| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5394482 | Computational and Theoretical Chemistry | 2012 | 4 Pages |
Abstract
⺠The conformational isomerism of a series of bromoalkoxycyclohexanes has been determined computationally. ⺠Isodesmic reactions were carried out to evaluate the preferred orientation of Br in an alkoxycyclohexane. ⺠Intramolecular interactions induced by substituents rule the conformational preferences.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Josué M. Silla, Matheus P. Freitas,