Abstract
Recognition of planar chirality of 14-hydroxy-12-oxabicyclo[9.2.2]pentadecane-1 (14), 11(15)-diene-1,13-dione (C8) and 16-hydroxy-14-oxabicyclo[11.2.2]heptadecane-1(16),13(17)-diene-2,15-dione (C10) by native and O-methylated cyclodextrins has been studied by NMR spectroscopy. The cyclodextrins prefer the (R)-enantiomers of C8 and C10, which might well fit with asymmetrically twisted cavities of cyclodextrins.
Original language | English |
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Pages (from-to) | 1337-1338 |
Number of pages | 2 |
Journal | Chemistry Letters |
Issue number | 12 |
DOIs | |
Publication status | Published - 1999 |
ASJC Scopus subject areas
- Chemistry(all)