| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5385105 | Chemical Physics Letters | 2010 | 5 Pages |
Abstract
⺠In this article we found that nucleofugality in nucleophilic substitution reactions may be determined by the permanent group to a significant extent. This information is of relevant to discuss both, the stability of the intermediate in a stepwise pathway; and also on the reaction mechanism. Nucleofugality is represented here on a quantitative basis and the usefulness of the reported conclusions may be of importance for the experimental chemists.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Paola R. Campodónico, Rodrigo Ormazábal-Toledo, Arie Aizman, Renato Contreras,