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

  • Vincent Huc
  • , Eloäne Npetgat
  • , Vincent Guérineau
  • , Sophie Bourcier
  • , Amandine Dos Santos
  • , Régis Guillot
  • , Jean Pierre Baltaze
  • , Cyril Martini

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Pages (from-to)6186-6192
Number of pages7
JournalEuropean Journal of Organic Chemistry
Issue number32
DOIs
Publication statusPublished - 1 Nov 2010
Externally publishedYes

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