The Robinson carbonyl coupling reactions, the Michael reaction and the intramolecular aldol condensation. The most common partners in the li donor (such as a cyclic ketone, a β-keto ester, an enamine, or a β-diketone) and an α,β-unsaturated ketone acceptor. The product is a substituted 2-cyclohexenone derivative annulation is a combination of two reaction are a nucleophi Draw the structures of the nucleophilic B-keto ester and the α,β-unsaturated ketone acceptor that were combined in a Robinson annulation to give the following product Ph Ph Ph Ph CO2Et Draw the B-keto ester as an ethyl ester
The Robinson carbonyl coupling reactions, the Michael reaction and the intramolecular aldol condensation. The most common partners in the li donor (such as a cyclic ketone, a β-keto ester, an enamine, or a β-diketone) and an α,β-unsaturated ketone acceptor. The product is a substituted 2-cyclohexenone derivative annulation is a combination of two reaction are a nucleophi Draw the structures of the nucleophilic B-keto ester and the α,β-unsaturated ketone acceptor that were combined in a Robinson annulation to give the following product Ph Ph Ph Ph CO2Et Draw the B-keto ester as an ethyl ester
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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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
Draw the structures of the nucleophilic β-keto ester and the α,β-unsaturated ketone acceptor that were combined in a Robinson annulation to give the following product:
- Draw the β-keto ester as an ethyl ester,
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