Abstract
(Chemical Equation Presented) Novel macrocycles possessing ether linkages and 2,6-disubstituted phenolics were produced in one step and with 100% atom economy by isoaromatization of chameleon macrocyclic precursors possessing 2,6-diarylidenecyclohexanone moieties. Intramolecular hydrogen bonding of the phenolic hydrogen atoms influenced the shape of the macrocycles and dictated host-guest behavior.
Original language | English |
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Pages (from-to) | 3261-3264 |
Number of pages | 4 |
Journal | Organic Letters |
Volume | 6 |
Issue number | 19 |
DOIs | |
Publication status | Published - 1 Sept 2004 |
Externally published | Yes |