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  2. Organocopper chemistry - Wikipedia

    en.wikipedia.org/wiki/Organocopper_chemistry

    Organocopper chemistry is the study of the physical properties, reactions, and synthesis of organocopper compounds, which are organometallic compounds containing a carbon to copper chemical bond. [ 1 ] [ 2 ] [ 3 ] They are reagents in organic chemistry .

  3. Reactions of organocopper reagents - Wikipedia

    en.wikipedia.org/wiki/Reactions_of_organocopper...

    The addition of Grignard reagents to alkynes is facilitated by a catalytic amount of copper halide. Transmetalation to copper and carbocupration are followed by transmetalation of the product alkene back to magnesium. The addition is syn unless a coordinating group is nearby in the substrate, in which case the addition becomes anti and yields ...

  4. Stellar nucleosynthesis - Wikipedia

    en.wikipedia.org/wiki/Stellar_nucleosynthesis

    The proton–proton chain reaction starts at temperatures about 4 × 10 6 K, [30] making it the dominant fusion mechanism in smaller stars. A self-maintaining CNO chain requires a higher temperature of approximately 1.6 × 10 7 K, but thereafter it increases more rapidly in efficiency as the temperature rises, than does the proton–proton ...

  5. 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.

  6. Supernova nucleosynthesis - Wikipedia

    en.wikipedia.org/wiki/Supernova_nucleosynthesis

    Supernova nucleosynthesis is the nucleosynthesis of chemical elements in supernova explosions.. In sufficiently massive stars, the nucleosynthesis by fusion of lighter elements into heavier ones occurs during sequential hydrostatic burning processes called helium burning, carbon burning, oxygen burning, and silicon burning, in which the byproducts of one nuclear fuel become, after ...

  7. Coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Coupling_reaction

    Such reactions often require the aid of a metal catalyst. In one important reaction type, a main group organometallic compound of the type R-M (where R = organic group, M = main group centre metal atom) reacts with an organic halide of the type R'-X with formation of a new carbon-carbon bond in the product R-R'.

  8. 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 ]

  9. Ullmann reaction - Wikipedia

    en.wikipedia.org/wiki/Ullmann_reaction

    Aryl-Aryl bond formation is a fundamental tool in modern organic synthesis, with applications spanning natural product synthesis, pharmaceuticals, agrochemicals, and the development of commercial dyes and polyaromatics. With over a century of history, the Ullmann reaction has been one of the first to use a transition metal, primarily copper, in ...