Ingold−Fischer “Persistent Radical Effect”, Solvent Effect, and Metal Salt Oxidation of Carbon-Centered Radicals in the Synthesis of Mixed Peroxides from tert-Butyl Hydroperoxide
- 13 June 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 62 (12), 3849-3857
- https://doi.org/10.1021/jo9700944
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- A Free-Radical Mechanism in a Novel Metalloporphyrin-Catalyzed Oxidation of Phenols by t-BuOOHChemistry Letters, 1996
- Free-Radical Mechanisms in the Oxidation and Halogenation of Alkanes, Alkenes and Alkylbenzenes by t-BuOOH under Gif-Barton CatalysisSynlett, 1996
- A Mechanistic Probe for Oxygen Activation by Metal Complexes and Hydroperoxides and Its Application to Alkane Functionalization by [FeIIICl2tris(2-pyridinylmethyl)amine]+ BF4-Journal of the American Chemical Society, 1995
- Hydroperoxides as pseudohalides: oxidation, oxidative alkylation, acylation and arylation of acrylonitrileJournal of the Chemical Society, Chemical Communications, 1995
- New syntheses of mixed peroxides under Gif–Barton oxidation of alkylbenzenes, conjugated alkenes and alkanes; a free-radical mechanismJournal of the Chemical Society, Chemical Communications, 1994
- Rates of decarboxylation of acyloxy radicals formed in the photocleavage of substituted 1-naphthylmethyl alkanoatesJournal of the American Chemical Society, 1991
- Alkane functionalization by nonporphyrin iron complexes: mechanistic insightsInorganic Chemistry, 1990
- Persistent carbon-centered radicalsAccounts of Chemical Research, 1976
- Absolute rate constants for hydrocarbon autoxidation. XV. The induced decomposition of some t-hydroperoxidesCanadian Journal of Chemistry, 1969
- Peresters. V.1 Di-t-butylperoxyoxalateJournal of the American Chemical Society, 1960