The Birch Reduction - Dialkylation Reaction of Aromatic Carboxylic Acids. Identification of NaNH2as the Base Responsible for the Second Alkylation
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919108019789
Reference13 articles.
1. Metal-Ammonia Reduction of Aromatic Molecules
2. Birch, A. J. and Subba Rao, G. 1972.“Advance in organic chemistry, methods and results”, Edited by: Taylor, E. C. Vol 8, 1–65. New York: Wiley-Interscience Publishers.
3. Synthesis of compounds related to gibberellic acid. III. Analogs of ring A of the gibberellins
4. Reduction of alkyl-substituted benzoic acids with lithium in liquid ammonia: Synthesis of 1-alkyl-2,5-cyclohexadiene-1-carboxylic acids
5. A New Route to 2-(β-Phenylethyl)-3-methyl-Δ2-cyclohexenones1
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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. Birch Reduction;Comprehensive Organic Name Reactions and Reagents;2010-09-15
3. The Birch reduction–dialkylation reaction. Scope and limitations;Tetrahedron Letters;2006-02
4. Structure of 1,4-diethyl-3,5-dimethoxy-1,4-dihydrobenzoic acid;Acta Crystallographica Section C Crystal Structure Communications;1993-07-15
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