iv forms. In the absence of protic solvent, this dimer collapses to form 1,2-diols.

  7. Aldehyde dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/Aldehyde_dehydrogenase

    Aldehyde dehydrogenase is a polymorphic enzyme [3] responsible for the oxidation of aldehydes to carboxylic acids. [3] There are three different classes of these enzymes in mammals: class 1 (low K m, cytosolic), class 2 (low K m, mitochondrial), and class 3 (high K m, such as those expressed in tumors, stomach, and cornea). In all three classes ...

  8. Deoxygenation - Wikipedia

    en.wikipedia.org/wiki/Deoxygenation

    Deoxygenation is a chemical reaction involving the removal of oxygen atoms from a molecule. The term also refers to the removal of molecular oxygen (O 2 ) from gases and solvents, a step in air-free technique and gas purifiers .

  9. Carbonyl reduction - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_reduction

    Aldehydes and ketones can be reduced respectively to primary and secondary alcohols. In deoxygenation, the alcohol group can be further reduced and removed altogether by replacement with H. Two broad strategies exist for carbonyl reduction. One method, which is favored in industry, uses hydrogen as the reductant.