Sequential acetalization-pyrolysis of α-acetyl benzalacetones. A method for the generation of 6-substituted 2-acetonaphthones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Synthesis of 2,6-bis(fluoroalkyl)-2,6-dihydroxytetrahydro-2H-pyran-3,5-dicarboxylates from aldehydes and fluorinated β-oxo esters in the presence of ionic liquid-K2CO3 as catalytic system;Russian Journal of Organic Chemistry;2010-04
2. Reaction of aromatic aldehydes with β-dicarbonyl compounds in a catalytic system: Piperidinium acetate-1-butyl-3-methylimidazolium tetrafluoroborate ionic liquid;Russian Chemical Bulletin;2005-05
3. Liquid phase acetylation of thioanisole with acetic anhydride to 4-(methylthio) acetophenone (4-MTAP) using H-beta catalyst;Catalysis Communications;2004-11
4. Anhydrous hydrogen fluoride catalyzed Friedel-Crafts reactions of thioaromatic compounds;The Journal of Organic Chemistry;1991-09
5. Sequential acetalization-pyrolysis of .alpha.-acetylcinnamates and .alpha.-acetylbenzalacetones. A method for the generation of 2-carbonyl-substituted naphthalenes;The Journal of Organic Chemistry;1990-01
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