The Carbon-13 Magnetic Resonance Spectrum of an Organic Peroxide
- 1 January 1975
- journal article
- research article
- Published by Taylor & Francis in Spectroscopy Letters
- Vol. 8 (8) , 547-550
- https://doi.org/10.1080/00387017508067358
Abstract
Phenanthrene ozonide and methanol combine under acid catalysis to produce a 1:1 adduct, mp 180–181°, assigned structure 1 on the basis of C-H analysis and infrared spectrum.1,2 Although β,β′-dihydroxyalkylperoxides have been isolated from equilibrium mixtures of aldehydes and hydrogen peroxide, they are rarely if ever as thermally stable as the phenanthrene ozonide:methanol adduct.3Keywords
This publication has 1 reference indexed in Scilit:
- The Ozonolysis of Phenanthrene in MethanolJournal of the American Chemical Society, 1956