Mass spectrometry in stereochemical problems. 6 — The case of mono and di-substituted norbornanes
✍ Scribed by O. Curcuruto; D. Favrctto; P. Traldi; D. Ajo; C. Cativiela; J. A. Mayoral; M. P. Lorez; J. M. Fraile; J. I. Garcia
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 455 KB
- Volume
- 26
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
✦ Synopsis
The mass spectrometric hehaviour of pairs of stereoisomeric moo* and &-substituted norbornanes, namely bicyclo [ 2.2.1 1 heptane-&ndo-and -exo-carboxylic acid, methyl bicyclo [ 2.2.1 1 heptane->endo-and -emcarboxylate, &xo-acetamidobicyclo [ 2.2.1 I heptaoe-2-endo-and Zendu-acetamidobicyclo 12.2.1 1 heptaoe-2-exocarboxylic acid and methyl 2-exo-acetamidobicyclo [ 2.2.1 1 heptane-2-endo-and Zendo-acetamido-bicycloI2.2.11 heptane-2-exo-carboxylate was studied in detail with particular emphasis on characterization of the stereoisomers. The fragmentation patterns, studied with the aid of mass-analysed ion kinetic energy spectrometry, were supported by semi-empirical M W F C calculations, performed using the AM1 method included in the AMPAC program.
📜 SIMILAR VOLUMES
IN continuation of our studies3 on the alkaloidal constituents of Brazilian Aspidosperma species, we have investigated the stem bark of Aspidosperma album (Vahl) R. Bent., which was collected in Manaus, Amaronas. The non-phenolic portion yielded the lcnown alkaloid4 (-)-quebmchamine, while from the
Following the demonstrations by Meyerson and coworkers4 and Rinehart et al 5 i.-' that the M-l ion in the mass spectrum of toluene is best represented OS a tmpylium structure, analogous ring expansion pathways have been proposed to rationalize data from l3 C-labeled compounds in the quinoline, indol