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
Structural and stereochemical factors in the mass spectrometry of mono- and dimethylbicyclo[3.3.1]nonanes
✍ Scribed by L. S. Golovkina; G. V. Rusinova; I. M. Sokolova; I. A. Matveeva; G. E. Gervitz; A. A. Petrov
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 565 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1076-5174
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## Abstract Mass spectral fragmentations of two cyclopentane, eight cyclohexane and four norbornane/one 1,3‐amino alcohols were studied under electron ionization (EI) by low‐resolution, high‐resolution, metastable ion analysis and collision‐induced dissociation (CID) techniques. All stereoisomeric
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