A study of diastereoseleetive 1,4-addition of phenyl Grignard has been attempted on some chiral crotonates. The H-facial seleetivities in these reactions have been determined on the basis of specific rotations of the hydrolysis product, namely 3-phenyl butanoic acid (3PBA). Correlation of these resu
β¦ LIBER β¦
Determination of the Absolute Stereochemistry of Chiral Amines by 1H NMR of Arylmethoxyacetic Acid Amides: The Conformational Model
β Scribed by Latypov, Shamil K.; Seco, Jose M.; Quinoa, Emilio; Riguera, Ricardo
- Book ID
- 120034972
- Publisher
- American Chemical Society
- Year
- 1995
- Tongue
- English
- Weight
- 1021 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0022-3263
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