Propose a synthesis using the target molecule with retrosynthetic analysis.
Provide complete reagents for each step of your proposed synthesis.
. . . If you have any doubt in any step, please let me know. Thank you.
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
using any reagents show retrosynthetic analysis and then show entire synthesis in forward sense SIcP f youl proposed syninesis. from Target molecule SIcP f youl proposed syninesis. from Target molecule
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
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....
What is the Retrosynthetic Analysis and Proposed Synthesis? blo-olie any inorganic reagents
1. Provide a complete retrosynthesis and forward synthesis of the target molecule below from the given starting materials. All carbons of the target must be from the given starting materials. You may use any reagents you find necessary. You may include more than one step over a reaction arrow, but please no more than 3 steps at a time. Please show the key intermediates in your synthesis for partial credit. (10 bonus points) For full credit, include a retrosynthetic analysis,...
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. Η Η N iPr MeO2C CO Me co 1. 8. 2. 9. 3. 7. 4. 5. Me NH2 6. Me MeOCCO Me