A series of esters derived from syn-and anti-2-methyl-2-azabicyclo[2.2.2]octan-6-ols were synthesized and studied by NMR spectroscopy. The unambiguous assignment of all bicyclic proton and carbon resonances was achieved by the combined analysis of the COSY, 1 H-13 C correlation spectra and double re
Stereoselective hetero-Diels–Alder reactions: structure determination of new xanthenedione derivatives by NMR spectroscopy and x-ray crystallography
✍ Scribed by Anne Giraud; Patrice Vanelle; Luc Giraud
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 119 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
The proton and carbon spectra of chromane derivatives were completely assigned by the use of 1H, 13C and 2D NMR spectroscopy, including NOESY and 2D INADEQUATE. The unambiguous conÐgurational assignments of all regioisomers were achieved via 2D NOESY. The structure of the regioisomer 7A was conÐrmed using x-ray di †raction.
📜 SIMILAR VOLUMES
A series of esters derived from synand anti-2-methyl-2-azabicyclo [ 2.2.2 ] octan-5-ols were synthesized and studied by 1H, 13C and 2D NMR spectroscopy. The crystal structure of 5-syn-(3,5-dichlorobenzoyloxy)-2-methyl-2azabicyclo [ 2.2.2 ] octane was determined by x-ray di †raction. The unambiguous