Chapter 29: Question 29.13 (page 1164)
What alkene is needed to synthesize each amino acid by an enantioselective hydrogenation reaction using and :
(a) Alanine;
(b) Leucine;
(c) Glutamine?
Short Answer
Answers
(a)
(b)
(c)
Chapter 29: Question 29.13 (page 1164)
What alkene is needed to synthesize each amino acid by an enantioselective hydrogenation reaction using and :
(a) Alanine;
(b) Leucine;
(c) Glutamine?
Answers
(a)
(b)
(c)
All the tools & learning materials you need for study success - in one app.
Get started for freeWhat alkyl halide is needed to synthesize each amino acid from diethyl acetamidomalonate: (a)Asn; (b)His; (c)Trp?
Draw the structure for each peptide:
(a) PheโAla;
(b) GlyโGln;
(c) LysโGly;
(d) R-H
The enolate derived from diethyl acetamidomalonate is treated with each of the following alkyl halides. After hydrolysis and decarboxylation, what amino acid is formed?
Draw the organic products formed in each reaction.
a.
b.
Another method to form a peptide bond involves a two-step process:
[1] Conversion of a Boc-protected amino acid to a p-nitrophenyl ester.
[2] Reaction of the p-nitrophenyl ester with an amino acid ester.
Why does a p-nitrophenyl ester โactivateโ the carboxy group of the first amino acid to amide formation?
Would a p-methoxyphenyl ester perform the same function? Why or why not?
What do you think about this solution?
We value your feedback to improve our textbook solutions.