抄録
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.
| 本文言語 | English |
|---|---|
| ページ（範囲） | 1337-1338 |
| ページ数 | 2 |
| ジャーナル | Chemistry Letters |
| 号 | 12 |
| DOI | |
| 出版ステータス | Published - 1999 |
ASJC Scopus subject areas
- 化学 (全般)