The effect of additives and solvents on the hydrogenolysis of 2-methyl-2-phenylaziridine derivatives with palladium catalyst
β Scribed by Sekio Mitsui; Yoshihiro Sugi
- Publisher
- Elsevier Science
- Year
- 1969
- Tongue
- French
- Weight
- 227 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
In the previous paper (l), we reported the stereoselectivity of several Group VIII transition metal catalysts on the hydrogenolysis of 2-methyl-2-phenylaziridine and suggested that the configuration of the product is determined by the free energy difference of the transition states to form the carbon metal bond, which depends on the affinity of the catalyst for the nitrogen,
π SIMILAR VOLUMES
## Abstract Density functional theory calculations with the B3LYP functional were performed for the title ringβopening reaction to understand the intrinsic activating and directing effects of the __N__βsubstituents, as well as the electron donating effect of the paraβsubstituted (Y = Cl, H, Me) phe