Design a three-step synthesis for the following conversion using a Diels-Alder cycloaddition reaction. Disregard stereochemistry and competing products. 0¬AC -d Part: 0/4 Part 1 of 4 CN CH3 Draw the retrosynthetic dienophile precursor to the target molecule. Disregard stereochemistry and competing products. CN 4-¯ CH₂ 1 Sm mi

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Chapter1: Chemical Foundations
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Design a three-step synthesis for the following conversion using a Diels-Alder cycloaddition reaction. Disregard stereochemistry and competing products.
s-dr
Part: 0/4
Part 1 of 4
CN
CN
A-
CH3
CH₂
Draw the retrosynthetic dienophile precursor to the target molecule. Disregard stereochemistry and competing products.
B
+
Transcribed Image Text:Design a three-step synthesis for the following conversion using a Diels-Alder cycloaddition reaction. Disregard stereochemistry and competing products. s-dr Part: 0/4 Part 1 of 4 CN CN A- CH3 CH₂ Draw the retrosynthetic dienophile precursor to the target molecule. Disregard stereochemistry and competing products. B +
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