## Abstract Eleven structurally different α, β‐unsaturated ketones were subjected to the __Clemmensen__ reduction under anhydrous conditions using amalgamated zinc, hydrogen chloride in a solution of ethyl ether, and acetic anhydride. In all cases but one the formation of cyclopropyl acetates was o
✦ LIBER ✦
The mechanism of the reduction of α,β-unsaturated (steroid) ketones with diborane
✍ Scribed by Ian Midgley; Carl Djerassi
- Publisher
- Elsevier Science
- Year
- 1972
- Tongue
- French
- Weight
- 130 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Caglioti and coworkers have shown that certain a&unsaturated ketones react with excess diborane, and after hydrolysis of the organoborane intermediate with acetic anhydride, good yields of an alkene are obtained. 192 The reaction undoubtedly follows the course depicted in the Scheme: Scheme
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