Mass spectra and stereochemistry of alkylsubstituted 2,2-diphenyl-1,3-dioxa-2-germacyclohexanes
β Scribed by A. I. Gren; N. E. Yasinenko; O. S. Timofeev; D. V. Zagorevskii
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 241 KB
- Volume
- 21
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
β¦ Synopsis
The correlations between electron impact induced formation of fragment [M -C,&]+' from alkylsubstituted 2,2-diphenyl-1,3-dioxa-2-gennacyclohexane (1) and the peculiarities of the molecular structures were found. Benzene elimination is regiospecific and stereoselective, resulting from the abstraction of an axial phenyl group and a hydrogen atom from the C-4 or C-6 position of the ring.
π SIMILAR VOLUMES
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 ma
Recently, a route to 2,2-dihydro-5-imino-1,2-oxaphosphol-3-enes (1, 2) was re-
## Abstract The mass spectra of 20 1,3βdithianes were studied. The fragmentation patterns including the loss of 74 u and 107 u and clearage of the substituent at Cβ2 depended strongly on the nature of the substituents at that position. 2,2βDiphenylβ1,3βdithiane undergoes an atypical fragmentation i
A study of the fragmentation of 1-methyl-3-(2-benzothiazolyllhydrazono)-2-indolinone on electron impact reveals that the major processes involve N-N bond fission and the competing loss of CO from the molecular ion.