The Chemistry of Heterocyclic Compounds, Quinoxalines: Supplement II

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European Journal of Chemistry

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Prime members enjoy FREE Delivery on millions of eligible domestic and international items, in addition to exclusive access to movies, TV shows, and more. Back to top. Get to Know Us. English Choose a language for shopping. Audible Download Audio Books. Table 4 Comparison of the result in the reaction of 1,2-diphenylethanedione 1a with 1,2-diaminobenzene 2a with our method and the previous literature. Experimental Section 3. General Information Unless otherwise stated, all reagents and chemicals in this study were used as received and were not further purified Sigma-Aldrich Chemie GmbH, Taufkirchen, Germany.

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General Reaction Procedure To a mixture of 1,2-dicarbonyl compound 1a — e 1. Conclusions In summary, we have developed an environmentally friendly and highly active cobalt nanoparticle on mesoporous SBA material for the synthesis of quinoxalinesin excellent yields from 1,2-diamine and 1,2-dicarbonyl compounds. Acknowledgments F. Author Contributions F. Conflicts of Interest The authors declare no conflict of interest. Footnotes Sample Availability : Samples of the compounds 3a — l are available from the authors. References 1. Brown D.

The Chemistry of Heterocyclic Compounds. Quinoxalines: Supplement II. Katritzky A. Handbook of Heterocyclic Chemistry. Pergamon; Oxford, UK: Eicher T. The Chemistry of Heterocycles. Moorthy N. Mini Rev. Rong F. Parhi A.

Quinoxalines, Spplement 2 by Desmond J. Brown, Edward C. Taylor, Peter Wipf - smaragclocrentpror.ml

Antibacterial activity of quinoxalines, quinazolines, and 1,5-naphthyridines. Smits R. Fragment based design of new H 4 receptor-ligands with anti-inflammatory properties in vivo. Hazeldine S. Rajule R. Perturbing pro-survival proteins using quinoxaline derivatives: A structure—activity relationship study.

Quinoxalines, Spplement 2

Hui X. Synthesis and antiprotozoal activity of some new synthetic substituted quinoxalines. Kim Y. Synthesis and biological activity of new quinoxaline antibiotics of echinomycin analogues. Sessler J. Quinoxaline-Bridged Porphyrinoids. Azov V. Resorcin[4]arenecavitand-based molecular switches. Champion R.

Electronic properties and field-effect transistors of thiophene-based donor—acceptor conjugated copolymers. Rapid Commun. Wang E. An easily synthesized blue polymer for high-performance polymer solar cells. Chang D. Novel quinoxaline-based organic sensitizers for dye-sensitized solar cells. Zhang X.

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Zhuang W. Molecular orbital energy level modulation through incorporation of selenium and fluorine into conjugated polymers for organic photovoltaic cells. Wang K. Synthesis and photovoltaic properties of a D—A copolymer based on the 2,3-di 5-hexylthiophenyl quinoxaline acceptor unit. Chen S. Synthesis of two conjugated polymers as TNT chemosensor materials. Actuators B. Brock E. Reactive Dye Compounds. WO A1.

Aromatic heterocyclic compounds: Pyridine

Lindner B. N-fused quinoxalines and benzoquinoxalines as attractive emitters for organic light emitting diodes. Thomas K. Chromophore-labeled quinoxaline derivatives as efficient electroluminescent materials. Ayaz M. Novel succinct routes to quinoxalines and 2-benzimidazolylquinoxalines via the Ugi reaction.

Tetrahedron Lett. Srinivas C. Efficient, convenient and reusable polyaniline-sulfate salt catalyst for the synthesis of quinoxaline derivatives. A Chem. More S. Cerium IV ammonium nitrate CAN as a catalyst in tap water: A simple, proficient and green approach for the synthesis of quinoxalines. Green Chem. Bhosale R.

An efficient protocol for the synthesis of quinoxaline derivatives at room temperature using molecular iodine as the catalyst. Zhao Z. General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines. Jafarpour M. Easy access to quinoxaline derivatives using alumina as an effective and reusable catalyst under solvent-free conditions. A Gen. Mahesh R.

Citric acid: An efficient and green catalyst for rapid one pot synthesis of quinoxaline derivatives at room temperature. Magnetic Fe 3 O 4 nanoparticles as new, efficient, and reusable catalysts for the synthesis of quinoxalines in water. Niknam K.


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Silica bonded S -sulfonic acid: A recyclable catalyst for the synthesis of quinoxalines at room temperature. Cai J. Gallium III triflate-catalyzed synthesis of quinoxaline derivatives. Yadav J. Bismuth III -catalyzed rapid synthesis of 2,3-disubstituted quinoxalines in water. Hille T. The Synthesis of benzimidazoles and quinoxalines from aromatic diamines and alcohols by iridium-catalyzed acceptorless dehydrogenative alkylation. Cho C. A new ruthenium-catalyzed approach for quinoxalines from o -phenylenediamines and vicinal-diols. Jeena V. An environmentally friendly, cost effective synthesis of quinoxalines: The influence of microwave reaction conditions.

Sithambaram S. Manganese octahedral molecular sieves catalyzed tandem process for synthesis of quinoxalines.