Rearrangements accompanying the fragmentation of ionized 1-phenylalkan-1-ols
β Scribed by H. Budzikiewicz; G. Drabner; Ch. Hammes
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 310 KB
- Volume
- 28
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
β¦ Synopsis
Some aspects of the fragmentation sequence of 1-phenylalkan-1-01s (C,H,CH(OH)R), which consists of the loss of R' followed by the elimination of CO and subsequently of H , , are discussed. Labelling studies and collision activation data of reference compounds allow a mechanism to be proposed for this rearrangement.
π SIMILAR VOLUMES
## Abstract The electron impact mass spectra of 1βphenylβ2βpropenβ1βol and its specifically deuterated analogues have been investigated. Most of the decomposition pathways involve skeletal rearrangements or hydrogen atom transfers, such that a rearrangement of the excited molecular ions of 1βphenyl