Pure and Applied Chemistry

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• 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. <http://dx.doi.org/10.1016/j.molliq.2011.12.012>
• 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>
• 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>
• 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>
• 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>
• 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.: 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>