Regioselective alkylation of a methylene group via meta-bridging of calix[4]arenes†
Petr Slavík,Hana Dvořáková,Václav Eigner,Pavel Lhoták
Chemical Communications Pub Date : 07/14/2014 00:00:00 , DOI:10.1039/C4CC04356A
Abstract

The meta-iodo derivative, fixed in the cone conformation, enables the gram-scale preparation of a meta-bridged calix[4]arene. This intermediate, possessing a fluorene moiety within the macrocyclic skeleton, can be regioselectively alkylated on the corresponding methylene bridge to form a unique substitution pattern in classical calixarene chemistry.

Graphical abstract: Regioselective alkylation of a methylene group via meta-bridging of calix[4]arenes