imine


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Related to imine: Schiff base

imine

 [ĭ-mēn´]
an organic compound containing an imino group.

imine

(ĭ-mēn´) an organic compound containing an imino group; in a substituted imine, a nonacyl group replaces the imino hydrogen.
References in periodicals archive ?
Synthesis, decomposition kinetics, and preliminary toxicological studies of pure N-acetyl-p-benzoquinone imine, a proposed toxic metabolite of acetaminophen.
In this work, a novel DOPO-based epoxy curing agent via imine linkage was successfully synthesized by two-pot procedure.
Aziridine 2-methyl- is an imine which is widely spread in ten sampling stations out of thirteen (Table 7).
The implementation includes the solution's advanced iMine feature set, which automates the process of searching enterprise spend data for savings opportunity and other business performance improvement opportunities.
The method is comprised of attaching a reactive group X--Y to a surface of a pigment; and subsequently displacing Y with an organic substrate N--S--ZM to form a surface-modified pigment having attached X--N--S--ZM; wherein X is a sulfonyl, phosphoryl, or 1,3,5-triazine group; Y is fluorine, chlorine, bromine or iodine; N is an amine, an imine, a pyridine, or a thiol group; S is substituted or unsubstituted alkyls, aryls, or polymer chains having a molecular weight range from approximately 300-8000; Z is a carboxyl, sulfonyl, phenolic, phosphoryl, ammonium, trimethylammonium, or tri-butylammonium group; and M is a halide, a negatively charged ion, a proton n salt form, or a cation in salt form.
Polyethylene imine (PEI) and saline were taken as positive and negative controls respectively for all studies.
Owe nowe imine wituwi ta diitake menta'yowi kaaramoniyu isa peenu
Candidate polyelectrolytes include polyacrylic acid, poly(acrylamide acrylic acid), poly(acryl amide-co-acrylic acid), sodium polystyrene sulfonate, polyethylene imine, polypeptides, and copolymers.
granting the Defendants' motion in I imine, to exclude Dr.
Volume 2 contains chapters on transition metal-catalyzed desulfitative coupling of thioorganic compounds with boronic acids; catalytic additions of allyllic boronates to carbonyl and imine derivatives; nucleophilic addition reactions to organoboronic acids; asymmetric homologation of boronic esters with lithiated carbamates, epoxides, and azirdines; borate and boronic acid derivatives as catalysts in organic synthesis.
Only a small amount (5%) is metabolized via the cytochrome P450 enzyme system to the alkylating metabolite N-acetyl-p- benzoquinone imine (NAPQI) which is responsible for the toxic effect (8).
For example, by aldehyde linking a hydrazone is formed from a hydrazine group [13], which is hydrolytically more stable than imine obtained from an amino group.