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  2. Decarboxylation - Wikipedia

    en.wikipedia.org/wiki/Decarboxylation

    In beverages stored for long periods, very small amounts of benzene may form from benzoic acid by decarboxylation catalyzed by the presence of ascorbic acid. [15] The addition of catalytic amounts of cyclohexenone has been reported to catalyze the decarboxylation of amino acids. [16]

  3. N-Bromosuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Bromosuccinimide

    1 Preparation. 2 Reactions. Toggle Reactions subsection. 2.1 Addition to alkenes. 2.2 Allylic and benzylic bromination. ... Oxidative decarboxylation of α-amino acids

  4. Akabori amino-acid reaction - Wikipedia

    en.wikipedia.org/wiki/Akabori_amino-acid_reaction

    There are several Akabori amino acid reactions, which are named after Shirō Akabori (Japanese: 赤堀 四郎) (1900–1992), a Japanese chemist. In the first reaction, an α- amino acid is oxidised and undergoes decarboxylation to give an aldehyde at the former α position by heating with oxygen in the presence of a reducing sugar .

  5. Erlenmeyer–Plöchl azlactone and amino-acid synthesis

    en.wikipedia.org/wiki/Erlenmeyer–Plöchl...

    The Erlenmeyer–Plöchl azlactone and amino acid synthesis, named after Friedrich Gustav Carl Emil Erlenmeyer who partly discovered the reaction, is a series of chemical reactions which transform an N-acyl glycine to various other amino acids via an oxazolone (also known as an azlactone). [1] [2] Azlactone chemistry: step 2 is a Perkin variation

  6. Biogenic amine - Wikipedia

    en.wikipedia.org/wiki/Biogenic_amine

    They are basic nitrogenous compounds formed mainly by decarboxylation of amino acids or by amination and transamination of aldehydes and ketones. Biogenic amines are organic bases with low molecular weight and are synthesized by microbial, vegetable and animal metabolisms. In food and beverages they are formed by the enzymes of raw material or ...

  7. Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Schmidt_reaction

    In organic chemistry, the Schmidt reaction is an organic reaction in which an azide reacts with a carbonyl derivative, usually an aldehyde, ketone, or carboxylic acid, under acidic conditions to give an amine or amide, with expulsion of nitrogen.

  8. Kolbe electrolysis - Wikipedia

    en.wikipedia.org/wiki/Kolbe_electrolysis

    Another example is the synthesis of 2,7-dimethyl-2,7-dinitrooctane from 4-methyl-4-nitrovaleric acid: [3] The Kolbe reaction has also been occasionally used in cross-coupling reactions . In 2022, it was discovered that the Kolbe electrolysis is enhanced if an alternating square wave current is used instead of a direct current .

  9. Reductive amination - Wikipedia

    en.wikipedia.org/wiki/Reductive_amination

    In biochemistry, dehydrogenase enzymes can catalyze the reductive amination of α-keto acids and ammonia to yield α-amino acids. Reductive amination is predominantly used for the synthesis of the amino acid glutamate starting from α-ketoglutarate, while biochemistry largely relies on transamination to introduce nitrogen in the other amino ...