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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 44, 2014 - Issue 13
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Synthetic Communications Reviews

Studies on Quinolinedione: Synthesis, Reactions, and Applications

Wafaa S. Hamama Chemistry Department, Faculty of Science, Mansoura University, Mansoura, EgyptCorrespondence[email protected]
,
Alaa El-Din E. Hassanien Chemistry Department, Faculty of Science, Mansoura University, Mansoura, Egypt
&
Hanafi H. Zoorob Chemistry Department, Faculty of Science, Mansoura University, Mansoura, Egypt
Pages 1833-1858 | Received 12 Nov 2013, Published online: 29 May 2014

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Liangliang Han & Zhongqiang Zhou. (2019) An efficient and green protocol for synthesis of novel [1,3]oxazino[5,6-c]quinolin-5-one derivatives using [Et3NH]HSO4 as a reusable catalyst. Synthetic Communications 49:16, pages 2044-2052.
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Articles from other publishers (14)

Yaseen A. M. M. Elshaier, Ashraf A. Aly, Mohamed Abd El-Aziz, Hazem M. Fathy, Alan B. Brown & Mohamed Ramadan. (2021) A review on the synthesis of heteroannulated quinolones and their biological activities. Molecular Diversity 26:4, pages 2341-2370.
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Ashraf A. Aly, Mohamed Ramadan, Gamal El-Din A. Abuo-Rahma, Yaseen A.M.M. Elshaier, Mohammed A.I. Elbastawesy, Alan B. Brown & Stefan Bräse. 2021. 147 196 .
Zizhen Yin, Yingjie Yu, Chunxiang Li, Haibo Mei, Kai Zhu & Jianlin Han. (2020) Sulfuration‐Triggered Radical Cyclization of o ‐Cyanoarylacrylamides to 3‐Thiomethylated Quinoline‐2,4‐dione . ChemistrySelect 5:46, pages 14534-14537.
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Eva Schütznerová, Adam Přibylka, Noelia S. Medran & Viktor Krchňák. (2020) Greening Solid-Phase Organic Synthesis: Environmentally Conscious Synthesis of Pharmaceutically Relevant Privileged Structures 5,6-Dihydropyridin-2(1 H )-ones and Quinolin-2(1 H )-ones . The Journal of Organic Chemistry 85:18, pages 11867-11881.
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Rabdan M. Tikhov & Nikolai Yu. Kuznetsov. (2020) Construction of piperidine-2,4-dione-type azaheterocycles and their application in modern drug development and natural product synthesis. Organic & Biomolecular Chemistry 18:15, pages 2793-2812.
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Sanberk S. Atalay, Meerna Y. Assad, Taro Amagata & Weiming Wu. (2020) Mild, efficient, and solvent-free synthesis of 4-hydroxy-2-quinolinones. Tetrahedron Letters 61:16, pages 151778.
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X. L. Yu, J. Y. Deng, J. F. Chen & H. Q. Yang. (2019) Prediction of 13C NMR Chemical Shifts of Quinolone Derivatives Based on DFT Calculations. Journal of Structural Chemistry 60:5, pages 772-779.
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Liangliang Han & Zhongqiang Zhou. (2019) ZrOCl 2 ·8H 2 O as an efficient and recyclable catalyst for the one-pot multicomponent synthesis of novel [1,3]oxazino[5,6-c]quinolin-5-one derivatives . Applied Organometallic Chemistry 33:4, pages e4755.
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Wafaa S. Hamama, Mona E. Ibrahim, Ayaa A. Gooda & Hanafi H. Zoorob. (2018) Efficient Synthesis, Antimicrobial, Antioxidant Assessments and Geometric Optimization Calculations of Azoles- Incorporating Quinoline Moiety. Journal of Heterocyclic Chemistry 55:11, pages 2623-2634.
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Wafaa S. Hamama, Mona E. Ibrahim, Ayaa A. Gooda & Hanafi H. Zoorob. (2018) Recent advances in the chemistry of 2-chloroquinoline-3-carbaldehyde and related analogs. RSC Advances 8:16, pages 8484-8515.
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Hong Fu, Shi-Sheng Wang & Ya-Min Li. (2016) Copper-Mediated Oxidative Radical Addition/Cyclization Cascade: Synthesis of Trifluoromethylated and Sulfonated Quinoline-2,4(1 H ,3 H )-diones . Advanced Synthesis & Catalysis 358:22, pages 3616-3626.
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Shucheng Wang, Xuhu Huang, Qi Wang, Zemei Ge, Xin Wang & Runtao Li. (2016) An efficient synthesis of sulfonated quinoline diones by copper catalyzed sulfonylation of activated alkenes with sulfonylhydrazides. RSC Advances 6:14, pages 11754-11757.
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Shi-Sheng Wang, Hong Fu, Guanlin Wang, Meng Sun & Ya-Min Li. (2016) Iron-catalyzed addition/cyclization cascade of activated alkenes with alcohols: access to carbonyl substituted quinoline-2,4-diones. RSC Advances 6:57, pages 52391-52394.
Crossref
Wafaa S. Hamama, Alaa El‐Din E. Hassanien & Hanafi H. Zoorob. (2014) ChemInform Abstract: Studies on Quinolinedione: Synthesis, Reactions, and Applications. ChemInform 45:32.
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