Addition radicalaire de l’hydrure de tributylétain aux cétones α-cyclopropaniques et α-éthyléniques: mise en évidence d'un effet polaire
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference8 articles.
1. Reductions de cetones α-cyclopropaniques au moyen de l'hydrure de tributyletain
2. CCCLXXXVIII.—The nature of the alternating effect in carbon chains. Part XXII. An attempt further to define the probable mechanism of orientation in aromatic substitution
3. A Reëxamination of the Hammett Equation.
4. A simple re-evaluation of the hammett ϱσ relation
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1. One- and Two-Electron Reactions from the Rearrangement of α-Ketocyclopropanes by O-Stannyl Ketyls;The Journal of Organic Chemistry;1997-12-01
2. Regioselective Ring-opening of Cyclopropyl Ketones with Organometallic Reagents;Chemistry Letters;1997-11
3. Reactions of Tin(IV) Enolates and Radicals Derived from the Tin Hydride Scission of Cyclopropyl Ketones;The Journal of Organic Chemistry;1997-08-01
4. Radical Ion Probes. 3. The Importance of Resonance vs. Strain Energy in the Design of SET Probes Based upon the Cyclopropylcarbinyl-to-Homoallyl Radical Rearrangement;Journal of the American Chemical Society;1994-03
5. Radical ion probes. 2. Evidence for the reversible ring opening of arylcyclopropylketyl anions. Implications for mechanistic studies;Journal of the American Chemical Society;1992-02
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