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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. 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.

  5. 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'.

  6. Atom transfer radical polymerization - Wikipedia

    en.wikipedia.org/wiki/Atom_Transfer_Radical...

    The transition metal catalyst should not lead to significant side reactions, such as irreversible coupling with the propagating radicals and catalytic radical termination; The most studied catalysts are those that include copper, which has shown the most versatility with successful polymerizations for a wide selection of monomers.

  7. 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 ...

  8. Ullmann condensation - Wikipedia

    en.wikipedia.org/wiki/Ullmann_condensation

    Illustrative of the traditional Ullmann ether synthesis is the preparation of p-nitrophenyl phenyl ether from 4-chloronitrobenzene and phenol. [2] O 2 NC 6 H 4 Cl + C 6 H 5 OH + KOH → O 2 NC 6 H 4 O−C 6 H 5 + KCl + H 2 O. Copper is used as a catalyst, either in the form of the metal or copper salts. Modern arylations use soluble copper ...

  9. Iron - Wikipedia

    en.wikipedia.org/wiki/Iron

    Iron-carbon phase diagram. α-Iron is a fairly soft metal that can dissolve only a small concentration of carbon (no more than 0.021% by mass at 910 °C). [133] Austenite (γ-iron) is similarly soft and metallic but can dissolve considerably more carbon (as much as 2.04% by mass at 1146 °C).