1. Assuming you have available both enantiomers of the amino acid valine, how would you convert the iodide A shown below to the indicated carboxylic acid? You may assume other common reagents and solvents needed are also available. enantiosel. OBn alkylation OBn H₂N CO₂H (valine)

Organic Chemistry
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ISBN:9781305080485
Author:John E. McMurry
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Chapter20: Carboxylic Acids And Nitriles
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Problem 20VC: Electrostatic potential maps of anisole and thioanisole are shown. Which do you think is the...
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Assuming you have available both enantiomers of the amino acid valine, how would you
convert the iodide A shown below to the indicated carboxylic acid? You may assume other common
reagents and solvents needed are also available.
enantiosel.
OBn alkylation
OBn
H₂N
CO₂H
(valine)
Transcribed Image Text:1. Assuming you have available both enantiomers of the amino acid valine, how would you convert the iodide A shown below to the indicated carboxylic acid? You may assume other common reagents and solvents needed are also available. enantiosel. OBn alkylation OBn H₂N CO₂H (valine)
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