FORMATION OF DIHYDROPEROXIDE DERIVATIVES DURING THE OXIDATION OF CYCLOHEXENE AND TETRALIN BY DIOXYGEN

Authors
DOMBI G EVANICS F JAKY K CSANYI LJ
Citation
G. Dombi et al., FORMATION OF DIHYDROPEROXIDE DERIVATIVES DURING THE OXIDATION OF CYCLOHEXENE AND TETRALIN BY DIOXYGEN, Reaction kinetics and catalysis letters, 63(2), 1998, pp. 241-244
Citations number
2
Categorie Soggetti
Chemistry Physical
Journal title
Reaction kinetics and catalysis letters → ACNP
ISSN journal
01331736
Volume
63
Issue
2
Year of publication
1998
Pages
241 - 244
Database
ISI
SICI code
0133-1736(1998)63:2<241:FODDDT>2.0.ZU;2-K
Abstract
H-1- and C-13-NMR investigations revealed that prolonged oxidation of unsubstituted cyclohexene and tetralin, containing symmetrical and wea k allylic and benzylic CH bonds, results in the formation of both mono - and dihydroperoxo derivatives.