## Abstract Temperatureโdependent ^1^Hโ and ^13^CโNMR spectra of the title compound are presented. Coalescence effects are discussed and assigned to two dynamic processes: (a) ring inversion of the nineโmembered ring, (b) racemization of the enantiomeric groundโstate conformations of the nineโmembe
Conformational Analysis of Nine-Membered Cyclic Acetals. Stereoelectronic Effect in 2,4- and 3,5-Benzodioxonine Derivatives
โ Scribed by Migda, Wojciech; Rys, Barbara
- Book ID
- 125986232
- Publisher
- American Chemical Society
- Year
- 2006
- Tongue
- English
- Weight
- 199 KB
- Volume
- 71
- Category
- Article
- ISSN
- 0022-3263
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๐ SIMILAR VOLUMES
The NW? spectra of compounds l-5, recorded at different temperatures, are discussed and interpreted in terms of conformational eguilibrium. Ground state conformations are found to be chiral, ring inversion barriers are surprisingly high (ca 48 kJ/mol).
The use of high-performance liquid chromatography in the reversed-phase mode coupled to a spectrophotofluorimetric detector allowed the selective detection of acidic indoles possessing a C-3 methylene side chain, following the reaction of a purified plant extract with acetic anhydride. Of these acid