During the lithiuw-liquid amonia reduction of an e,b-unsaturated ketone, the adaition of various alkyl halides leads to the forwation of a-alkylated ketones (1). We employed excess ethyl browoacetate as the alkylating species, and the yield (65%) was considerably more #an that expected. Vapor phase
β¦ LIBER β¦
Notes: Formation of Cyclopropane Derivatives from 4-Bromocrotonic Esters
β Scribed by Ratney, Ronald; English, James
- Book ID
- 125899772
- Publisher
- American Chemical Society
- Year
- 1960
- Tongue
- English
- Weight
- 395 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0022-3263
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