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. Η Η N iPr MeO2C CO Me co 1. 8. 2. 9. 3. 7. 4. 5. Me NH2 6. Me 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. Η. Η Me MeOCCO,Me 1. 8. 2. 9 3 7. 4. 5 NH2 6 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
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
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
9) (marks = 3) Provide a reasonable multistep synthesis of the following molecule from the indicated starting material, using any reagents necessary. Please include both a retrosynthesis and a forward synthesis (that includes the product and reagents of each individual step in your synthesis). Meo. = Me Me as a racemic mixture These reagents are your only sources of carbon and both are to be used at different steps of your synthesis
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