The Birch reduction–dialkylation reaction. Scope and limitations
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. The Birch Reduction - Dialkylation Reaction of Aromatic Carboxylic Acids. Identification of NaNH2as the Base Responsible for the Second Alkylation
2. Unpublished results.
3. Alkylation of 1,5-dimethoxy-1,4-cyclohexadiene. A convenient synthesis of 2-alkyl- and 2-alkenyl-1,3-cyclohexanediones
4. A possible nucleophilic ipso-aromatic substitution with a benzyl anion as the leaving group
5. Perhydroindan derivatives. 17. Application of the reduction-methylation sequence to 7-methoxyhexahydrofluorene derivatives
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1. 8.19 Partial Reduction of Benzenoid Aromatic Rings by Dissolving Metals and by Other Methods;Comprehensive Organic Synthesis II;2014
2. Diastereoselective alkylation reactions of 1-methylcyclohexa-2,5-diene-1-carboxylic acid;Organic & Biomolecular Chemistry;2012
3. Transitions of Leading Rolling Research and Technology;Journal of the Japan Society for Technology of Plasticity;2011
4. Birch Reduction;Comprehensive Organic Name Reactions and Reagents;2010-09-15
5. Regioselective Arene Functionalization: Simple Substitution of Carboxylate by Alkyl Groups;Chemistry - A European Journal;2009-11-09
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