1) When synthesising potential peptide drugs, it is often necessary to use unnatural amino acids. It is essential that we know the stereochemistry of these unnatural amino acids. Below are two line structures of two unnatural amino acids. Draw the S--enantiomer of each of these structures. + H₂N COO CH₂Br مشرق N.

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter27: Amino Acids And Proteins
Section: Chapter Questions
Problem 27.39P: A chemically modified guanidino group is present in cimetidine (Tagamet), a widely prescribed drug...
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1) When synthesising potential peptide drugs, it is often necessary to use unnatural
amino acids. It is essential that we know the stereochemistry of these unnatural
amino acids. Below are two line structures of two unnatural amino acids. Draw the
S--enantiomer of each of these structures.
+
H₂N
COO
CH₂Br
مشرق
N.
Transcribed Image Text:1) When synthesising potential peptide drugs, it is often necessary to use unnatural amino acids. It is essential that we know the stereochemistry of these unnatural amino acids. Below are two line structures of two unnatural amino acids. Draw the S--enantiomer of each of these structures. + H₂N COO CH₂Br مشرق N.
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