A dichotomy in the Friedel-Crafts reactions of lactones provides a convenient new route to 2-acylated pyrroles and tetrahydroindolones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference31 articles.
1. Die Synthese von aromatisch substituierten Säuren aus δ‐Chlor‐γ‐valerolacton, I. Mitteil.: Über die Friedel‐Craftssche Reaktion der Lactone
2. Condensation of Lactones with Benzene
3. Photochemical Transformations of 2,2-Dimethylspiro[4,5]deca-6,9-dien-8-one. Solvent Effects on the Stereochemistry of the Lumiketone Rearrangement
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1. ChemInform Abstract: A Dichotomy in the Friedel-Crafts Reactions of Lactones Provides a Convenient New Route to 2-Acylated Pyrroles and Tetrahydroindolones.;ChemInform;2010-08-13
2. Practical ex-chiral-pool methodology for the synthesis of dopaminergic tetrahydroindoles;Tetrahedron;2004-01
3. 5-Hydroxy[1,2]oxazinan-3-ones as potential carbapenem and D-ala-D-ala surrogates;Canadian Journal of Chemistry;2003-08-01
4. Facile synthesis of (S)-β-hydroxy-β-trichloromethylated aromatic ketones by the regioselective ring cleavage of chiral β-trichloromethyl-β-propiolactone under the Friedel-Crafts conditions;Tetrahedron Letters;1997-03
5. The thermal rearrangement of N-alkyl-N-vinylpropargylamines into 2-methylpyrroles. A new synthesis of annulated[b]pyrroles;Tetrahedron Letters;1996-09
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