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  2. Amine - Wikipedia

    en.wikipedia.org/wiki/Amine

    Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group [4] (these may respectively be called alkylamines ...

  3. Aliphatic amine - Wikipedia

    en.wikipedia.org/?title=Aliphatic_amine&redirect=no

    From a subtopic: This is a redirect from a subtopic of the target article or section.. If the redirected subtopic could potentially have its own article in the future, then also tag the redirect with {{R with possibilities}} and {{R printworthy}}.

  4. Béchamp reduction - Wikipedia

    en.wikipedia.org/wiki/Béchamp_reduction

    Tertiary aliphatic nitro compounds, however, are converted in good yield to the amine using the Béchamp reduction. [6] The reduction proceeds in a multistep manner. First, the nitro group is reduced to nitroso, which undergoes hydrogenation to a hydroxylamino group prior to further reduction to the amine. [7] Proposed mechanism of the Bechamp ...

  5. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Aliphatic compounds can be saturated, joined by single bonds (), or unsaturated, with double bonds or triple bonds ().If other elements (heteroatoms) are bound to the carbon chain, the most common being oxygen, nitrogen, sulfur, and chlorine, it is no longer a hydrocarbon, and therefore no longer an aliphatic compound.

  6. Zincke reaction - Wikipedia

    en.wikipedia.org/wiki/Zincke_reaction

    With secondary amines and not primary amines the Zincke reaction takes on a different shape forming so-called Zincke aldehydes in which the pyridine ring is ring-opened with the terminal iminium group hydrolyzed to an aldehyde: [4] Zincke aldehydes. This variation has been applied in the synthesis of novel indoles: [11] Zincke aldehydes Kearney ...

  7. Borylation - Wikipedia

    en.wikipedia.org/wiki/Borylation

    Borylation occurs selectively at the least sterically hindered and least electron rich primary C–H bond in a range of acetals, ethers, amines, and alkyl fluorides. [10] Additionally, no reaction is shown to occur in the absence of primary C–H bonds, for example when cyclohexane is the substrate. Aliphatic C–H borylation

  8. Alkylamines - Wikipedia

    en.wikipedia.org/wiki/Alkylamines

    Aliphatic amine; Psychotropic alkylamines This page was last edited on 27 December 2020, at 15:36 (UTC). Text is available under the Creative Commons ...

  9. Epoxy - Wikipedia

    en.wikipedia.org/wiki/Epoxy

    Aliphatic, cycloaliphatic and aromatic amines are all employed as epoxy hardeners. Amine type hardeners will alter both the processing properties (viscosity, reactivity) and the final properties (mechanical, temperature and heat resistance) of the cured copolymer network. Thus amine structure is normally selected according to the application.