Mn(OAc)3 catalyzed intermolecular oxidative peroxycyclization of naphthoquinone
Author:
Affiliation:
1. Aix-Marseille Université
2. CNRS
3. Institut de Chimie Radicalaire ICR
4. UMR 7273
5. Laboratoire de Pharmaco-Chimie Radicalaire
6. Chemistry Department
7. Faculty of Science
8. Assiut University
9. Egypt
Abstract
Manganese(iii) acetate mediated peroxycyclization between 2-hydroxy-3-methylnaphthoquinone and alkenes allowed the synthesis of more than 50 original dihydronaphtho[2,3-c][1,2]dioxine-5,10(3H,10aH)-diones.
Funder
Aix-Marseille Universite
Centre National de la Recherche Scientifique
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/RA/C6RA25138B
Reference48 articles.
1. Rapid Syntheses of Biologically Active Quinazolinone Natural Products Using Microwave Technology
2. Manganese(III)-Based Oxidative Free-Radical Cyclizations
3. Manganese(III) Mediated Reactions of Unsaturated Systems
4. Synthesis of dihydrofuro- and C-alkenylated naphthoquinones catalyzed by manganese(III) acetate
5. Formation of 1,2-dioxacyclohexanes by the reaction of alkenes with tris(2,4-pentanedionato)manganese(III) or with β-ketocarbonyl compounds in the presence of manganese(III) acetate
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