Chapter 29: Q5. (page 1157)
What - halo carbonyl compoundis needed to synthesize each amino acid?
(a) Glycine
(b) Isoleucine
(c) Phenylalanine
Short Answer
(a)
(b)
(c)
Chapter 29: Q5. (page 1157)
What - halo carbonyl compoundis needed to synthesize each amino acid?
(a) Glycine
(b) Isoleucine
(c) Phenylalanine
(a)
(b)
(c)
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Get started for freeQuestion: Identify the nucleophile and the electrophile in the following acid–base reactions:
How many different tripeptides can be formed from three different amino acids?
Draw the organic products formed in each reaction.
Give the amino acid sequence of an octapeptide that contains the amino acids Tyr, Ala, Leu (2 equiv), Cys, Gly, Glu and Val, and forms the following fragments when partially hydrolyzed with HCl: Val-Cys-Gly-Glu, Ala-Leu-Tyr, and Tyr-Leu-Val-Cys.
What steps are needed to convert A to L-dopa, an uncommon amino acid that is effective in treating Parkinson’s 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.
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