Pure and Applied Chemistry

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• Kaur Navjeet: Microwave-assisted synthesis of five-membered S-heterocycles. J IRAN CHEM SOC 2014, 11, 523. <http://dx.doi.org/10.1007/s13738-013-0325-2>
• Shirini Farhad, Yahyazadeh Asieh, Mohammadi Kamal: One-pot synthesis of various xanthene derivatives using ionic liquid 1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient and reusable catalyst under solvent-free conditions. Chinese Chemical Letters 2014, 25, 341. <http://dx.doi.org/10.1016/j.cclet.2013.11.016>
• Properzi Roberta, Marcantoni Enrico: Construction of heterocyclic structures by trivalent cerium salts promoted bond forming reactions. Chem. Soc. Rev. 2014, 43, 779. <http://dx.doi.org/10.1039/c3cs60220f>
• Mohamed Nadia R., Khaireldin Nahed Y., Fahmy Amin F., El-Sayed Ahmed A.: The Utility of Carbon Disulphide and Lawesson's Reagent for Synthesis of Different Fused Heterocycles for Antimicrobial Evaluation. J. Heterocyclic Chem. 2013, 50, 1264. <http://dx.doi.org/10.1002/jhet.884>
• Sachdeva Harshita, Dwivedi Diksha, Arya Kapil, Khaturia Sarita, Saroj Rekha: Synthesis, anti-inflammatory activity, and QSAR study of some Schiff bases derived from 5-mercapto-3-(4′-pyridyl)-4H-1,2,4-triazol-4-yl-thiosemicarbazide. Med Chem Res 2013, 22, 4953. <http://dx.doi.org/10.1007/s00044-013-0507-6>
• Fodor Kinga-Judit, Kocsis Vasile-Ludovic, Kiss Kolos, Károlyi Benedek-Imre, Szabolcs Ármin, Silaghi-Dumitrescu Luminita, Csámpai Antal: Comparative evaluation of a Pictet–Spengler protocol in microwave-assisted conversions of tryptamine with aryl- and carboxyaryl aldehydes: role of ring strain in cyclocondensation of the primarily formed carboxyaryl-substituted β-carbolines. Monatsh Chem 2013, 144, 1381. <http://dx.doi.org/10.1007/s00706-013-1007-6>
• Voloshko A. Yu., Pinchukova N. A., Shishkin O. V., Chebanov V. A.: Physical and Chemical Factors in Microwave-Accelerated Drying of Temperature-Sensitive Organic Compounds. Theor Exp Chem 2013, 49, 204. <http://dx.doi.org/10.1007/s11237-013-9316-8>
• Zare Abdolkarim, Abi Fereshteh, Moosavi-Zare Ahmad Reza, Beyzavi Mohammad Hassan, Zolfigol Mohammad Ali: Synthesis, characterization and application of ionic liquid 1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient catalyst for the preparation of hexahydroquinolines. Journal of Molecular Liquids 2013, 178, 113. <http://dx.doi.org/10.1016/j.molliq.2012.10.045>
• Dolzhenko Anton V., Kalinina Svetlana A., Kalinin Dmitrii V.: A novel multicomponent microwave-assisted synthesis of 5-aza-adenines. RSC Adv. 2013, 3, 15850. <http://dx.doi.org/10.1039/c3ra41932k>
• Zare Abdolkarim, Kaveh Hamideh, Merajoddin Maria, Moosavi-Zare Ahmad Reza, Hasaninejad Alireza, Zolfigol Mohammad Ali: Saccharin Sulfonic Acid (SASA) as a Highly Efficient Catalyst for the Condensation of 2-Naphthol With Arylaldehydes and Amides (Thioamides or Alkyl Carbamates) Under Green, Mild, and Solvent-Free Conditions. Phosphorus, Sulfur, and Silicon and the Related Elements 2013, 188, 573. <http://dx.doi.org/10.1080/10426507.2012.692131>
• Chavan A. V., Somani R. R., Kalantri P. P., Makhija D. T.: Rapid and Economic Access to Some NSAIDS-Based Bioactive Heterocycles. Journal of Chemistry 2013, 2013, 1. <http://dx.doi.org/10.1155/2013/785753>
• Zare Abdolkarim, Moosavi-Zare Ahmad Reza, Merajoddin Maria, Zolfigol Mohammad Ali, Hekmat-Zadeh Tahereh, Hasaninejad Alireza, Khazaei Ardeshir, Mokhlesi Mohammad, Khakyzadeh Vahid, Derakhshan-Panah Fatemeh: Ionic liquid triethylamine-bonded sulfonic acid {[Et3N–SO3H]Cl} as a novel, highly efficient and homogeneous catalyst for the synthesis of β-acetamido ketones, 1,8-dioxo-octahydroxanthenes and 14-aryl-14H-dibenzo[a,j]xanthenes. J Mol Liqs 2012, 167, 69. <http://dx.doi.org/10.1016/j.molliq.2011.12.012>
• Cui Zi-Ning, Shi Yan-Xia, Zhang Li, Ling Yun, Li Bao-Ju, Nishida Yoshihiro, Yang Xin-Ling: Synthesis and Fungicidal Activity of Novel 2,5-Disubstituted-1,3,4-oxadiazole Derivatives. J. Agric. Food Chem. 2012, 60, 11649. <http://dx.doi.org/10.1021/jf303807a>
• Daştan Arif, Kulkarni Aditya, Török Béla: Environmentally benign synthesis of heterocyclic compounds by combined microwave-assisted heterogeneous catalytic approaches†. Green Chem 2012, 14, 17. <http://dx.doi.org/10.1039/c1gc15837f>
• Zare Abdolkarim, Akbarzadeh Shayesteh, Foroozani Elmira, Kaveh Hamideh, Moosavi-Zare Ahmad Reza, Hasaninejad Alireza, Mokhlesi Mohammad, Beyzavi Mohammad Hassan, Zolfigol Mohammad Ali: Triethylamine-bonded sulfonic acid ([Et 3N–SO 3H]Cl): a highly efficient and homogeneous catalyst for the condensation of 2-naphthol with arylaldehydes and amides (alkyl carbamates or thioamides). Journal of Sulfur Chemistry 2012, 33, 259. <http://dx.doi.org/10.1080/17415993.2012.690415>
• Ferreira Sabrina Baptista, Kaiser Carlos Roland: Pyrazine derivatives: a patent review (2008 – present). Expert Opin. Ther. Patents 2012, 22, 1033. <http://dx.doi.org/10.1517/13543776.2012.714370>
• Thummanagoti Suman, Yellol Gorakh S., Sun Chung-Ming: Microwave-Assisted Tandem Transformation on an Ionic-Liquid Support: Efficient Synthesis of Pyrrolo/Pyridobenzimidazolones and Isoindolinone-Fused Benzimidazoles. Chem —Asian J 2011, 6, 2471. <http://dx.doi.org/10.1002/asia.201100277>
• Ma Ning, Lu Han, Wu Feiyue, Zhang Ge, Jiang Bo, Shi Feng, Gao Yuan, Tu Shujiang: Green chemistry approach to the synthesis of 2-aryl-4-ferrocenyl-quinoline derivatives under microwave irradiation. J  Heterocycl Chem 2011, 48, 803. <http://dx.doi.org/10.1002/jhet.594>
• Bourhis Kevin, Blanc Sylvie, Mathe Carole, Dupin Jean-Charles, Vieillescazes Catherine: Spectroscopic and chromatographic analysis of yellow flavonoidic lakes: Quercetin chromophore. Appl Clay Sci 2011, 53, 598. <http://dx.doi.org/10.1016/j.clay.2011.05.009>
• Miklós Ferenc, Fülöp Ferenc: “Dry” and “Wet” Green Synthesis of 2,2′-Disubstituted Quinazolinones. Eur J Org Chem 2010, 2010, 959. <http://dx.doi.org/10.1002/ejoc.200901052>
• De Rosa Margherita, Soriente Annunziata: Rapid and General Protocol towards Catalyst-Free Friedel-Crafts C-Alkylation of Indoles in Water Assisted by Microwave Irradiation. Eur J Org 2010, 2010, 1029. <http://dx.doi.org/10.1002/ejoc.200901333>
• Heller Eberhard, Klöckner Jessica, Lautenschläger Werner, Holzgrabe Ulrike: Online Monitoring of Microwave-Enhanced Reactions by UV/Vis Spectroscopy. Eur J Org Chem 2010, 2010, 3569. <http://dx.doi.org/10.1002/ejoc.201000441>
• Polshettiwar Vivek, Varma Rajender S.: Nano-organocatalyst: magnetically retrievable ferrite-anchored glutathione for microwave-assisted Paal–Knorr reaction, aza-Michael addition, and pyrazole synthesis. Tetrahedron 2010, 66, 1091. <http://dx.doi.org/10.1016/j.tet.2009.11.015>
• De Rosa Margherita, Soriente Annunziata: A combination of water and microwave irradiation promotes the catalyst-free addition of pyrroles and indoles to nitroalkenes. Tetrahedron 2010, 66, 2981. <http://dx.doi.org/10.1016/j.tet.2010.02.055>
• Upadhyay Sunil K., Pingali Subramanya R.K., Jursic Branko S.: Comparison of microwave-assisted and conventional preparations of cyclic imides. Tetrahetron Lett 2010, 51, 2215. <http://dx.doi.org/10.1016/j.tetlet.2010.02.092>
• Polshettiwar Vivek, Varma Rajender S.: Green chemistry by nano-catalysis. Green Chem 2010, 12, 743. <http://dx.doi.org/10.1039/b921171c>
• Strauss Christopher Roy, Rooney David W.: Accounting for clean, fast and high yielding reactions under microwave conditions. Green Chem 2010, 12, 1340. <http://dx.doi.org/10.1039/c0gc00024h>
• Cahill Katharine J., Ajaz Aida, Johnson Richard P.: New Thermal Routes to ortho-Benzyne. Aust J Chem 2010, 63, 1007. <http://dx.doi.org/10.1071/CH10074>
• Kappe C. Oliver, Dallinger Doris: Controlled microwave heating in modern organic synthesis: highlights from the 2004–2008 literature. Mol Divers 2009, 13, 71. <http://dx.doi.org/10.1007/s11030-009-9138-8>
• Chen Yu, Markina Nataliya A., Larock Richard C.: An efficient, microwave-assisted, one-pot synthesis of indoles under Sonogashira conditions. Tetrahedron 2009, 65, 8908. <http://dx.doi.org/10.1016/j.tet.2009.07.075>
• Pastorin Giorgia, Dolzhenko Anna V., Chui Wai Keung, Dolzhenko Anton V.: An aqueous medium synthesis and tautomerism study of 3(5)-amino-1,2,4-triazoles. Tetrahetron Lett 2009, 50, 2124. <http://dx.doi.org/10.1016/j.tetlet.2009.02.172>
• Polshettiwar Vivek, Varma Rajender S.: Revisiting the Meerwein–Ponndorf–Verley reduction: a sustainable protocol for transfer hydrogenation of aldehydes and ketones. Green Chem 2009, 11, 1313. <http://dx.doi.org/10.1039/b913079a>
• Dicks Andrew P.: Solvent-free reactivity in the undergraduate organic laboratory. Green Chem Lett & Revs 2009, 2, 87. <http://dx.doi.org/10.1080/17518250903164549>
• Polshettiwar Vivek, Varma Rajender S.: ChemInform Abstract: Greener and Expeditious Synthesis of Bioactive Heterocycles Using Microwave Irradiation. ChemInform 2008, 39. <http://dx.doi.org/10.1002/chin.200838265>
• Polshettiwar Vivek, Varma Rajender S.: Pd–N-heterocyclic carbene (NHC) organic silica: synthesis and application in carbon–carbon coupling reactions. Tetrahedron 2008, 64, 4637. <http://dx.doi.org/10.1016/j.tet.2008.02.098>
• Polshettiwar Vivek, Varma Rajender S.: Aqueous microwave chemistry: a clean and green synthetic tool for rapid drug discovery. Chem Soc Rev 2008, 37, 1546. <http://dx.doi.org/10.1039/b716534j>
• Varma Rajender S.: Chemical activation by mechanochemical mixing, microwave and ultrasonic irradiation. Green Chem 2008, 10, 1129. <http://dx.doi.org/10.1039/b817559b>