Mass spectra of certain initiators of radical reactions and resonance capture of slow electrons by 2-cyanoisopropyl and tert-butoxyl radicals
β Scribed by R. G. Kostyanovskii; V. I. Khvostenko; I. I. Furlei; A. P. Pleshkova
- Book ID
- 112437079
- Publisher
- Springer
- Year
- 1974
- Tongue
- English
- Weight
- 302 KB
- Volume
- 23
- Category
- Article
- ISSN
- 1573-9171
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Hydrogen atom abstraction rate constants for the reaction of tert-butoxyl and 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical with the HMG-CoA reductase inhibitors lovastatin, simvastatin, and statins I-IV were measured. This series of diene-containing drugs is known to be prone to oxidation. The tert-
The 9,10-dicyanoanthracene-photosensitized (DCA-photosensitized) electron-transfer reaction of 1-isopropylidene-2methylene-3,3-diphenylcyclobutane (3) gives a mixture of the [4 + 4] DCA adduct (5) and two [4 + 4] cyclodimers Scheme 1