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  2. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carboncarbon_bond

    The carboncarbon single bond is a sigma bond and is formed between one hybridized orbital from each of the carbon atoms. In ethane, the orbitals are sp 3-hybridized orbitals, but single bonds formed between carbon atoms with other hybridizations do occur (e.g. sp 2 to sp 2). In fact, the carbon atoms in the single bond need not be of the ...

  3. Category:Carbon-carbon bond forming reactions - Wikipedia

    en.wikipedia.org/wiki/Category:Carbon-carbon...

    This is a category devoted to reactions which form carbon-carbon bonds (single, double and triple). Please note that a related category devoted to reactions which form carbon-heteroatom bonds exists at Category:Carbon-heteroatom bond forming reactions

  4. 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 ]

  5. Michael addition reaction - Wikipedia

    en.wikipedia.org/wiki/Michael_Addition_Reaction

    Some authors have broadened the definition of the Michael addition to essentially refer to any 1,4-addition reaction of α,β-unsaturated carbonyl compounds. Others, however, insist that such a usage is an abuse of terminology, and limit the Michael addition to the formation of carboncarbon bonds through the addition of carbon nucleophiles.

  6. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    Frequently, however, C–Cl bonds are too inert, and bromide or iodide leaving groups are required for acceptable rates. The main group metal in the organometallic partner usually is an electropositive element such as tin , zinc , silicon, or boron .

  7. Henry reaction - Wikipedia

    en.wikipedia.org/wiki/Henry_reaction

    The Henry reaction is a classic carbon–carbon bond formation reaction in organic chemistry.Discovered in 1895 by the Belgian chemist Louis Henry (1834–1913), it is the combination of a nitroalkane and an aldehyde or ketone in the presence of a base to form β-nitro alcohols.

  8. Sonogashira coupling - Wikipedia

    en.wikipedia.org/wiki/Sonogashira_coupling

    The Sonogashira cross-coupling reaction has been employed in a wide variety of areas, due to its usefulness in the formation of carboncarbon bonds. The reaction can be carried out under mild conditions, such as at room temperature, in aqueous media, and with a mild base, which has allowed for the use of the Sonogashira cross-coupling ...

  9. Coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Coupling_reaction

    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'. The most common type of coupling reaction is the cross coupling reaction.