In organic chemistry, an imine (/ɪˈmiːn/ or /ˈɪmɪn/) is a functional group or organic compound containing a carbon–nitrogen double bond (C=N). The nitrogen...
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Sydnone imine is a mesoionic heterocyclic aromatic chemical compound. Sydnone imine is the imine of sydnone where the keto functional group of sydnone...
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Methylene imine is an organic compound with the chemical formula H2C=NH. The simplest imine, it is a stable, colorless gas that has been detected throughout...
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An imine reductase (IRED) is an enzyme that reduces imines to amines. This family of enzymes is employed in the industrial production of amine-containing...
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Aza-Diels–Alder reaction (redirect from Imine_Diels–Alder_reaction)
process places the imine lone pair (or coordinated Lewis acid) in an exo position. Thus, (E) imines, in which the lone pair and larger imine carbon substituent...
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imines, being either secondary ketimines or secondary aldimines depending on their structure. Anil refers to a common subset of Schiff bases: imines derived...
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Benzophenone imine is an organic compound with the formula of (C6H5)2C=NH. A pale yellow liquid, benzophenone imine is used as a reagent in organic synthesis...
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determines the rate of reaction. More electron rich imines reduce at faster rates than electron poor imines. The resulting iminium center undergoes nucleophilic...
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Amine (section Conversion to imines)
the production of dyes. Imine formation is an important reaction. Primary amines react with ketones and aldehydes to form imines. In the case of formaldehyde...
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Azetidine (redirect from Trimethylene imine)
Azetidine Systematic IUPAC name Azacyclobutane Other names Azetane Trimethylene imine 1,3-Propylenimine Identifiers CAS Number 503-29-7 Y 3D model (JSmol) Interactive...
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Aziridine (redirect from Ethylene imine)
Aziridine is an organic compound consisting of the three-membered heterocycle C2H5N. It is a colorless, toxic, volatile liquid that is of significant practical...
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Acetone imine, or 2-propanimine is an organic compound and an imine with the chemical formula (CH3)2CNH. It is a volatile and flammable liquid at room...
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involves the conversion of a carbonyl group to an amine via an intermediate imine. The carbonyl group is most commonly a ketone or an aldehyde. It is a common...
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Polyethylenimine (redirect from Poly(ethylene imine))
Polyethylenimine (PEI) or polyaziridine is a polymer with repeating units composed of the amine group and two carbon aliphatic CH2CH2 spacers. Linear polyethyleneimines...
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An imine N-oxide may refer to: An oxime (>C=NOH) A nitrone (>C=N(O)-) This disambiguation page lists articles associated with the title Imine N-oxide....
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any primary or secondary amine to produce resonance stabilized imine (iminium ion or imine salt). The addition of a carbanion from a CH acidic compound...
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NAPQI (redirect from N-acetyl-p-benzo-quinone imine)
NAPQI, also known as NAPBQI or N-acetyl-p-benzoquinone imine, is a toxic byproduct produced during the xenobiotic metabolism of the analgesic paracetamol...
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Covalent organic framework (section Imine condensation)
high temperature (400 °C)). CTF-1 is a good example of this chemistry. The imine condensation reaction which eliminates water (exemplified by reacting aniline...
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Propyleneimine (redirect from Propylene imine)
Propyleneimine (or propylene imine) is the organic compound with the formula CH3CH(NH)CH2. It is a secondary amine and the smallest chiral aziridine (ring...
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of carbon dioxide. An ammonium ion is added forming an imine and releasing ammonia. The imine goes through hydrolysis to form the amine, which is depicted...
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state imine. This strategy was developed by the laboratory Sivaguru and co-workers to overcome the shortcomings involving direct excitation of imines. Traditionally...
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reactivity and spatial properties of the imine, complicating the development of a general catalyst system for imine hydrogenation. Despite these challenges...
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In organic chemistry, an imino acid is any molecule that contains both imine (>C=NH) and carboxyl (-C(=O)-OH) functional groups. Imino acids are structurally...
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In organic chemistry, an oxime is an organic compound belonging to the imines, with the general formula RR’C=N−OH, where R is an organic side-chain and...
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through an intermediate imine. The carbonyl is first treated with ammonia to promote imine formation by nucleophilic attack. The imine is then reduced to an...
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N-Sulfinyl imines (N-sulfinylimines, sulfinimines, thiooxime S-oxides) are a class of imines bearing a sulfinyl group attached to nitrogen. These imines display...
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derived structures such as the nucleobases guanine, thymine, and cytosine imine – imine, e.g., during pyridoxal phosphate catalyzed enzymatic reactions R1R2C(=NCHR3R4)...
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of the amine begins with imine formation with formaldehyde. The formic acid acts as a source of hydride and reduces the imine to a secondary amine. Loss...
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the unsubstituted porphine; D, a mixed amine/imine, the Curtis macrocycle; E, the related enamine/imine Jäger macrocycle, and F, the tetracarboxylate-derivative...
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Polyimine (category Imines)
Polyimines are classified as polymer materials that contain imine groups, which are characterised by a double bond between a carbon and nitrogen atom...
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