Relative Reactivities of Alkyl Chlorides under Friedel‐Crafts Conditions
Author:
Affiliation:
1. Institut für Chemie, Medizinische Universität zu Lübeck, Ratzeburger Allee 160, 23538 Lübeck 1, F.R.G.
2. Institut für Organische Chemie, Technische Hochschule Darmstadt, Petersenstraβe 22, 64287 Darmstadt, F.R.G.
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19941270129
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1. Steuerung der relativen Elektrophilie von Alkylierungsmitteln durch Variation der Lewis-Säure-Konzentration
2. Control of the Relative Electrophilicity of Alkylating Agents by Variation of the Lewis Acid Concentration
3. Stepwise [2 + 2] and [3 + 2] "cycloaddition" reactions of allenyl cations with olefins
4. Scope and limitations of aliphatic Friedel-Crafts alkylations. Lewis acid catalyzed addition reactions of alkyl chlorides to carbon-carbon double bonds
5. Synthesis of adamantane derivatives. 49. Substitution reaction of 1-adamantyl chloride with some trimethylsilylated unsaturated compounds
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