The Robinson annulation is a combination of two carbonyl coupling reactions, the Michael reaction and the intramolecular aldol condensation. The most common partners in the reaction are a nucleophilic donor (such as a cyclic ketone, a B-keto ester, an enamine, or a B-diketone) and an a6-unsaturated ketone acceptor. The product is a substituted 2-cyclohexenone derivative. Draw the structures of the nucleophilic B-diketone and the aB-unsaturated ketone acceptor that were combined in a Robinson annulation to give the following product: Ph opy ato

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The Robinson annulation is a combination of two carbonyl coupling reactions, the Michael reaction and the intramolecular aldol condensation. The most common partners in the reaction are a
nucleophilic donor (such as a cyclic ketone, a ß-keto ester, an enamine, or a 6-diketone) and an a 6-unsaturated ketone acceptor The product is a substituted 2-cyclohexenone derivative.
Draw the structures of the nucleophilic B-diketone and the a B-unsaturated ketone acceptor that wvere combined in a Robinson annulation to give the following product:
Ph
C P
000- IF
Transcribed Image Text:The Robinson annulation is a combination of two carbonyl coupling reactions, the Michael reaction and the intramolecular aldol condensation. The most common partners in the reaction are a nucleophilic donor (such as a cyclic ketone, a ß-keto ester, an enamine, or a 6-diketone) and an a 6-unsaturated ketone acceptor The product is a substituted 2-cyclohexenone derivative. Draw the structures of the nucleophilic B-diketone and the a B-unsaturated ketone acceptor that wvere combined in a Robinson annulation to give the following product: Ph C P 000- IF
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