Could someone help me draw out the mechanism for this reaction? This was the description of the steps...
Step 1) Ring opening of aziridine + MeOH addition
Step 2) Acetylative debenzylation with Pd(OH)2 and acetic anhydride
Step 3) Treatment with benzylamine in presence of Me3Al
Could someone help me draw out the mechanism for this reaction? This was the description of...
Using the list, propose the forward synthesis of the retrosynthesis shown below (any number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially. Оме Meo Оме Meo Meo A. Ph3PMeBr, KotBu, PhMe, 25 °C B. CuBr, 0 °C C. Cu20, Cu(NO3)2, H20, 0 °C D. CuCN, 0 °C E. SO3, H2SO4, 100 °C F. Cl2, FeCl3, THF, 65 °C...