Enantioselective catalysis XXIII. Aminoalcohol assisted decarboxylation of 2-carboxy-2-methyl-1-tetralone leading to enantioenriched 2-methyl-1-tetralone
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Chemistry
Link
http://link.springer.com/content/pdf/10.1007/BF00807568.pdf
Reference22 articles.
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5. Mustapha N (1991) DEA. University of Reims
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1. Amino alcohol-mediated enantioselective syntheses of α-substituted indanones and tetralones, ammonium enolates as key intermediates;Tetrahedron: Asymmetry;2014-05
2. On the decarboxylation of 2-methyl-1-tetralone-2-carboxylic acid – oxidation of the enol intermediate by triplet oxygen;New Journal of Chemistry;2013
3. Organocatalyzed Enantioselective Protonation;Enantioselective Organocatalyzed Reactions I;2011
4. ChemInform Abstract: Enantioselective Catalysis. Part 23. Aminoalcohol Assisted Decarboxylation of 2-Carboxy-2-methyl-1-tetralone Leading to Enantioenriched 2-Methyl-1-tetralone.;ChemInform;2010-06-23
5. Asymmetric Malonic and Acetoacetic Acid Syntheses – A Century of Enantioselective Decarboxylative Protonations;European Journal of Organic Chemistry;2008-11
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