Abstract
This review describes the current position in the emerging field of direct synthesis of O-alkyl resorcarenes through the use of O-protected precursors. The use of this approach for the selective synthesis of the diastereoisomers of resorc[4]arenes, the synthesis of parent resorcarenes and pyrogalloranes and the preparation of chiral partially alkylated resorc[4]arenes are highlighted. The applications of such molecules, with regard to their role as ligand platforms, for binding of cations, organic electron acceptors and in chiral discrimination are discussed.
| Original language | English |
|---|---|
| Pages (from-to) | 137-155 |
| Number of pages | 19 |
| Journal | Journal of Inclusion Phenomena and Macrocyclic Chemistry |
| Volume | 65 |
| Issue number | 1-2 |
| DOIs | |
| Publication status | Published - 2009 |
Keywords
- C-UNALKYLATED CALIX<4>RESORCINARENE
- CONFORMATIONAL PROPERTIES
- O-alkyl resorcarenes
- BIS-CROWN ETHERS
- ENANTIOMERICALLY PURE
- Resorcinarenes
- STEREOISOMERS
- CATALYZED SYNTHESIS
- Calixarenes
- RECEPTORS
- HOST-GUEST CHEMISTRY
- C-4 SYMMETRIC RESORCINARENES
- GAS-PHASE
- Resorcarenes
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