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Fukuyama coupling is a palladium-catalyzed reaction involving the coupling of an aryl, alkyl, allyl, or α,β- unsaturated thioester compound. This thioester compound can be coupled to a wide range of organozinc reagents in order to reveal the corresponding ketone product.
Logical coupling (or evolutionary coupling or change coupling) analysis exploits the release history of a software system to find change patterns among modules or classes: e.g., entities that are likely to be changed together or sequences of changes (a change in a class A is always followed by a change in a class B).
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The Correlation Spectroscopy experiment operates by correlating nuclei coupled to each other through scalar coupling, also known as J-coupling. [8] This coupling is the interaction between nuclear spins connected by bonds, typically observed between nuclei that are 2-3 bonds apart (e.g., vicinal protons).
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A typical example of classic Ullmann biaryl coupling is the conversion of ortho-chloronitrobenzene into 2,2'-dinitrobiphenyl with a copper - bronze alloy. [9] [10] 2 C 6 H 4 (NO 2)Cl + 2 Cu → (C 6 H 4 (NO 2)) 2 + 2 CuCl. The reaction has been applied to fairly elaborate substrates. Ullmann reaction
It can also be seen as the -OH's lone pairs pushing an alkyl group off as seen in the asymmetrical pinacol example. The migration of alkyl groups in this reaction occurs in accordance with their usual migratory aptitude , i.e. phenyl carbocation > hydride > tertiary carbocation (if formed by migration) > secondary carbocation (if formed by ...
A recent example in the area of chiral biaryl asymmetric catalysis employs a five-membered imidazole as part of the atropisomer scaffold. This specific phosphorus, nitrogen-ligand has been shown to perform enantioselective A 3 -coupling.