Chapter 29: Q65. (page 1197)
Draw the mechanism for the reaction that removes an Fmoc group from an amino acid under the following conditions:
Chapter 29: Q65. (page 1197)
Draw the mechanism for the reaction that removes an Fmoc group from an amino acid under the following conditions:
All the tools & learning materials you need for study success - in one app.
Get started for freeBesides the Boc and Fmoc protecting groups used in peptide synthesis, amines can also be protected by reaction with benzyl chloroformate. Draw the structure of the product formed by reaction of alanine with benzyl chloroformate.
Devise a synthesis of threonine from diethyl acetamidomalonate.
What steps are needed to convert A to L-dopa, an uncommon amino acid that is effective in treating Parkinsonโs disease? These steps are the key reactions in the first commercial asymmetric synthesis using a chiral transition metal catalyst. This process was developed at Monsanto in 1974.
Draw the organic products formed in each reaction.
a.
b.
Question:Draw the product formed when the following amino acid is treated with each reagent: (a) (b) , pyridine; (c) HCl (1 equiv); (d) NaOH (1 equiv); (e).
What do you think about this solution?
We value your feedback to improve our textbook solutions.