OH 16,17-dehydroprogesterone

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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The biosynthesis of lanosterol from squalene has intrigued chemists
since its discovery. It is now possible, for example, to synthesize
polycyclic compounds from acyclic or monocyclic precursors by
reactions that form several C—C bonds in a single reaction mixture.
a.) Draw a stepwise mechanism for the following reaction.

b.) Show how X can be converted to 16,17-dehydroprogesterone.

OH
16,17-dehydroprogesterone
Transcribed Image Text:OH 16,17-dehydroprogesterone
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