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  2. Carbon–nitrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbonnitrogen_bond

    A carbon–nitrogen bond is a covalent bond between carbon and nitrogen and is one of the most abundant bonds in organic chemistry and biochemistry. [1]Nitrogen has five valence electrons and in simple amines it is trivalent, with the two remaining electrons forming a lone pair.

  3. Imine - Wikipedia

    en.wikipedia.org/wiki/Imine

    In organic chemistry, an imine (/ ɪ ˈ m iː n / or / ˈ ɪ m ɪ n /) is a functional group or organic compound containing a carbon–nitrogen double bond (C=N). The nitrogen atom can be attached to a hydrogen or an organic group (R). The carbon atom has two additional single bonds.

  4. Double bond - Wikipedia

    en.wikipedia.org/wiki/Double_bond

    Double bonds are common for period 2 elements carbon, nitrogen, and oxygen, and less common with elements of higher periods. Metals, too, can engage in multiple bonding in a metal ligand multiple bond .

  5. Electrophilic amination - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_amination

    A nitrogen bound to both a good electrofuge and a good nucleofuge is known as a nitrenoid (for its resemblance to a nitrene). [2] Nitrenes lack a full octet of electrons are thus highly electrophilic; nitrenoids exhibit analogous behavior and are often good substrates for electrophilic amination reactions.

  6. Carbon compounds - Wikipedia

    en.wikipedia.org/wiki/Carbon_compounds

    In general bonds of carbon with other elements are covalent bonds. Carbon is tetravalent but carbon free radicals and carbenes occur as short-lived intermediates. Ions of carbon are carbocations and carbanions are also short-lived. An important carbon property is catenation as the ability to form long carbon chains and rings. [3]

  7. Buchwald–Hartwig amination - Wikipedia

    en.wikipedia.org/wiki/Buchwald–Hartwig_amination

    In organic chemistry, the Buchwald–Hartwig amination is a chemical reaction for the synthesis of carbon–nitrogen bonds via the palladium-catalyzed coupling reactions of amines with aryl halides. [1]

  8. Phenylalanine ammonia-lyase - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine_ammonia-lyase

    The enzyme is a member of the ammonia lyase family, which cleaves carbon–nitrogen bonds. Like other lyases, PAL requires only one substrate for the forward reaction, but two for the reverse. It is thought to be mechanistically similar to the related enzyme histidine ammonia-lyase (EC:4.3.1.3, HAL). [8]

  9. Hydrogenation of carbon–nitrogen double bonds - Wikipedia

    en.wikipedia.org/wiki/Hydrogenation_of_carbon...

    In chemistry, the hydrogenation of carbon–nitrogen double bonds is the addition of the elements of dihydrogen (H 2) across a carbon–nitrogen double bond, forming amines or amine derivatives. [1] Although a variety of general methods have been developed for the enantioselective hydrogenation of ketones, [ 2 ] methods for the hydrogenation of ...