In organic chemistry, enolates are organic anions derived from the deprotonation of carbonyl (RR'C=O) compounds. Rarely isolated, they are widely used as reagents in the synthesis of …

Aug 16, 2022 · Enolates can be formed through removing the proton on carbons adjacent to a carbonyl (i.e. the “ alpha-carbon “). The resulting anions are much more stable than typical …

The last major class of reactions involves C-C bond formation that proceeds through an intermediate known as an enolate. An enolate is simply a deprotonated enol, which is itself a …

Apr 16, 2025 · Enolates are reactive intermediates in organic chemistry that play a central role in forming carbon–carbon bonds. They are formed by deprotonating the α-hydrogen of carbonyl …

What is Enolate? Enolates, also known as oxyallyl anions, are flexible reagents that may be used to make -substituted carbonyl compounds, making them crucial intermediates in the synthesis …

An enolate is the conjugate base of an enol, typically generated by deprotonating the α-carbon (carbon adjacent to the carbonyl) of aldehydes or ketones. Enolates are highly nucleophilic …

Jun 9, 2025 · Enolate formation is the initial step in a series of reactions that are pivotal in organic synthesis. An enolate is a resonance-stabilized anion formed by the removal of a proton from …

Ketones and aldehydes are two very important types of organic compounds. This article will focus on enols and enolates, which are two closely related forms that give ketones and aldehydes …

Since the negative charge of an enolate anion is delocalized over the alpha-carbon and the oxygen, as shown earlier, electrophiles may bond to either atom. Reactants having two or …

Aug 19, 2022 · This review covers various methods for enolate formation, and has data on the composition of various ketone-enolate mixtures formed under kinetic and thermodynamic …