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Others, however, insist that such a usage is an abuse of terminology, and limit the Michael addition to the formation of carbon–carbon bonds through the addition of carbon nucleophiles. The terms oxa-Michael reaction and aza-Michael reaction [2] have been used to refer to the 1,4-addition of oxygen and nitrogen nucleophiles, respectively. The ...
The Stork enamine alkylation involves the addition of an enamine to a Michael acceptor (e.g., an α,β -unsaturated carbonyl compound) or another electrophilic alkylation reagent to give an alkylated iminium product, which is hydrolyzed by dilute aqueous acid to give the alkylated ketone or aldehyde. [1]
Robinson annulation is one notable example of a wider class of chemical transformations termed Tandem Michael-aldol reactions, that sequentially combine Michael addition and aldol reaction into a single reaction. As is the case with Robinson annulation, Michael addition usually happens first to tether the two reactants together, then aldol ...
One of the most common variations of the Nenitzescu reaction is the solid phase variant. This reaction, first reported by Ketcha et al., is shown below. [3] Description of the solid-phase Nenitzescu indole synthesis. It takes place on a highly cross-linked ArgoPore®-Rink-NH-Fmoc resin and functions with a variety of substituents on both ...
Nef reaction in combination with Michael addition. In carbohydrate chemistry, they are a chain-extension method for aldoses, as in the isotope labeling of C 14-D‑mannose and C 14-D‑glucose from D‑arabinose and C 14 ‑nitromethane (the first step here is a Henry reaction): The Nef reaction: chain extension. The opposite reaction is the ...
The vinylsulfone group reacts with the nucleophilic functional groups of the fibers by Michael addition to form a covalent ether bond: Reaction of vinyl sulfone compounds with hydroxyl groups of cellulose (HO-CELL) An unfavorable side reaction in the dyeing process is the conversion of the vinylsulfone group to the 2-(hydroxy)ethylsulfonyl ...
An addition reaction is the reverse of an elimination reaction, in which one molecule divides into two or more molecules. For instance, the hydration of an alkene to an alcohol is reversed by dehydration. There are two main types of polar addition reactions: electrophilic addition and nucleophilic addition.
Arthur Michael is remembered today primarily for the Michael reaction, also called the Michael addition. As originally defined by Michael, the reaction involves the combination of an enolate ion of a ketone or aldehyde to an α,β-unsaturated carbonyl compound at the β carbon. [6] Michael was also well known in his day for incorporating ...