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  2. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    In organic chemistry, a cross-coupling reaction is a reaction where two different fragments are joined. Cross-couplings are a subset of the more general coupling reactions. Often cross-coupling reactions require metal catalysts. One important reaction type is this:

  3. Coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Coupling_reaction

    The most common type of coupling reaction is the cross coupling reaction. [1] [2] [3] Richard F. Heck, Ei-ichi Negishi, and Akira Suzuki were awarded the 2010 Nobel Prize in Chemistry for developing palladium-catalyzed cross coupling reactions. [4] [5] Broadly speaking, two types of coupling reactions are recognized:

  4. Fermi contact interaction - Wikipedia

    en.wikipedia.org/wiki/Fermi_contact_interaction

    The interaction was first derived by Enrico Fermi in 1930. [7] A classical derivation of this term is contained in "Classical Electrodynamics" by J. D. Jackson. [8] In short, the classical energy may be written in terms of the energy of one magnetic dipole moment in the magnetic field B(r) of another dipole.

  5. Negishi coupling - Wikipedia

    en.wikipedia.org/wiki/Negishi_coupling

    The Negishi coupling is a widely employed transition metal catalyzed cross-coupling reaction. The reaction couples organic halides or triflates with organozinc compounds, forming carbon-carbon bonds (C-C) in the process. A palladium (0) species is generally utilized as the catalyst, though nickel is sometimes used.

  6. Hiyama coupling - Wikipedia

    en.wikipedia.org/wiki/Hiyama_coupling

    The Hiyama coupling is a palladium-catalyzed cross-coupling reaction of organosilanes with organic halides used in organic chemistry to form carbon–carbon bonds (C-C bonds). This reaction was discovered in 1988 by Tamejiro Hiyama and Yasuo Hatanaka as a method to form carbon-carbon bonds synthetically with chemo - and regioselectivity . [ 1 ]

  7. Transmetalation - Wikipedia

    en.wikipedia.org/wiki/Transmetalation

    Some of the cross-coupling reactions that include a transmetalation step are Stille cross-coupling, Suzuki cross-coupling, Sonogashira cross-coupling, and Negishi cross-coupling. The most useful cross-coupling catalysts tend to be ones that contain palladium. Cross-coupling reactions have the general form of R′–X + M–R → R′–R + M ...

  8. Coupling (physics) - Wikipedia

    en.wikipedia.org/wiki/Coupling_(physics)

    In physics, two objects are said to be coupled when they are interacting with each other. In classical mechanics, coupling is a connection between two oscillating systems, such as pendulums connected by a spring. The connection affects the oscillatory pattern of both objects.

  9. Oxidative coupling - Wikipedia

    en.wikipedia.org/wiki/Oxidative_coupling

    Oxidative coupling in chemistry is a coupling reaction of two molecular entities through an oxidative process.Usually oxidative couplings are catalysed by a transition metal complex like in classical cross-coupling reactions, although the underlying mechanism is different due to the oxidation process that requires an external (or internal) oxidant.