Calculations of the deprotonation energies of mono-substituted benzenes, and their significance for the mechanisms of base-catalysed cleavages of aryl-silicon and aryl-tin bonds and hydrogen-exchange in substituted benzenes-Reference-Cited by-同舟云学术

Calculations of the deprotonation energies of mono-substituted benzenes, and their significance for the mechanisms of base-catalysed cleavages of aryl-silicon and aryl-tin bonds and hydrogen-exchange in substituted benzenes

Published:1981-01 Issue:1 Volume:204 Page:27-45
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:en
Short-container-title:Journal of Organometallic Chemistry

Author:

Eaborn Colin,Stamper John G.,Seconi Giancarlo

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference33 articles.

1. Cleavage of diphenylmethyl-, triphenylmethyl-, fluoren-9-yl-, and substituted benzyl-trialkylstannanes by methanolic sodium methoxide. Evidence for a duality of mechanism

2. Aromatic reactivity. Part LXI. Reactivities and solvent isotope effects in the base cleavage of triorgano-silicon, -germanium, and -tin groups from furan, thiophen, benzofuran, and benzothiophen rings

3. The reaction of bis(phenyldimethylphosphine)bis(diphenylsilyl)platinum(II) with acetylenes

4. Alkaline cleavage of substituted phenyltrimethylsilanes in aqueous dimethylsulphoxide

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