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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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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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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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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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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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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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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