## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Mass spectra of 3-phenyl-2,1-benzisoxazoles
✍ Scribed by Leonard K. Dyall; Gary J. Karpa
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 288 KB
- Volume
- 24
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
✦ Synopsis
We report here the electron impact (EI) mass spectra of eight 3-phenyi-2,l -benzisoxazoles (l), seven of which bear substituents in the benzo ring at positions 5 or 6. H 1 (Ph=C,H,) 2 a These two ions, C,, H, and CloH,N, could not be resolved from one another or from '2C,0'3C,H7. The experimental mass measurement corresponded to Cl0H,N. The B/E linked scan (see Fig. 2) indicates that M+' loses 55 mass units. This mass loss fits either or both of M -(CO + HCN) and M -(CO + H + C,H,).
📜 SIMILAR VOLUMES
## Abstract The mass spectra of a series of 2‐__p__‐substituted phenyl‐1,3,2‐dioxaborolanes have been examined and compared with the mass spectrum of 2‐phenyl‐1,3,2‐dioxaborolane. Formation of the substituted ion [C~7~H~6~X]^+^ by electron impact induced rearrangement has been found to be influence
Phenyl 2,3-unsaturated-O-glycosides are very interesting starting materials for the synthesis of a large variety of 2,3unsaturated-C-glycosides.' Mass spectral fragmentations of a wide variety of acetylated glycosides have been reported2-\* and some information on the relative differences in the ion
## Abstract The electron impact mass spectra of thirteen new substituted 2‐(__o__‐R^1^‐phenyl)‐indole‐3‐carboxaldehydes which have potentially useful pharmacological properties, ate presented.