Abstract
Three isoxazoline tetracycles were obtained enantiomerically pure by intramolecular 1,3-dipolar cycloaddition. The characterization of the new compounds was performed by high-resolution 1H and 13C NMR spectroscopy. The relative configuration of the new chiral centers was determined by NOESY experiments and confirmed by single-crystal X-ray structural analysis. © 2002 Elsevier Science Ltd. All rights reserved.
Original language | English |
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Pages (from-to) | 2419-2425 |
Journal | Carbohydrate Research |
Volume | 337 |
Issue number | 24 |
DOIs | |
Publication status | Published - 29 Nov 2002 |
Keywords
- Intramolecular 1,3-dipolar cycloaddition
- Isoxazolines
- Stereocontrol, NMR spectroscopy
- X-Ray crystallography