Abstract
As an extension of earlier EPR studies of the radicals formed from acyclic olefinic substrates with the use of the TiC1 3H 2O 2 radical-generating method, results are presented of an analogous TiC1 3H 2O 2-based investigation carried out over the temperature range 10–40°C with the use of cyclic unsaturated substrates in acidified aqueous solution, namely, Δ 2-dihydrofuran, Δ 2-dihydropyran, 2-methylfuran, 2-acetylfuran, and furfurylamine. The EPR spectra of six radicals produced from these cyclic substrates are reported.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
