Hydroborationoxidation of pinene (page 213), like catalytic hydrogenation, is stereoselective. Addition takes place at the less hindered

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Hydroboration–oxidation of pinene (page 213), like catalytic hydrogenation, is stereoselective. Addition takes place at the less hindered face of the double bond, and a single alcohol is produced in high yield (89%). Suggest a reasonable structure this alcohol.
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Organic Chemistry

ISBN: 978-0072905014

4th edition

Authors: Francis A. Carey

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