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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 40, 2010 - Issue 15
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Original Articles

Facile Heteropolyacid-Promoted Synthesis of Indeno[1,2-b]quinoline-9,11(6H,10H)-dione Derivatives

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Pages 2191-2200 | Received 28 May 2009, Published online: 07 Jul 2010

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Read on this site (3)

Mohammad Bayat, Fahimeh Sadat Hosseini & Shima Nasri. (2018) An efficient one-pot synthesis of tetrahydrothiazolo[3,2-a]quinolin-6-one derivatives. Journal of Sulfur Chemistry 39:1, pages 99-111.
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Praveen Chidurala, Venkateshwarlu Jetti & Jyotsna S. Meshram. (2014) A green and convenient approach for the synthesis of 1,10-phenanthrolines via a catalyst- and solvent-free condition. Green Chemistry Letters and Reviews 7:2, pages 113-118.
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Articles from other publishers (14)

Shankar D. Dhengale, Chandrashekhar V. Rode, Govind B. Kolekar & Prashant V. Anbhule. (2022) Synthesis of indeno-[1,2- b ]-quinoline-9,11(6 H ,10 H )-dione and 7,7-dimethyl-10-aryl-7,8-dihydro-5 H -indeno[1,2- b ]quinoline-9,11(6 H ,10 H )-dione derivatives in presence of heterogeneous Cu/zeolite-Y as a catalyst . RSC Advances 12:4, pages 2083-2093.
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Fahimeh Sadat Hosseini & Mohammad Bayat. (2020) A simple method for the rapid synthesis of 2-amino-7,7-dimethyl-5-oxo-1,4-diaryl-hexahydroquinoline-3-carboxamide derivatives. Journal of the Iranian Chemical Society 17:9, pages 2267-2274.
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Ryhan Abdullah Rather & Zeba N. Siddiqui. (2019) Silver phosphate supported on metal–organic framework (Ag 3 PO 4 @MOF‐5) as a novel heterogeneous catalyst for green synthesis of indenoquinolinediones . Applied Organometallic Chemistry 33:11.
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Milad Masoumi, Fahimeh Sadat Hosseini & Mohammad Bayat. (2018) Synthesis of (E)-2-amino-N′-benzylidenehexahydroquinoline-3-carbohydrazide. Molecular Diversity 23:3, pages 593-601.
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Wen-Juan Yang, Jing Zhang, Jing Sun & Chao-Guo Yan. (2016) Convenient Construction of Indanedione-Fused 2,5-Dihydropyridines, 4,5-Dihydropyridines, and Spirooxindolines. European Journal of Organic Chemistry 2016:32, pages 5423-5428.
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Shima Asadi & Ghodsi Mohammadi Ziarani. (2015) The molecular diversity scope of 1,3-indandione in organic synthesis. Molecular Diversity 20:1, pages 111-152.
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Gong Jin, Jing Sun & Chao-Guo Yan. (2016) Formation of zwitterionic salts via three-component reaction of benzimidazolium bromides, aromatic aldehydes and 1,3-indanedione. RSC Advances 6:87, pages 84379-84387.
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Vijay V. Shinde, Mudumala Veeranarayana Reddy, Yong Hyun Kim, Byung Kwon Cho & Yeon Tae Jeong. (2014) Silica sodium carbonate: the most efficient catalyst for the one-pot synthesis of indeno[1,2-b]quinoline and spiro[chromene-4,3′-indoline]-3-carbonitriles under solvent-free condition. Monatshefte für Chemie - Chemical Monthly 146:4, pages 673-682.
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Majid M. Heravi & Zeinab Faghihi. (2013) Applications of heteropoly acids in multi-component reactions. Journal of the Iranian Chemical Society 11:1, pages 209-224.
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Yu-peng Liu, Jin-ming Liu, Xin Wang, Tie-ming Cheng & Run-tao Li. (2013) Multicomponent reactions leading to symmetric and asymmetric multi-substituted 1,4-dihydropyridines on montmorillonite. Tetrahedron 69:25, pages 5242-5247.
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Farhad Shirini, Somayyeh Sarvi Beigbaghlou, Seyyed Vahid Atghia & Seyyed Ali-Reza Mousazadeh. (2013) Multi-component one-pot synthesis of unsymmetrical dihydro-5H-indeno[1,2-b]quinolines as new pH indicators. Dyes and Pigments 97:1, pages 19-25.
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Shahrzad Abdolmohammadi. (2013) Simple route to indeno[1,2-b]quinoline derivatives via a coupling reaction catalyzed by TiO2 nanoparticles. Chinese Chemical Letters 24:4, pages 318-320.
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Nimesh M. Shah, Manish P. Patel & Ranjan G. Patel. (2012) New N-arylamino biquinoline derivatives: microwave-assisted synthesis and their antimicrobial activities. Medicinal Chemistry Research 22:1, pages 312-322.
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Majid M. Heravi, Hamideh Alinejhad, Khadijeh Bakhtiari, Zohreh Daroogheha, Fatemeh F. Bamoharram, Fatemeh Derikvand & Behnoush Alimadadi. (2010) ChemInform Abstract: Facile Heteropolyacid‐Promoted Synthesis of Indeno[1,2‐b]quinoline‐9,11(6H,10H)‐dione Derivatives.. ChemInform 41:52.
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