Abstract
A detailed investigation of the 4-(benzyloxy)phenol/formaldehyde reaction shows that along with the previously described p-(benzyloxy)calix[8]arene and p-(benzyloxy)calix[6]arene, others calixarenes are observed and easily recovered on a preparative scale. All these new calixarenes are opening interesting perspectives for the synthesis of new supramolecular hosts, easily functionalized at the para position under very mild conditions and/or exhibiting a deep hydrophobic pocket. During the course of the synthesis of p-(benzyloxy)calix[8]arene, compounds 4-7 are easily recovered as byproducts on a preparative scale. Alkylation of these new calixarenes leads to the first functionalized derivatives.
| Original language | English |
|---|---|
| Pages (from-to) | 6186-6192 |
| Number of pages | 7 |
| Journal | European Journal of Organic Chemistry |
| Issue number | 32 |
| DOIs | |
| Publication status | Published - 1 Nov 2010 |
| Externally published | Yes |
Keywords
- Alkylation
- Calixarenes
- Functionalization
- Supramolecular chemistry
Fingerprint
Dive into the research topics of 'P-(benzyloxy)calix[8]arene synthesis revisited: P-(benzyloxy)calix[4]-, p-(benzyloxy)calix[5]-, p-(benzyloxy)calix[7]-, and p-(benzyloxy)bis(homooxa) calix[4]arenes'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver