Synthesis of azaanthraquinone derivatives via a hetero diels-alder reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. A regioselective synthesis of 4,5- and 4,8- disubstitutedaza-anthraquinones by the diels-alder route
2. Umsetzungen von Dimethylhydrazonen ungesättigter Aldehyde mit elektrophilen Reagenzien
3. Diels-Alder cycloaddition of juglone derivatives: elucidation of factors influencing regiochemical control
4. Regiochemical control in Diels–Alder routes to aza-anthraquinone derivatives
5. Cycloaddition routes to azaanthraquinone derivatives. 2. Use of azadienes
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1. Metal-Free C–C Cross Coupling: Electrosynthesis of Azaheterocycles through Anodic Oxidation Cyclization of 1,6-Enynes;ACS Sustainable Chemistry & Engineering;2022-03-03
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3. Magnetite Nanoparticles-Supported APTES as a Powerful and Recoverable Nanocatalyst for the Preparation of 2-Amino-5,10-dihydro- 5,10-dioxo-4H-benzo[g]chromenes and Tetrahydrobenzo[g]quinoline-5,10- diones;Combinatorial Chemistry & High Throughput Screening;2017-03-23
4. Synthesis of Tetrahydrobenzo[ g ]Quinoline Derivatives Using Recoverable Carbonaceous Material as Heterogeneous Catalyst;Journal of Heterocyclic Chemistry;2017-01-19
5. Recent applications of the hetero Diels–Alder reaction in the total synthesis of natural products;RSC Advances;2015
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