3.) The strategy for the synthesis shown below uses an acetal as a protecting group. a. Fill in the missing reagents or compounds for this synthesis. CH3 HO OH (1 equivalent) H-A Н. OH CH3 CH3 H OH CH3

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter24: Amines And Heterocycles
Section24.SE: Something Extra
Problem 68AP: Fill in the missing reagents a-e in the following scheme:
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please explain w steps both a and b
monitored to ensure that only the desired product is formed. Explain why the acetal
3b. The first step of the synthesis uses a limited quantity of the diol, and is carefully
formation occurs regioselectively at the carbonyl shown.
mainsdasM
Transcribed Image Text:monitored to ensure that only the desired product is formed. Explain why the acetal 3b. The first step of the synthesis uses a limited quantity of the diol, and is carefully formation occurs regioselectively at the carbonyl shown. mainsdasM
3.) The strategy for the synthesis shown below uses an acetal as a protecting group.
a. Fill in the missing reagents or compounds for this synthesis.
CH3
HO OH
(1 equivalent)
H-A
OH
CH3
CH3
H.
OH
CH3
Transcribed Image Text:3.) The strategy for the synthesis shown below uses an acetal as a protecting group. a. Fill in the missing reagents or compounds for this synthesis. CH3 HO OH (1 equivalent) H-A OH CH3 CH3 H. OH CH3
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