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  2. Nierenstein reaction - Wikipedia

    en.wikipedia.org/wiki/Nierenstein_reaction

    The unreactive diazoketone can be re-activated and reacted by treatment with hydrogen chloride to give the normal Nierenstein product. The Nierenstein reaction mechanism. In some cases, even limiting the amount of diazomethane gives a reaction process that stalls via the neutral diazoketone pathway, requiring the addition of HCl gas to rescue ...

  3. Carbon–hydrogen bond activation - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond...

    The selective activation and functionalization of alkane C–H bonds was reported using a tungsten complex outfitted with pentamethylcyclopentadienyl, nitrosyl, allyl and neopentyl ligands, Cp*W(NO)(η 3-allyl)(CH 2 CMe 3). [11] C–H activation of pentane, as seen in Ledgzdins et al., J. Am. Chem. Soc. 2007; 129, 5372–3.

  4. Oxygen rebound mechanism - Wikipedia

    en.wikipedia.org/wiki/Oxygen_rebound_mechanism

    Dissociation of the alcohol from the metal allows the cycle to start anew. This mechanistic scenario is an alternative to the direct insertion of an O center into a C-H bond. The pathway is an example of C-H activation. [1] [2] Steps in an oxygen rebound mechanism: H-atom abstraction, oxygen rebound, alcohol decomplexation.

  5. Büchner–Curtius–Schlotterbeck reaction - Wikipedia

    en.wikipedia.org/wiki/Büchner–Curtius...

    Mechanisms for formations of the carbonyl products. The epoxide product is formed by an intramolecular addition reaction in which a lone pair from the oxygen attacks the carbocation (6). Mechanism for the formation of the epoxide product. This reaction is exothermic due to the stability of nitrogen gas and the carbonyl containing compounds.

  6. CH2N2 - Wikipedia

    en.wikipedia.org/wiki/CH2N2

    CH 2 N 2 may refer to: . Cyanamide, an organic compound; Diazirine, class of organic molecules with a cyclopropene-like ring, 3H-diazirene; Diazomethane, chemical compound discovered in 1894

  7. Carbon-carbon bond activation - Wikipedia

    en.wikipedia.org/wiki/Carbon-carbon_bond_activation

    Carbon-carbon bond activation refers to the breaking of carbon-carbon bonds in organic molecules. This process is an important tool in organic synthesis , as it allows for the formation of new carbon-carbon bonds and the construction of complex organic molecules. [ 1 ]

  8. Carbon cycle - Wikipedia

    en.wikipedia.org/wiki/Carbon_cycle

    Ocean mixed layer carbon, c m, is the only explicitly modelled ocean stock of carbon; though to estimate carbon cycle feedbacks the total ocean carbon is also calculated. [ 107 ] Current trends in climate change lead to higher ocean temperatures and acidity , thus modifying marine ecosystems. [ 108 ]

  9. Shilov system - Wikipedia

    en.wikipedia.org/wiki/Shilov_system

    Shilov cycle The overall charge is omitted from the complexes since the exact coordination sphere of the active species is unknown. The Shilov system is a classic example of catalytic C-H bond activation and oxidation which preferentially activates stronger C-H bonds over weaker C-H bonds for an overall partial oxidation.