3. Propose an efficient synthesis for the target molecule from the indicated starting material. Assume you have a good selection of other reagents including any inorganic compounds, benzene, and any organic compound containing 3 or fewer carbons. Make sure your synthesis provides a way to control the relative stereochemistry of the target molecule (but not the absolute stereochemistry). Write both a retrosynthetic analysis and the synthesis in the forward direction showing all necessary reagents and reaction conditions for each step. Me Ph OH Ph target Me Me ད starting material

3. Propose an efficient synthesis for the target molecule from the indicated starting material. Assume you have a good selection of other reagents including any inorganic compounds, benzene, and any organic compound containing 3 or fewer carbons. Make sure your synthesis provides a way to control the relative stereochemistry of the target molecule (but not the absolute stereochemistry). Write both a retrosynthetic analysis and the synthesis in the forward direction showing all necessary reagents and reaction conditions for each step. Me Ph OH Ph target Me Me ད starting material

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

Chapter11: Ethers, Epoxides, And Sulfides

Section: Chapter Questions

Problem 11.42P

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