Stereochemistry of the Michael addition. An interesting solvent effect
✍ Scribed by R.A. Abramovitch; D.L. Struble
- Publisher
- Elsevier Science
- Year
- 1966
- Tongue
- French
- Weight
- 234 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The Michael Addition has usually been studied under conditions such and J. M. Muchowski. Can. J Chem 3f& 557 (1960). U A* No.3 2. Correct analyzes were obtained for all the new compounds mentioned here. Reaction mixtures were analyzed quantitatively and qualitatively by gas-liquid chromatography.
📜 SIMILAR VOLUMES
b) R. F. Hudson and M. Green, Angew. Chem. Internat. Edit. & 11 (1963).
## Abstract A proline‐catalyzed asymmetric Michael addition between ketones and __trans__‐β‐nitrostyrene was studied by using the density‐functional theory with mPW1PW91 and B3LYP functionals. Improved insight into the enantio‐ and diastereoselective formation of γ‐nitroketones/‐aldehydes is obtain
## Abstract For Abstract see ChemInform Abstract in Full Text.