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Leuckart reaction

Index Leuckart reaction

The Leuckart reaction is the chemical reaction that converts aldehydes or ketones to amines by reductive amination in the presence of heat. [1]

18 relations: Amine, Ammonia, Ammonium formate, Benzaldehyde, Benzodiazepine, Benzylamine, Carbonyl group, Catalysis, Chemical reaction, Eschweiler–Clarke reaction, Formamide, Formic acid, Ketone, Nucleophile, Reducing agent, Reductive amination, Rudolf Leuckart (chemist), Solid-phase synthesis.

Amine

In organic chemistry, amines are compounds and functional groups that contain a basic nitrogen atom with a lone pair.

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Ammonia

Ammonia is a compound of nitrogen and hydrogen with the formula NH3.

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Ammonium formate

Ammonium formate, NH4HCO2, is the ammonium salt of formic acid.

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Benzaldehyde

Benzaldehyde (C6H5CHO) is an organic compound consisting of a benzene ring with a formyl substituent.

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Benzodiazepine

Benzodiazepines (BZD, BZs), sometimes called "benzos", are a class of psychoactive drugs whose core chemical structure is the fusion of a benzene ring and a diazepine ring.

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Benzylamine

Benzylamine is an organic chemical compound with the condensed structural formula C6H5CH2NH2 (sometimes abbreviated as PhCH2NH2 or BnNH2).

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Carbonyl group

In organic chemistry, a carbonyl group is a functional group composed of a carbon atom double-bonded to an oxygen atom: C.

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Catalysis

Catalysis is the increase in the rate of a chemical reaction due to the participation of an additional substance called a catalysthttp://goldbook.iupac.org/C00876.html, which is not consumed in the catalyzed reaction and can continue to act repeatedly.

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Chemical reaction

A chemical reaction is a process that leads to the transformation of one set of chemical substances to another.

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Eschweiler–Clarke reaction

The Eschweiler–Clarke reaction (also called the Eschweiler–Clarke methylation) is a chemical reaction whereby a primary (or secondary) amine is methylated using excess formic acid and formaldehyde.

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Formamide

Formamide, also known as methanamide, is an amide derived from formic acid.

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Formic acid

Formic acid, systematically named methanoic acid, is the simplest carboxylic acid.

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Ketone

In chemistry, a ketone (alkanone) is an organic compound with the structure RC(.

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Nucleophile

Nucleophile is a chemical species that donates an electron pair to an electrophile to form a chemical bond in relation to a reaction.

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Reducing agent

A reducing agent (also called a reductant or reducer) is an element (such as calcium) or compound that loses (or "donates") an electron to another chemical species in a redox chemical reaction.

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Reductive amination

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 imine.

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Rudolf Leuckart (chemist)

Carl Louis Rudolf Alexander Leuckart (June 23, 1854 – July 24, 1889) was a German chemist who discovered the Leuckart reaction and Leuckart thiophenol reaction.

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Solid-phase synthesis

In chemistry, solid-phase synthesis is a method in which molecules are bound on a bead and synthesized step-by-step in a reactant solution; compared with normal synthesis in a liquid state, it is easier to remove excess reactant or byproduct from the product.

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Redirects here:

Leuckart-Wallach reaction, Leuckart–Wallach reaction.

References

[1] https://en.wikipedia.org/wiki/Leuckart_reaction

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