Concentration and substrate dependent reaction mechanisms in the metal ketyl-alkyl halide system. Magnetochemical zero-order kinetics as evidence for a diamagnetic reactive species at high ketyl concentrations. Catalysis by transition metals-Reference-Cited by-同舟云学术

Concentration and substrate dependent reaction mechanisms in the metal ketyl-alkyl halide system. Magnetochemical zero-order kinetics as evidence for a diamagnetic reactive species at high ketyl concentrations. Catalysis by transition metals

Published:1975-01 Issue:6 Volume:16 Page:417-420
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Screttas Constantinos G.,Georgiou Demetra G.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference8 articles.

1. Effect of solvent on the reactivity of the benzophenone free radical anion

2. On the mechanism of ring metallation of aromatic compounds. Metallation of thiophen by lithium and by lithium dihydroarylides

3. Metallation of aryl ethers by lithium arenes

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1. Structural changes in concentrated solutions of alkali metal monosubstituted benzophenone radical anions as deduced from1H NMR measurements;Magnetic Resonance in Chemistry;2001

2. Stoichiometry of protonation of aromatic hydrocarbon radical anions by weak proton donors. A marked discrepancy between the number of protons used and those incorporated into the aromatic structure;Journal of Organometallic Chemistry;1996-04

3. Stoichiometry and mechanism of protonation of alkali metal salts of benzophenone radical anions by weak proton donors and its relevance to the base-catalyzed decomposition of benzopinacol;Russian Chemical Bulletin;1995-01

4. Cidnp study of reactions of ketyls and dianions derived from benzophenone and fluorenone with acetic anhydride;Tetrahedron;1984-01

5. Single-titration method for the determination of lithium naphthalenide in tetrahydrofuran;Journal of Organometallic Chemistry;1983-08