Abstract:A Michael-aldol domino reaction sequence of acenaphthenequinone with acetophenone in the presence of KOH in methanol solvent leading to the formation of three different 2:2 adducts arising through three distinct reaction sequences is described. Similar sequences leading to a highly substituted furan derivative were observed in the reaction between phenanthrenequinone and acetophenone.
Metal and acid-free synthesis of acenaphthenone-2-ylidene ketones in PEG 400 has been developed. Using TBN, a radical nitration of acenaphthenone-2-ylidene ketones has been accomplished for the first time.
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