Question 6.(continued) Subsequent steps in this synthesis of morphine are illustrated in the following scheme. (b)...
Question 6.(continued) Subsequent steps in this synthesis of morphine are illustrated in the following scheme. (b) MeO Meo NHMe но COOMeO, он MeO OMe но. Meo NMe NMe но Codeine Morphine Propose a synthetic route to compound F including all reagents and isolated intermediates. Hint: the methyl ester should be made from the corresponding acid using mild conditions. (0) from compound E (several steps), 17) Write the retrosynthesis of codeine leading back to compound G, clearly indicating the disconnections and the starting materials (you do not need to show the corresponding synthons), and describing the transformations corresponding to the forward direction. (ii) 15)