Devise a synthesis of the tripeptide sequence Phe Thr Lys using acid chloride below and N-methylmorpholine (NMM) for your coupling. Propose a detailed reaction mechanism for this step. You may use any readily available reagents/ protecting groups for your synthesis. In your answer you should clearly state the chosen reagents and how they are introduced and removed in your synthesis. Mechanistic details, for these steps are NOT required. Ph `NH2 NH NH3 `NH CO2 но Phe Thr Lys

give the retrosynthetic analysis which has an aromatic starting compound that gives this product and then the forward reaction stating all the reagents

Given the target molecule and it's synthons, propose it's synthetic equivalents and a forward synthesis.

Show the retrosynthetic analysis and foreward reaction of the following compounds. Please draw out the structures too.

Make an electron-flow-mechanism for this synthetic scheme. This involves predicting major and by-products using electronic and structural effects. The arrow push mechanism must be shows. (BENZENE -> 2-ACETOXYBENZOIC ACID or ASPIRIN)

By using only amide/Peptide bond forming rxn and a lkylation rxns. Provide all the reaction steps with the reagent needed and conditions with out showing the mechanism for each step to form the product. Note: Use protecting groups like (Boc, Fmoc, and others) H¸NNH rxns. By using only amide / Peptide bond forming rxn and alkylation Provide all the reaction steps with the reagent needed and conditions showing the mechanism for each step to form the product. protecting groups. like (Boc, Fmoc, and others) with out Note: Use HN H₂N. -NH₂- + ΝΗ

Give a clear explanation handwritten answer..give the mechanism of given bleow reactions

The following reaction is an example of a "thiol/ene" Michael reaction. It's commonly used to modify polymers as shown below. Provide a mechanism. Triethylamine is used as a base.

افي can you create an original syntheic scheme to the given target and write a paragraph that descibe the reagents/solvents being used and the name of the mechanism/reaction perfomed (should be like a scientific journal article) C ง