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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 40, 2010 - Issue 22
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Original Articles

Expeditious Pechmann Condensation by Using Biodegradable Cellulose Sulfuric Acid as a Solid Acid Catalyst

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Pages 3358-3364 | Received 04 Aug 2009, Published online: 15 Oct 2010

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Read on this site (4)

Leila Moradi, Khadijeh Rabiei & Fateme Belali. (2016) Meglumine sulfate catalyzed solvent-free one-pot synthesis of coumarins under microwave and thermal conditions. Synthetic Communications 46:15, pages 1283-1291.
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B. Suresh Kuarm, PeterA. Crooks & B. Rajitha. (2013) An expeditious synthesis of quinoxalines by using biodegradable cellulose sulfuric acid as a solid acid catalyst. Green Chemistry Letters and Reviews 6:3, pages 228-232.
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B. Suresh Kuarm, J. Venu Madhav, S. Vijaya Laxmi, B. Rajitha, Y. Thirupathi Reddy, P. Narsimha Reddy & PeterA. Crooks. (2011) Cellulose Sulfuric Acid: An Efficient Biodegradable and Recyclable Solid Acid Catalyst for the Synthesis of 1-Oxo-hexahydroxanthene. Synthetic Communications 41:12, pages 1719-1724.
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B. Suresh Kuarm, J. Venu Madhav, B. Rajitha, Y. Thirupathi Reddy, P. Narsimha Reddy & PeterA. Crooks. (2011) Cellulose Sulfuric Acid: Novel and Efficient Biodegradable and Recyclable Acid Catalyst for the Solid-State Synthesis of Thiadiazolo Benzimidazoles. Synthetic Communications 41:5, pages 662-669.
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Articles from other publishers (12)

Suresh Kuarm Bowroju, Hanumaiah Marumamula & Rajitha Bavanthula. (2021) Synthesis of 2-(2-oxo-2H-chromen-3-yl)-3-phenylquinazolin-4(3H)-ones as potent antimicrobial and antitubercular agents. Chemical Data Collections 35, pages 100744.
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Shalini Agarwal, Ankit Lathwal & Mahendra Nath. (2021) Recent Advances on Cellulose Sulfuric Acid as Sustainable and Environmentally Benign Organocatalyst for Organic Transformations. Current Organocatalysis 8:1, pages 72-92.
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Suresh Kuarm Bowroju, Hanumaiah Marumamula & Rajitha Bavanthula. (2021) Design and Synthesis of 11H-Xantheno[2,1-c][1,2,5]Selenadiazol-11-One Derivatives as Potent Antimicrobial and Antitubercular Agents. Russian Journal of Bioorganic Chemistry 47:2, pages 593-600.
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Jong-Wha Jung, Nam-Jung Kim, Hwayoung Yun & Young Han. (2018) Recent Advances in Synthesis of 4-Arylcoumarins. Molecules 23:10, pages 2417.
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Soma Shekar Dachavaram, Narsimha R. Penthala, Julie L. Calahan, Eric J. Munson & Peter A. Crooks. (2018) Highly sulphated cellulose: a versatile, reusable and selective desilylating agent for deprotection of alcoholic TBDMS ethers. Organic & Biomolecular Chemistry 16:33, pages 6057-6062.
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Souad Bouasla, Juan Amaro-Gahete, Dolores Esquivel, M. López, César Jiménez-Sanchidrián, Mabrouk Teguiche & Francisco Romero-Salguero. (2017) Coumarin Derivatives Solvent-Free Synthesis under Microwave Irradiation over Heterogeneous Solid Catalysts. Molecules 22:12, pages 2072.
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Suresh Maddila, Mehbub Momin, Palakondu Lavanya & Chunduri V. Rao. (2016) An efficient and eco-friendly synthesis of 6-chloro-8-substituted-9H-purines using cellulose sulfuric acid as a reusable catalyst under solvent-free conditions. Journal of Saudi Chemical Society 20:2, pages 173-177.
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Majid M. Heravi, Soheila Khaghaninejad & Manizhe Mostofi. 2014. 1 50 .
Jeffrey T. Kohrt, Ed Conn, Robert Maguire, Stephen W. Wright & Robert Singer. (2013) Expedient synthesis of novel β-ketoesters from the Mizoroki–Heck coupling of ethyl 3-ethoxyacrylate with aryl and pyridyl halides. Tetrahedron Letters 54:51, pages 7065-7068.
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G.M. Nazeruddin, M.S. Pandharpatte & K.B. Mulani. (2012) PEG-SO3H: A mild and efficient recyclable catalyst for the synthesis of coumarin derivatives. Comptes Rendus Chimie 15:1, pages 91-95.
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S. Vijaya Laxmi & B. Rajitha. (2010) Synthesis and antimicrobial activity of newer indole semicarbazones. Medicinal Chemistry Research 21:1, pages 85-90.
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B. Suresh Kuarm, J. Venu Madhav, S. Vijaya Laxmi, B. Rajitha, Y. Thirupathi Reddy, P. Narsimha Reddy & Peter A. Crooks. (2011) ChemInform Abstract: Expeditious Pechmann Condensation by Using Biodegradable Cellulose Sulfuric Acid as a Solid Acid Catalyst.. ChemInform 42:16.
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