Answer:

4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required...
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. HH iPr Meo, co Me co, 8. 2. 3. 7. 5. Me NH2 Me MeOCCO Me 6.
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Η. Η Me MeOCCO,Me 1. 8. 2. 9 3 7. 4. 5 NH2 6 MeOCCO Me
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me NH но HK он 1 4 5. 6. 3. 2. NH2 O) 08
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me NH но HK он 1 4 5....
4.(3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. ~ Me но ме -O Me
4.(3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me HO Me го ме
Using retrosynthetic analysis,
provide a synthesis for the following molecule. Place the required
reagents next to the arrows and the necessary
HH iPr: + MeOCCO Me 1. 8. 2. 9. 3. 7. 4. 5. Me NH2 6. Me MeOCCO Me
provide a synthesis for the following molecule. Place the required the necessary intermediates in the boxes provided. 4. (12 pts) Using retrosynthetic analysis, a reagents next to the arrows and necessary Me t-Bu MgBr
provide a synthesis for the following molecule. Place the required the necessary intermediates in the boxes provided. 4. (12 pts) Using retrosynthetic analysis, a reagents next to the arrows and necessary Me t-Bu MgBr
Propose a synthesis using the target molecule with
retrosynthetic analysis.
Provide complete reagents for each step of your proposed
synthesis.
from Target molecule
from Target molecule
1. Perform a retrosynthetic analysis on the following molecule from the given starting materials (13 pts). Me Me Ph 1. 9 2. 10. 3. 6. 4. 7. 5.
7. For the compound below provide a stepwise retrosynthetic analysis and a separate forward synthesis showing reagents and solvents used. Make sure you justify the regio- selectivity. (12 pts.) and any reagents of 2 carbons or less.