Production and reduction of alkyl radicals under controlled, homogenous conditions through reactions of alkyl flourides with sodium naphthalenide. Rate constant for cyclization of 5-hexenyl radicals.
- 31 December 1969
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 10 (7) , 587-590
- https://doi.org/10.1016/s0040-4039(01)87755-8
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Reactions of aromatic radical anions. III. Evidence for an alkyl radical-radical anion combination mechanism for alkylation of sodium naphthalenide with alkyl halidesJournal of the American Chemical Society, 1968
- Radical mechanism of alkylation of sodium naphthalenideJournal of the American Chemical Society, 1968
- Homoallylic free radicals. A study of the rearrangement of 3,5-cyclocholestanyl radical to cholesteryl radicalJournal of the American Chemical Society, 1968
- Kinetics of the reduction of tert-butyl chloride and tert-butyl bromide by organotin hydridesJournal of the American Chemical Society, 1968
- Reactions of Aromatic Radical Anions. I. Coupling of Alkyl Free Radicals Generated by Electron Transfer to Alkyl Iodides1Journal of the American Chemical Society, 1966
- Radical Cyclizations in the Reaction of Trialkyltin Hydrides with Alkenyl Halides1Journal of the American Chemical Society, 1966
- Electron-Transfer Reaction of Radical Anions with Cholesteryl and Cyclocholestanyl ChloridesJournal of the American Chemical Society, 1966
- Some Stable Monoboron Free Radicals. 2,2'-Bipyridine Stabilization of Unusual Oxidation States of Boron1Journal of the American Chemical Society, 1966
- Effect of solvent on the reactivity of the benzophenone free radical anionTransactions of the Faraday Society, 1966
- The reactions of organic halides with organo-sodium complexes in solutionTransactions of the Faraday Society, 1955