Explain why the hydrogen and the methyl substituent are trans to one another after photochemical ring closure of provitamin D3 to form 7-dehydrocholesterol.
Explain why the hydrogen and the methyl substituent are trans to one another after photochemical ring closure of provitamin D3 to form 7-dehydrocholesterol.
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
Chapter23: Amines
Section: Chapter Questions
Problem 23.60P: Following is a retrosynthesis for the coronary vasodilator ganglefene. (a) Propose a synthesis for...
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Explain why the hydrogen and the methyl substituent are trans to one another after photochemical ring closure of provitamin D3 to form 7-dehydrocholesterol.
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