Talk:Alpha, beta unsaturated ketone: Difference between revisions
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This mechanism forms an enol, which then attacks the carbonyl of another molecule. The molecule then undergoes E1cb to eliminate the hydroxy group and form a carbon-carbon double bond. | This mechanism forms an enol, which then attacks the carbonyl of another molecule. The molecule then undergoes E1cb to eliminate the hydroxy group and form a carbon-carbon double bond. | ||
[[File:Alpha-Beta_Unsaturated_Ketone_Formation.png|550px]] | [[File:Alpha-Beta_Unsaturated_Ketone_Formation.png|550px]] | ||
== Robinson Annulation, Samuel Alves-Czachor == | |||
[[File: Wiki 4 samuel alves-czachor.png|1100px]] | |||
Revision as of 21:07, 5 May 2019
Condensation of Ketone to Alpha, Beta Unsaturated Carbonyl
This mechanism forms an enol, which then attacks the carbonyl of another molecule. The molecule then undergoes E1cb to eliminate the hydroxy group and form a carbon-carbon double bond.
Robinson Annulation, Samuel Alves-Czachor
