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Journal ArticleDOI

Nucleophilic character of alkyl radicals—IX : The benzyl radical

Angelo Clerici, +2 more
- 01 Jan 1973 - 
- Vol. 29, Iss: 18, pp 2775-2779
TLDR
In this paper, homolytic benzylation of 4-substituted pyridines gives 1,2-diphenylethane and a benzyl-4-substantituted Pyridine in a ratio determined by the nature of the 4substituents.
About
This article is published in Tetrahedron.The article was published on 1973-01-01. It has received 16 citations till now. The article focuses on the topics: Radical & Homolysis.

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Citations
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Book ChapterDOI

Recent aspects of homolytic aromatic substitutions

TL;DR: The homolytic substitution acquires a more significant weight in the field of the aromatic substitutions, characterized by high selectivity and versatility.
Journal ArticleDOI

Nucleophilic character of alkyl radicals—XII : Mechanism and new syntheses in the oxidation of alcohols by peroxydisulphate

TL;DR: In this article, the authors investigated the mechanism of the oxidation of alcohols by peroxydisulphate by trapping the nucleophilic carbon-centered free-radical intermediates by protonated quinoline.
Journal ArticleDOI

Darstellung C-4-substituierter Pyridazine durch homolytische Alkylierung bzw. Acylierung

TL;DR: In this article, the structures of 4,5-dibenzoyl-pyridazine were proved by 1H-NMR, IR, and mass spectra.
References
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Journal ArticleDOI

Free radicals by mass spectrometry. XLIL Ionization potentials and ionic heats of formation for C1—C4 alkyl radicals

TL;DR: Ionization potentials for C1-C4 alkyl free radicals have been re-measured by electron impact, using an energy-resolved electron beam from a double-hemispherical electrostatic monochromator as mentioned in this paper.
Journal ArticleDOI

Free Radicals by Mass Spectrometry. XLIII. Ionization Potentials and Ionic Heats of Formation for Vinyl, Allyl, and Benzyl Radicals

TL;DR: Using an energy-resolved electron beam, ionization potentials for the following free radicals have been measured: vinyl 8.95 V, allyl 8.07 V, benzyl 7.27 V as mentioned in this paper.
Journal ArticleDOI

Nucleophilic character of alkyl radicals—VII : Substituent effects on the homolytic alkylation of protonated heteroaromatic bases with methyl, primary, secondary and tertiary alkyl radicals

TL;DR: In this paper, the relative rates of the homolytic alkylation of protonated 4-substituted pyridines with methyl, n-propyl and n-butyl radicals, obtained by the silver-catalyzed decarboxylation of acids with ammonium peroxydisulphate, are reported.
Journal ArticleDOI

Nucleophilic character of alkyl radicals—VIII : Kinetics and mechanism of induced decomposition of decanoyl peroxide in the homolytic alkylation of protonated quinoline

TL;DR: In this article, the thermal decomposition of decanoyl peroxide in benzene, heptane, quinoline, acetic add, and acetic acid was studied.
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