(iv) Compound B can be prepared from carboxylic acid D. What reagent would you select in order to convert D into B? (v) Amino alcohol C can be prepared from epoxide E and amine F. Accordingly, show the retrosynthesis of C and then a mechanism for the forward reaction. obt schil Novocaine O₂N H₂N o O₂N OH O₂N B HO E HN.

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter22: Carbonyl Alpha-substitution Reactions
Section22.SE: Something Extra
Problem 64AP: The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold...
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(iv) Compound B can be prepared from carboxylic acid D. What reagent would you select in order
to convert D into B?
(v) Amino alcohol C can be prepared from epoxide E and amine F. Accordingly, show the
retrosynthesis of C and then a mechanism for the forward reaction.
شور تایوان
ل اور مالی
HaN
Novocaine
D
OH
ON
HO
C
E
HN.
F
Transcribed Image Text:(iv) Compound B can be prepared from carboxylic acid D. What reagent would you select in order to convert D into B? (v) Amino alcohol C can be prepared from epoxide E and amine F. Accordingly, show the retrosynthesis of C and then a mechanism for the forward reaction. شور تایوان ل اور مالی HaN Novocaine D OH ON HO C E HN. F
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