The Grignard Reagent Formation Reaction of 2-Chloro-1,1,1-triphenylethane Revisited
โ Scribed by Friedrich Bickelhaupt; Martin Newcomb; Christopher B. DeZutter; Henk J. R. de Boer
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 173 KB
- Volume
- 2008
- Category
- Article
- ISSN
- 1434-193X
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๐ SIMILAR VOLUMES
The Grignard reagent from racemic l-chloro-2-phenylbutane has been partially resolved by allowing it to react with less than one equivalent of one of several readily available chiral ketones. Reaction with approximately 0.5 equivalents(2) of (+)-camphor, (-)-fenchone, (-)-menthone or (+)-3-methylcyc
Asymmetric reductions with the Grignard reagent from optically active lchloro-2-phenylbutane have been studied by Mosher and coworkers. (1) We wish
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