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 |
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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