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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. [1] [2] [3]
Cross-couplings are a subset of the more general coupling reactions. 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 carbon–carbon bonds but ...
Examples of gluon coupling. Particles which interact with each other are said to be coupled. This interaction is caused by one of the fundamental forces, whose strengths are usually given by a dimensionless coupling constant. In quantum electrodynamics, this value is known as the fine-structure constant α, approximately equal to 1/137.
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.
In organic chemistry, an azo coupling is an reaction between a diazonium compound (R−N≡N +) and another aromatic compound that produces an azo compound (R−N=N−R’).In this electrophilic aromatic substitution reaction, the aryldiazonium cation is the electrophile, and the activated carbon (usually from an arene, which is called coupling agent), serves as a nucleophile.
Pages in category "Coupling reactions" The following 83 pages are in this category, out of 83 total. This list may not reflect recent changes. ...
The McMurry reaction of benzophenone. The McMurry reaction is an organic reaction in which two ketone or aldehyde groups are coupled to form an alkene using a titanium chloride compound such as titanium(III) chloride and a reducing agent. The reaction is named after its co-discoverer, John E. McMurry.
The reaction was described in 1963 by chemists Castro and Stephens. [ 1 ] [ 2 ] The reaction is similar to the much older Rosenmund–von Braun synthesis (1914) [ 3 ] [ 4 ] between aryl halides and copper(I) cyanide and was itself modified in 1975 as the Sonogashira coupling by adding a palladium catalyst and preparing the organocopper compound ...