enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Carbenoid - Wikipedia

    en.wikipedia.org/wiki/Carbenoid

    In chemistry a carbenoid is a reactive intermediate that shares reaction characteristics with a carbene. [1] In the Simmons–Smith reaction the carbenoid intermediate is a zinc / iodine complex that takes the form of I-CH 2-Zn-I. This complex reacts with an alkene to form a cyclopropane just as a carbene would do.

  3. Simmons–Smith reaction - Wikipedia

    en.wikipedia.org/wiki/Simmons–Smith_reaction

    The Charette modification replaces the CH 2 I 2 normally found in the Simmons–Smith reaction with aryldiazo compounds, such as phenyldiazomethane, in Pathway A. [30] Upon treatment with stoichiometric amounts of zinc halide, an organozinc compound similar to the carbenoid discussed above is produced. This can react with almost all alkenes and ...

  4. Metal-catalyzed cyclopropanations - Wikipedia

    en.wikipedia.org/wiki/Metal-catalyzed_cyclopropa...

    The configuration of the product is determined by the trajectory of approach of the olefin to the metal carbene. In reactions of monosubstituted metal carbenes with terminal olefins, the olefin likely approaches "end-on" (with the carbon-carbon double bond of the olefin nearly parallel to the metal-carbon double bond of the carbene) with the olefin R group pointed away from the substituent of ...

  5. Transition metal carbene complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_carbene...

    A transition metal carbene complex is an organometallic compound featuring a divalent carbon ligand, itself also called a carbene. [1] Carbene complexes have been synthesized from most transition metals and f-block metals, [2] using many different synthetic routes such as nucleophilic addition and alpha-hydrogen abstraction. [1]

  6. Carbene - Wikipedia

    en.wikipedia.org/wiki/Carbene

    Carbene intramolecular reaction Carbene intermolecular reaction The 1,2-rearrangement produced from intramolecular insertion into a bond adjacent to the carbene center is a nuisance in some reaction schemes, as it consumes the carbene to yield the same effect as a traditional elimination reaction . [ 16 ]

  7. Fischer carbene - Wikipedia

    en.wikipedia.org/wiki/Fischer_carbene

    The strong electron withdrawing nature of Fischer carbenes is also reflected in many reactions. For instance, the Diels–Alder reaction between methyl acrylate and isoprene is completed in 7 days at room temperature with low para-meta selectivity. On the other hand, the Fischer carbene counterpart finished in 3 hours at room temperature with ...

  8. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    Often cross-coupling reactions require metal catalysts. One important reaction type is this: R−M + R'−X → R−R' + MX (R, R' = organic fragments, usually aryl; M = main group center such as Li or MgX; X = halide) These reactions are used to form carboncarbon bonds but also carbon-heteroatom bonds.

  9. Shi epoxidation - Wikipedia

    en.wikipedia.org/wiki/Shi_epoxidation

    Shi epoxidation with modern reaction conditions. The Shi epoxidation is a chemical reaction described as the asymmetric epoxidation of alkenes with oxone (potassium peroxymonosulfate) and a fructose-derived catalyst (1). This reaction is thought to proceed via a dioxirane intermediate, generated from the catalyst ketone by oxone (potassium ...