| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1409124 | Journal of Molecular Structure | 2012 | 4 Pages |
Abstract
⺠An unprecedented tris-substituted calix[4]arene derivative was synthesized. ⺠Steric hindrance and weak intramolecular interactions are key factors. ⺠The quite up-field aromatic chemical shift means the extremely rigid structure.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Unusually rigid macrocyclic tris(picolinolato)-4-tert-butylcalix[4]arene: Its intramolecular interaction effect on picolinoylation](/preview/png/1409124.png "First Page Preview: Unusually rigid macrocyclic tris(picolinolato)-4-tert-butylcalix[4]arene: Its intramolecular interaction effect on picolinoylation")
Authors
Haeri Lee, Tae Hwan Noh, Eun Ji Kim, Ok-Sang Jung,