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  2. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    Many mechanisms exist reflecting the myriad types of cross-couplings, including those that do not require metal catalysts. [7] Often, however, cross-coupling refers to a metal-catalyzed reaction of a nucleophilic partner with an electrophilic partner. Mechanism proposed for Kumada coupling (L = Ligand, Ar = Aryl).

  3. 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 ]

  4. Dialkylbiaryl phosphine ligands - Wikipedia

    en.wikipedia.org/wiki/Dialkylbiaryl_phosphine...

    Many Pd-catalyzed cross coupling reactions involve oxidative addition to form Pd(II) derivatives called oxidative addition complexes (OAC). The resulting L–Pd II (Ar)X OAC is electrophilic such that it reacts with a nucleophile and forms CC and C–heteroatom bonds, after reductive elimination. [61] Such Pd II OACs have been used as ...

  5. 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:

  6. Ullmann condensation - Wikipedia

    en.wikipedia.org/wiki/Ullmann_condensation

    The coupling of 2-chlorobenzoic acid and aniline is illustrative: [4] C 6 H 5 NH 2 + ClC 6 H 4 CO 2 H + KOH → C 6 H 5 N(H)−C 6 H 4 CO 2 H + KCl + H 2 O. A typical catalyst is formed from copper(I) iodide and phenanthroline. The reaction is an alternative to the Buchwald–Hartwig amination reaction.

  7. Heterogeneous metal catalyzed cross-coupling - Wikipedia

    en.wikipedia.org/wiki/Heterogeneous_metal...

    Pd/C catalyzed cross coupling performed on 2.5 kg scale in 85% yield with <10 ppm residual Pd following filtration and DMF washing. When designing a polymer-ligand solid support for Pd, the ligands should not simply be immobilized variants of homogeneous ligands which effect catalysis in the presence of Pd.

  8. Decarboxylative cross-coupling - Wikipedia

    en.wikipedia.org/wiki/Decarboxylative_cross-coupling

    The most typical class of reactions involves coupling between C–COOH and C–X bonds, however C–COOH and C–M cross-coupling, homo-coupling of carboxylic acids, heck coupling, and dehydrogenative cross-coupling can also be including in this class as they release CO 2. Heteroatom cross coupling reactions involving formation of C–N, C–S ...

  9. 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 ...