Calculated energies for proton abstraction from substituted benzenes, and their significance for base cleavage of aryltrimethylsilanes
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference10 articles.
1. 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
2. Alkaline cleavage of substituted phenyltrimethylsilanes in aqueous dimethylsulphoxide
3. Aromatic reactivity. Part XLVI. Interpretation of the substituent effects in base-catalysed cleavage of aryltrimethyl-silanes and -stannanes
4. Molecular orbital theory of the electronic structure of organic compounds. I. Substituent effects and dipole moments
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1. Deprotonative C–H Silylation of Functionalized Arenes and Heteroarenes Using Trifluoromethyltrialkylsilane with Fluoride;Organic Letters;2015-01-30
2. Ruthenium-Catalyzed C–H Silylation of 1-Arylpyrazole Derivatives and Fluoride-Mediated Carboxylation: Use of Two Nitrogen Atoms of the Pyrazole Group;Synlett;2014-04-28
3. Electrophilic Reactions of Aryl- and Heteroaryl(triniethyl)silanes with a Remarkable Nucleophilic Catalysis;Angewandte Chemie International Edition in English;1981-03
4. Bemerkenswerte nucleophil katalysierte elektrophile Reaktionen von Aryl- und Heteroaryltrimethylsilanen;Angewandte Chemie;1981-03
5. The rates of base cleavage of substituted 2-thienyltrimethylsilanes. AB initio calculations of the acidities of monosubstituted thiophens;Journal of Organometallic Chemistry;1981-01
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