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Amination information


Amination is the process by which an amine group is introduced into an organic molecule. This type of reaction is important because organonitrogen compounds are pervasive.

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Amination

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Amination is the process by which an amine group is introduced into an organic molecule. This type of reaction is important because organonitrogen compounds...

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Reductive amination

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Reductive amination (also known as reductive alkylation) is a form of amination that involves the conversion of a carbonyl group to an amine via an intermediate...

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Chichibabin reaction

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The following is the overall form of the general reaction: The direct amination of pyridine with sodium amide takes place in liquid ammonia. Following...

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Electrophilic amination

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Electrophilic amination is a chemical process involving the formation of a carbon–nitrogen bond through the reaction of a nucleophilic carbanion with...

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Transamination

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Transamination is a chemical reaction that transfers an amino group to a ketoacid to form new amino acids.This pathway is responsible for the deamination...

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Deamination

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Deamination is the removal of an amino group from a molecule. Enzymes that catalyse this reaction are called deaminases. In the human body, deamination...

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Acyloin

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Bruyn–van Ekenstein transformation A similar reaction is the so-called Voigt amination where an acyloin reacts with a primary amine and phosphorus pentoxide...

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Hydroquinone

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Hydroquinone, also known as benzene-1,4-diol or quinol, is an aromatic organic compound that is a type of phenol, a derivative of benzene, having the chemical...

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Sodium triacetoxyborohydride

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aldehydes but not most ketones. It is especially suitable for reductive aminations of aldehydes and ketones. However, unlike sodium cyanoborohydride, the...

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MDMA

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catalyst. Once the MDP2P intermediate has been prepared, a reductive amination leads to racemic MDMA (an equal parts mixture of (R)-MDMA and (S)-MDMA)...

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Ammonium formate

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hydrogens (hydrogenolysis). Ammonium formate can be used for reductive amination of aldehydes and ketones (Leuckart reaction), by the following reaction:...

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Leuckart reaction

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chemical reaction that converts aldehydes or ketones to amines by reductive amination in the presence of heat. The reaction, named after Rudolf Leuckart, uses...

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Amine alkylation

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often limited to the synthesis of tertiary amines. An exception is the amination of alpha-halo carboxylic acids that do permit synthesis of primary amines...

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Amino acid

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This process involves transaminases, often the same as those used in amination during synthesis. In many vertebrates, the amino group is then removed...

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Amine

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scale. Many amines are produced from aldehydes and ketones via reductive amination, which can either proceed catalytically or stoichiometrically. Aniline...

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XPhos

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biphenyl. Its palladium complexes exhibit high activity for Buchwald-Hartwig amination reactions involving aryl chlorides and aryl tosylates. Both palladium...

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Methamphetamine

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prepared starting from phenylacetone by either the Leuckart or reductive amination methods. In the Leuckart reaction, one equivalent of phenylacetone is...

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Aminonaphthalenesulfonic acids

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acid Bucherer amination of 2-hydroxynaphthalene-7-sulfonic acid 2-Aminonaphthalene-8-sulfonic acid 86-60-2 Badische acid Bucherer amination of...

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Imine reductase

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from ketone-amine mixtures. The conversion is not a genuine reductive amination as only the second half of the two-part reaction is catalyzed. In 2017...

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Carbonyl reduction

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alcohols, aldehydes and ketones can be converted to amines, i.e., reductive amination. Because of its cyano substituent, NaBH3CN is a weak reducer at moderate...

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Lithium

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Luo (1986). "Functionalization of polymeric organolithium compounds. Amination of poly(styryl)lithium". Macromolecules. 19 (5): 1291–1294. Bibcode:1986MaMol...

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Glycine

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manufactured more conveniently by chemical synthesis. The two main processes are amination of chloroacetic acid with ammonia, giving glycine and ammonium chloride...

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White catalyst

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catalyst can effect both branched and linear regioselective allylic C-H aminations. In order to promote nucleophilic attack at the internal terminus of the...

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Solanine

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Solanaceae plants: Involvement of an aldehyde intermediate during C-26 amination". Phytochemistry. 89: 26–31. Bibcode:2013PChem..89...26O. doi:10.1016/j...

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Valine

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leads to leucine. The intermediate α-ketoisovalerate undergoes reductive amination with glutamate. Enzymes involved in this biosynthesis include: Acetolactate...

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