has an OH group attached to one end of the double bond. It is called an enolate if the proton on the oxygen atom is taken away. Enols are tautomers of...

chemistry. It is a chemical reaction between an enolate ion and a conjugated carbonyl compound. The enolate ion acts as a nucleophile and is called the Michael...

hydrogen atom from the activated methylene bridge to make an enolate reaction intermediate. The enolate is a nucleophile that attacks one end of the dibromide...

becomes delocalised across the oxygen atom and the α carbon, making an enolate. Protonation happens at the α carbon, so the product keeps the carbonyl...

reaction with ethyl acetate and an alkoxide base like sodium ethoxide via an enolate intermediate. Cortney, Candice H.; Krishnan, V. V. (2020). "Keto–Enol Tautomerization...

to make many organolithium compounds, including acetylides or lithium enolates. Amonoo-Neizer, E. H.; Shaw, R. A.; Skovlin, D. O.; Smith, B. C.; Rosenthal...

it uses a basic catalyst, changing the isocyanide's carbonyl into an enolate that acts as a Michael donor. Blicke, F. F.; Powers, J. L. (1927). "Preparation...