4.(3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents...
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 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. 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. 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 N iPr MeO2C CO Me co 1. 8. 2. 9. 3. 7. 4. 5. Me NH2 6. Me MeOCCO Me
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
Provide retrosynthetic analysis and synthesize the following
molecule from acetylene and an alkyl halide.
3. Provide retrosynthetic analysis and synthesize the following molecule from acetylene and an alkyl halide: OH
8. 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. (10 pts) and any other reagents