The configuration at C-2 and C-4 in the molecules of 2-methyl-and 1,2-dimethyl-4-vinylethinyl(n-butyl)-4-hydroxyperhydroquinolines was determined by mass spectrometry The principal conclusions concerning the stereochemistry were made on the basis of differences in the values of the I[H-151+/I[xl+.,
Mass spectrometric determination of the configuration of the 4-substituted 1,2-dimethyl-4-hydroxydecahydroquinolines
✍ Scribed by V. G. Zaikin; N. S. Wulfson; V. I. Zaretskii; A. A. Bakaev; A. A. Akhrem; L. I. Ukhova; N. F. Uskova
- Publisher
- John Wiley and Sons
- Year
- 1969
- Tongue
- English
- Weight
- 320 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
The mass spectra of a number of the epimeric 1,2-dimethyl-4-alkyl-4-hydroxydecahydroquinolines (alkyl: C z C H , CH=CH,, C,H, and COCH,) have been studied. The configuration at C-2 and C-4 in these molecules is proposed on the basis of the data obtained. Some aspects of the fragmentation pathways under electron-impact are discussed.
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## Abstract The configurations of 1,4:3,6‐dianhydro‐2,5‐di‐__O__‐mesyl‐D‐mannitol, 1,4:3,6‐dianhydro‐2,5‐di‐__O__‐mesyl‐D‐glucitol, 1,4:3,6‐dianhydro‐2,5‐di‐__O__‐mesyl‐L‐iditol, 1,4:3:6‐dianhtydro‐2‐deoxy‐2‐iodo‐5‐__O__‐mesyl‐D‐mannitol, 1,4:3:6‐dianhtydro‐2‐deoxy‐2‐iodo‐5‐__O__‐mesyl‐D‐glucitol,
## Abstract For Abstract see ChemInform Abstract in Full Text.