| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278096 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
Distal dialkoxy derivatives of calix[4]arene (RÂ =Â Me, Et, Pr, n-Bu) can be regioselectively deuterated at the para positions of unsubstituted phenolic rings using DCl/D2O in tetrachloroethane solution.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Michaela MaÄková, Michal Himl, Lenka MináÅová, Jan Lang, Pavel Lhoták,
![First Page Preview: Regioselective deuteration of 25,27-dialkoxycalix[4]arenes Regioselective deuteration of 25,27-dialkoxycalix[4]arenes](/preview/png/5278096.png)