7. The following reaction is from a synthesis of the natural product salinipyrone A. After being synthesized, salinipyrone A was then screened for antitumor activity. Predict the major product of this reaction. Note that the TBS-protected alcohol is stable to the Wittig reaction condition OTBS Me OTBS - 1-0-1-1-84 -t-Bu Me H Ph P=CHCO₂Et

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter18: Functional Derivatives Of Carboxylic Acids
Section: Chapter Questions
Problem 18.43P: The following sequence of steps converts (R)-2-octanol to (S)-2-octanol. Propose structural formulas...
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7. The following reaction is from a synthesis of the natural product salinipyrone A. After being
synthesized, salinipyrone A was then screened for antitumor activity. Predict the major product of this
reaction. Note that the TBS-protected alcohol is stable to the Wittig reaction condition
--1
الله
OTBS
Me
OTBS - 1-0-4-1-84
Si-t-Bu
Me
H
Ph₂P=CHCO₂Et
Transcribed Image Text:7. The following reaction is from a synthesis of the natural product salinipyrone A. After being synthesized, salinipyrone A was then screened for antitumor activity. Predict the major product of this reaction. Note that the TBS-protected alcohol is stable to the Wittig reaction condition --1 الله OTBS Me OTBS - 1-0-4-1-84 Si-t-Bu Me H Ph₂P=CHCO₂Et
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