| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1328173 | Journal of Organometallic Chemistry | 2007 | 6 Pages |
Abstract
The nucleophilic attack on the nitrogen-bound hydrogen of the imine results in elimination of alkane. The attack is preceded by fast migratory insertion equilibrium. Only methane elimination could be observed for the aryl-substitutes imines.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Alexander A. Aksenov, David E. Richardson, John R. Eyler,