2. Please provide a synthesis of the following molecule. (5 pts) OMe Meo
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,...
Ph y Ome 3. Synthesize the following acetal Me Retrosynthetic Analysis | Synthesis
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
Provide a step-wise synthesis of the molecule shown below using the two starting materials provided and anything else you may need. 5. Provide a stepwise synthesis of the molecule shown below using the two starting materials provided and anything else you may need. a. anything plus any other molecule containing 1 C plus any other reagents necessary. cl Hint: this is a highly convergent synthesis. You will need to prepare two separate molecules, then birng them together to form the...
5 Provide mechanism and product: I-BuOK PhCHO OH Me OMe Me 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 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....
a Provide synthesis of the molecule below from the required starting material OH Product Starting material
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