Regioselectivity of methyl chlorobenzoate analogues with trimethylstannyl anions by radical nucleophilic substitution: theoretical and experimental study
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2010/NJ/B9NJ00664H
Reference20 articles.
1. Electron-transfer, halogen-metal exchange, and direct processes in formal nucleophilic substitutions on alkyl halides by trimethyltinsodium
2. Evidence for electron transfer in the reaction of (trimethylstannyl)sodium with primary alkyl halides
3. Electron transfer in the reactions of alkyl halides with sodium trimethylstannate
4. Reaction of (CH3)3SnM and Ph3SnM (M = lithium, sodium, potassium) with optically active 2-octyl tosylate, chloride, and bromide
5. Nucleophilic Substitution Reactions by Electron Transfer
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1. Synthesis of Aryl Trimethylstannane via BF3·OEt2-Mediated Cross-Coupling of Hexaalkyl Distannane Reagent with Aryl Triazene at Room Temperature;The Journal of Organic Chemistry;2018-12-12
2. Cobalt-Catalyzed Methoxycarbonylation of Substituted Dichlorobenzenes as an Example of a Facile Radical Anion Nucleophilic Substitution in Chloroarenes;Molecules;2014-05-06
3. Recent advances in the synthesis of stannanes and the scope of their posterior chemical transformations;Journal of Organometallic Chemistry;2014-02
4. Nucleophilic Aromatic Substitution;Organic Reaction Mechanisms Series;2012-12-04
5. Theoretical and experimental study on the reactivity of methyl dichlorobenzoates with sulfur-centered nucleophiles by electron transfer reactions;Tetrahedron;2012-01
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