Pure and Applied Chemistry

CrossRef Cited-by Linking

• Gawande Manoj B., Bonifácio Vasco D. B., Luque Rafael, Branco Paula S., Varma Rajender S.: Solvent-Free and Catalysts-Free Chemistry: A Benign Pathway to Sustainability. ChemSusChem 2014, 7, 24. <http://dx.doi.org/10.1002/cssc.201300485>
• Pagadala Ramakanth, Gandhare Nilesh V., Kusampally Uppalaiah, Jetti Venkateshwarlu, Meshram Jyotsna S., Juneja H. D.: Synthesis of 1H -Imidazoles Catalyzed by Cu-Nanoparticle and Its Physicochemical Properties. J. Heterocyclic Chem. 2014, 51, 116. <http://dx.doi.org/10.1002/jhet.1551>
• Sturm Guido S.J., Verweij Martin D., Stankiewicz Andrzej I., Stefanidis Georgios D.: Microwaves and microreactors: Design challenges and remedies. Chemical Engineering Journal 2014, 243, 147. <http://dx.doi.org/10.1016/j.cej.2013.12.088>
• Pasnoori Srinivas, Kamatala Chinna Rajanna, Mukka Satish Kumar, Kancharla Rajendar Reddy: Prussian Blue as an Eco-Friendly Catalyst for Selective Nitration of Organic Compounds Under Conventional and Nonconventional Conditions. Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 2014, 44, 364. <http://dx.doi.org/10.1080/15533174.2013.770759>
• Wang Chang, Liu Jing, Leng Wenguang, Gao Yanan: Rapid and Efficient Functionalized Ionic Liquid-Catalyzed Aldol Condensation Reactions Associated with Microwave Irradiation. IJMS 2014, 15, 1284. <http://dx.doi.org/10.3390/ijms15011284>
• Iyyaswami Regupathi, Halladi Venkatesh Kamath, Yarramreddy Satyanarayana Reddy, Malur Bharathaiyengar Saidutta: Microwave-assisted batch and continuous transesterification of karanja oil: process variables optimization and effectiveness of irradiation. Biomass Conv. Bioref. 2013, 3, 305. <http://dx.doi.org/10.1007/s13399-013-0080-8>
• Basu Pradipta Kumar, Ghosh Amrita: Microwave promoted improved regioselective synthesis of 1H,3H,6H[2]benzopyrano[4,3-d]pyrimidine-2,4-diones by radical cyclisation. J IRAN CHEM SOC 2013, 10, 55. <http://dx.doi.org/10.1007/s13738-012-0171-7>
• Zaini Muhammad Abbas Ahmad, Kamaruddin Mohd Johari: Critical issues in microwave-assisted activated carbon preparation. Journal of Analytical and Applied Pyrolysis 2013, 101, 238. <http://dx.doi.org/10.1016/j.jaap.2013.02.003>
• Chang Wonghil, Shin Jihye, Chae GeumHee, Jang So Ra, Ahn Byoung Joon: Microwave-assisted Sonogashira cross-coupling reaction catalyzed by Pd-MCM-41 under solvent-free conditions. Journal of Industrial and Engineering Chemistry 2013, 19, 739. <http://dx.doi.org/10.1016/j.jiec.2012.11.002>
• Krishnaiah G., Sandeep B., Kondhare D., Rajanna K.C., Narendar Reddy J., Rajeshwar Rao Y., Zhubaidha P.K.: Manganese(II) salts as efficient catalysts for chemo selective transesterification of β-keto esters under non-conventional conditions. Tetrahedron Letters 2013, 54, 703. <http://dx.doi.org/10.1016/j.tetlet.2012.12.030>
• Rajendar Reddy K., Rajanna K.C., Uppalaiah K.: Environmentally benign contemporary Friedel–Crafts acylation of 1-halo-2-methoxynaphthalenes and its related compounds under conventional and nonconventional conditions. Tetrahedron Letters 2013, 54, 3431. <http://dx.doi.org/10.1016/j.tetlet.2013.04.075>
• Arya Kapil, Prabhakar Biswajeet: Ionic liquid confined zeolite system: an approach towards water mediated room temperature synthesis of spiro[pyrazolo[3,4-e]benzothiazepines]. Green Chem. 2013, 15, 2885. <http://dx.doi.org/10.1039/c3gc40553b>
• Izquierdo Diana F., Bernal Juana M., Burguete M. Isabel, García-Verdugo Eduardo, Lozano Pedro, Luis Santiago V.: An efficient microwave-assisted enzymatic resolution of alcohols using a lipase immobilised on supported ionic liquid-like phases (SILLPs). RSC Adv. 2013, 3, 13123. <http://dx.doi.org/10.1039/c3ra42467g>
• Long Yuhua, Zhang Haifeng, Yang Dingqiao: Efficient Synthesis of Ferrocenylquinolines via the Friedländer Reaction. Synthetic Communications 2013, 43, 619. <http://dx.doi.org/10.1080/00397911.2010.519090>
• Kumar M. Satish, Reddy K. Rajendar, Rajanna K. C., Venkanna P., Krishnaiah G.: Oxalylchloride/DMF as an Efficient Reagent for Nitration of Aromatic Compounds and Nitro Decarboxylation of Cinnamic Acids in Presence of KNO3 or NaNO2 Under Conventional and Nonconventional Conditions. Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 2013, 43, 977. <http://dx.doi.org/10.1080/15533174.2012.752395>
• Sedunova P. A., Artamonova T. V., Ramsh S. M.: Microwave synthesis of the TOTO and BOBO fluorescent probes. Russ Chem Bull 2012, 61, 847. <http://dx.doi.org/10.1007/s11172-012-0118-2>
• Raval Jignesh P., Desai Krunal G., Desai Kishor R.: Microwave synthesis, characterization and antimicrobial study of new pyrazolyl-oxopropyl-quinazolin-4(3H)-one derivatives. Journal of Saudi Chemical Society 2012, 16, 387. <http://dx.doi.org/10.1016/j.jscs.2011.02.003>
• Yadav Ganapati D., Devendran Saravanan: Lipase catalyzed kinetic resolution of (±)-1-(1-naphthyl) ethanol under microwave irradiation. Journal of Molecular Catalysis B: Enzymatic 2012, 81, 58. <http://dx.doi.org/10.1016/j.molcatb.2012.05.007>
• Neelakandeswari N., Sangami G., Emayavaramban P., Karvembu R., Dharmaraj N., Kim Hak Yong: Mesoporous nickel hydroxyapatite nanocomposite for microwave-assisted Henry reaction. Tetrahedron Letters 2012, 53, 2980. <http://dx.doi.org/10.1016/j.tetlet.2012.03.086>
• Baig R. B. Nasir, Varma Rajender S.: Alternative energy input: mechanochemical, microwave and ultrasound-assisted organic synthesis. Chemical Society Review 2012, 41, 1559. <http://dx.doi.org/10.1039/c1cs15204a>
• Rosana Michael R., Tao Yuchuan, Stiegman Albert E., Dudley Gregory B.: On the rational design of microwave-actuated organic reactions. Chem Sci 2012, 3, 1240. <http://dx.doi.org/10.1039/c2sc01003h>
• Raval Jignesh P., Naik Bhanvesh N., Desai Kishor R.: A Convenient, Rapid Microwave-Assisted Synthesis of 2-Substituted Phenyl-2,3-Dihydrobenzo[B][1,4]Thiazepine-3-Carboxamide Derivatives and Its Antimicrobial Activity. Phosphorus Sulfur Silicon Relat Elements 2012, 187, 255. <http://dx.doi.org/10.1080/10426507.2011.597800>
• Varghese Anitha, Nizam Aatika, Kulkarni Rajani, George Louis: Amberlite IR-120H: An improved reusable solid phase catalyst for the synthesis of nitriles under solvent free microwave irradiation. Eur. J. Chem. 2012, 3, 247. <http://dx.doi.org/10.5155/eurjchem.3.2.247-251.571>
• Charville Hayley, Jackson David A., Hodges George, Whiting Andrew, Wilson Mark R.: The Uncatalyzed Direct Amide Formation Reaction - Mechanism Studies and the Key Role of Carboxylic Acid H-Bonding. Eur J Org Chem 2011, 2011, 5981. <http://dx.doi.org/10.1002/ejoc.201100714>
• Sontakke Jyoti B., Yadav Ganapati D.: Optimization and kinetic modeling of lipase catalyzed enantioselective N-acetylation of ( ± )-1-phenylethylamine under microwave irradiation. J Chem Technol Biotechnol 2011, 86, 739. <http://dx.doi.org/10.1002/jctb.2582>
• Desai Krunal G., Naik Jiten I., Raval Jignesh P., Desai Kishor R.: Microwave-induced and conventional heterocyclic synthesis: An antimicrobial entites of newer quinazolinyl-Δ2-pyrazolines. ARAB J CHEM 2011. <http://dx.doi.org/10.1016/j.arabjc.2011.06.015>
• Borah Juri Moni, Chowdhury Pritish: Expedited Baeyer–Villiger oxidation of steroidal ketones by microwave irradiation. Steroid 2011, 76, 1341. <http://dx.doi.org/10.1016/j.steroids.2011.06.014>
• Ali Asraf A., Gaikar Vilas G.: Microwave-Assisted Process Intensification of Synthesis of Thymol Using Carbonized Sulfonic Acidic Resin (CSA) Catalyst. Ind Eng Chem Res 2011, 50, 6543. <http://dx.doi.org/10.1021/ie102053f>
• Lu Cheng-Rong, Zhao Bei, Jiang Ying-Peng, Ding Hao, Yang Sheng: One-Pot Synthesis of Salicylanilides by Direct Amide Bond Formation from Salicyclic Acid Under Microwave Irradiation. Synthetic Communications 2011, 41, 1257. <http://dx.doi.org/10.1080/00397911.2010.481745>
• Mouquinho Ana, Saavedra Mara, Maiau Alexandre, Petrova Krasimira, Barros M. Teresa, Figueirinhas J. L., Sotomayor João: Films Based on New Methacrylate Monomers: Synthesis, Characterisation and Electro-Optical Properties. Mol Liq Cryst 2011, 542, 132/[654]. <http://dx.doi.org/10.1080/15421406.2011.570154>
• Teresa Barros M., Mouquinho Ana I., Petrova Krasimira T., Saavedra Mara D., Sotomayor João C.: Fast synthesis employing a microwave assisted neat protocol of new monomers potentially useful for the preparation of PDLC films. cent eur j chem 2011, 9, 557. <http://dx.doi.org/10.2478/s11532-011-0046-2>
• Marvi Omid, Alizadeh Abdolhamid, Zarrabi Saeid: Montmorillonite K-10 Clay as an Efficient Reusable Heterogeneous Catalyst for the Solvent-Free Microwave Mediated Synthesis of 5-Substituted 1H-Tetrazoles. Bull Kor Chem Soc 2011, 32, 4001. <http://dx.doi.org/10.5012/bkcs.2011.32.11.4001>
• Loupy Andre, Perreux Laurence, Liagre Marion, Burle Karine, Moneuse Michel: ChemInform Abstract: Reactivity and Selectivity under Microwaves in Organic Chemistry. Relation with Medium Effects and Reaction Mechanisms. ChemInform 2010, 32, no. <http://dx.doi.org/10.1002/chin.200138269>
• Rodrigues Rafael C., Fernandez-Lafuente Roberto: Lipase from Rhizomucor miehei as a biocatalyst in fats and oils modification. Mol Catal B Enzym 2010, 66, 15. <http://dx.doi.org/10.1016/j.molcatb.2010.03.008>
• Kamath Venkatesh, Regupathi I, Saidutta MB: Microwave-assisted batch synthesis of Pongamia biodiesel. Biofuels 2010, 1, 847. <http://dx.doi.org/10.4155/bfs.10.66>
• 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>
• Jung Dai-Il, Song Ju-Hyun, Lee Eon-Jin, Kim Yun-Young, Lee Do-Hun, Lee Yong-Gyun, Hahn Jung-Tai: Simple synthesis of quinolines and dibenzo[b,f][1,5]diazocines under microwave irradiation. Tetrahetron Lett 2009, 50, 5805. <http://dx.doi.org/10.1016/j.tetlet.2009.07.150>
• Schmink Jason R., Leadbeater Nicholas E.: Probing “microwave effects” using Raman spectroscopy. Org Biomol Chem 2009, 7, 3842. <http://dx.doi.org/10.1039/b910591c>
• Efimova Yu. A., Artamonova T. V., Koldobskii G. I.: Tetrazoles: LIV. Alkylation of 5-aryltetrazoles under microwave activation. Russ J Org Chem 2009, 45, 725. <http://dx.doi.org/10.1134/S1070428009050133>
• Yadav Ganapati D, Sajgure Ashwini D, Dhoot Shrikant B: Insight into microwave irradiation and enzyme catalysis in enantioselective resolution of RS‐( ± )‐methyl mandelate. J Chem Technol Biotechnol 2008, 83, 1145. <http://dx.doi.org/10.1002/jctb.1975>
• Oliver Kappe C.: Microwave dielectric heating in synthetic organic chemistry. Chem Soc Rev 2008, 37, 1127. <http://dx.doi.org/10.1039/b803001b>
• Horikoshi Satoshi, Tsuzuki Junichi, Kajitani Masatsugu, Abe Masahiko, Serpone Nick: Microwave-enhanced radical reactions at ambient temperature : Part 3: Highly selective radical synthesis of 3-cyclohexyl-1-phenyl-1-butanone in a microwave double cylindrical cooled reactor. New J Chem 2008, 32, 2257. <http://dx.doi.org/10.1039/b810142f>
• Dandia Anshu, Singh Ruby, Sharma Rekha, Singh Dharmendra: Investigation of the Reaction of Chloroacetyl Chloride with 1,5-Benzothiazepines: Selective Synthesis of Azeto[2,1-d][1,5]benzothiazepines by Green Chemical Methods and Their Biological Activity. Phosphorus Sulfur Silicon Relat Elem 2008, 183, 3116. <http://dx.doi.org/10.1080/10426500802062236>
• Yadav Ganapati D, Sajgure Ashwini D: Synergism of microwave irradiation and enzyme catalysis in synthesis of isoniazid. J Chem Technol Biotechnol 2007, 82, 964. <http://dx.doi.org/10.1002/jctb.1738>
• Bezdushna Ella, Ritter Helmut: Microwave-Assisted Esterification of Methacrylic Acid and Polymer-Analogous Esterification of Poly[ethylene-co-(acrylic acid)] with Dissimilar Phenols. Macromol Rapid Commun 2007, 28, 443. <http://dx.doi.org/10.1002/marc.200600716>
• Toukoniitty Blanka, Roche Oriane, Mikkola Jyri-Pekka, Toukoniitty Esa, Klingstedt Fredrik, Eränen Kari, Salmi Tapio, Murzin Dmitry Yu.: Ethyl pyruvate hydrogenation under microwave irradiation. Chem Eng J 2007, 126, 103. <http://dx.doi.org/10.1016/j.cej.2006.09.016>
• Beldi M., Medimagh R., Chatti S., Marque S., Prim D., Loupy A., Delolme F.: Characterization of cyclic and non-cyclic poly-(ether-urethane)s bio-based sugar diols by a combination of MALDI-TOF and NMR. Euro Poly J 2007, 43, 3415. <http://dx.doi.org/10.1016/j.eurpolymj.2007.06.003>
• Mabrour Mahmoud, Bougrin Khalid, Benhida Rachid, Loupy André, Soufiaoui Mohamed: An efficient one-step regiospecific synthesis of novel isoxazolines and isoxazoles of N-substituted saccharin derivatives through solvent-free microwave-assisted [3+2] cycloaddition. Tetrahetron Lett 2007, 48, 443. <http://dx.doi.org/10.1016/j.tetlet.2006.11.067>
• Lee Dong Hwan, Park Sang-Eon, Cho Kyuho, Kim Younsoo, Athar Taimur, Lee Ik-Mo: Highly efficient microwave-accelerated preparation of β-ketoimines. Tetrahetron Lett 2007, 48, 8281. <http://dx.doi.org/10.1016/j.tetlet.2007.09.143>
• Gopalakrishnan M., Sureshkumar P., Kanagarajan V., Thanusu J.: New environmentally-friendly solvent-free synthesis of imines using calcium oxide under microwave irradiation. Res. Chem. Intermed. 2007, 33, 541. <http://dx.doi.org/10.1163/156856707782565822>
• Barluenga José, Fernández-Rodríguez Manuel A., García-García Patricia, Aguilar Enrique, Merino Isabel: Synthesis of Donor-Acceptor Alkynylcyclopropanes by Diastereoselective Cyclopropanation of Electron-Deficient Alkenes with Alkoxyalkynyl Fischer Carbene Complexes. Chem Eur J 2006, 12, 303. <http://dx.doi.org/10.1002/chem.200500918>
• Kamble Ravindra R., SUDHA Belagur S.: A Rapid and Convenient Synthetic Route to Novel 1,5-Benzodiazepine Derivatives of 5-Methyl-3-phenyl-2-oxo-Δ4-1,3,4-oxadiazolines fromp-Acetylphenylsydnone and Their Pharmacological Activity. Chin J Chem 2006, 24, 79. <http://dx.doi.org/10.1002/cjoc.200690025>
• Chaudhuri Mihir K., Hussain Sahid: An efficient synthesis of quinolines under solvent-free conditions. J Chem Sci 2006, 118, 199. <http://dx.doi.org/10.1007/BF02708474>
• Safaei-Ghomi J., Bamoniri A. H., Soltanian-Telkabadi M.: A modified and convenient method for the preparation of N-phenylpyrazoline derivatives. Chem Heterocycl Compd 2006, 42, 892. <http://dx.doi.org/10.1007/s10593-006-0176-1>
• Desai Krunal G., Desai Kishor R.: Green route for the heterocyclization of 2-mercaptobenzimidazole into β-lactum segment derivatives containing –CONH– bridge with benzimidazole: Screening in vitro antimicrobial activity with various microorganisms. biorg med chem 2006, 14, 8271. <http://dx.doi.org/10.1016/j.bmc.2006.09.017>
• Yadav Ganapati D., Desai Neesha M.: Novelties of low energy microwave irradiation in tri-phase vis-à-vis bi-liquid phase-transfer catalysis in selective etherification of aromatic phenols. Catal Commun 2006, 7, 325. <http://dx.doi.org/10.1016/j.catcom.2005.11.019>
• Chatti S., Bortolussi M., Bogdal D., Blais J.C., Loupy A.: Synthesis and properties of new poly(ether–ester)s containing aliphatic diol based on isosorbide. Effects of the microwave-assisted polycondensation. Euro Poly J 2006, 42, 410. <http://dx.doi.org/10.1016/j.eurpolymj.2005.08.009>
• Marquez Heiddy, Loupy André, Calderon Osmar, Pérez Eduardo R.: An eco-friendly protocol for synthesis of thiourea derivatives: 1-benzoyl-3-benzylguanidine and 1-benzoyl-3-benzyl-O-ethylisourea. A possible non-purely thermal microwave assisted reaction. Tetrahedron 2006, 62, 2616. <http://dx.doi.org/10.1016/j.tet.2005.12.037>
• Bogdal Dariusz, Bednarz Szczepan, Lukasiewicz Marcin: Microwave induced thermal gradients in solventless reaction systems. Tetrahedron 2006, 62, 9440. <http://dx.doi.org/10.1016/j.tet.2006.07.038>
• Pchelka Beata K., Loupy Andre, Petit Alain: Improvement and simplification of synthesis of 3-aryloxy-1,2-epoxypropanes using solvent-free conditions and microwave irradiations. Relation with medium effects and reaction mechanism. Tetrahedron 2006, 62, 10968. <http://dx.doi.org/10.1016/j.tet.2006.08.067>
• Mishra Jitendra Kumar, Srinivasa Rao J., Narahari Sastry G., Panda Gautam: Regioselective aminoethylation of 1,4-benzodiazepin-2-one under conventional heating and microwave irradiation. Tetrahetron Lett 2006, 47, 3357. <http://dx.doi.org/10.1016/j.tetlet.2006.03.094>
• Lebouvier Nicolas, Giraud Francis, Corbin Typhanie, Na Young Min, Le Baut Guillaume, Marchand Pascal, Le Borgne Marc: Efficient microwave-assisted synthesis of 1-(1H-indol-1-yl)-2-phenyl-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents. Tetrahetron Lett 2006, 47, 6479. <http://dx.doi.org/10.1016/j.tetlet.2006.03.199>
• Desai Krunal G., Desai Kishor R.: A facile microwave enhanced synthesis of sulfur-containing 5-membered heterocycles derived from 2-mercaptobenzothiazole over ZnCl ₂/DMF and antimicrobial activity evaluation. J of Sulfur Chem 2006, 27, 315. <http://dx.doi.org/10.1080/17415990600786409>
• Salehi Hojatollah, Guo Qing-Xiang: Efficient Magnesium Bromide-Catalyzed One-pot Synthesis of Substituted 1,2,3,4-Tetrahydropyrimidin-2-ones Under Solvent-free Conditions. Chin J Chem 2005, 23, 91. <http://dx.doi.org/10.1002/cjoc.200590021>
• Iannelli Mauro, Ritter Helmut: Microwave-Assisted Direct Synthesis and Polymerization of Chiral Acrylamide. Macromol Chem Phys 2005, 206, 349. <http://dx.doi.org/10.1002/macp.200400422>
• Zinck Philippe, Barbier-Baudry Denise, Loupy André: The Mechanism of Diene Polymerisation by Organolanthanide Catalysts Deduced from Microwave Experiments. Macromol Rapid Commun 2005, 26, 46. <http://dx.doi.org/10.1002/marc.200400434>
• Bezdushna Ella, Ritter Helmut, Troev Kolio: Microwave-Assisted Single-Step Synthesis of Poly(alkylene hydrogen phosphonate)s by Transesterification of Dimethyl Hydrogen Phosphonate with Poly(ethylene glycol). Macromol Rapid Commun 2005, 26, 471. <http://dx.doi.org/10.1002/marc.200400494>
• Bezdushna Ella, Ritter Helmut: Microwave Accelerated Synthesis ofN-Phenylmaleimide in a Single Step and Polymerization in Bulk. Macromol Rapid Commun 2005, 26, 1087. <http://dx.doi.org/10.1002/marc.200500070>
• Kuznetsov D. V., Raev V. A., Kuranov G. L., Arapov O. V., Kostikov R. R.: Microwave Activation in Organic Synthesis. Russ J Org Chem 2005, 41, 1719. <http://dx.doi.org/10.1007/s11178-006-0030-z>
• Bougrin K., Loupy A., Soufiaoui M.: Microwave-assisted solvent-free heterocyclic synthesis. J Photochem Photobiol C Photochem Rev 2005, 6, 139. <http://dx.doi.org/10.1016/j.jphotochemrev.2005.07.001>
• Iannelli Mauro, Alupei Valentina, Ritter Helmut: Selective microwave-accelerated synthesis and polymerization of chiral methacrylamide directly from methacrylic acid and (R)-1-phenyl-ethylamine. Tetrahedron 2005, 61, 1509. <http://dx.doi.org/10.1016/j.tet.2004.11.068>
• Chatti S., Bortolussi M., Bogdal D., Blais J.C., Loupy A.: Microwave-assisted polycondensation of aliphatic diols of isosorbide with aliphatic disulphonylesters via phase-transfer catalysis. Euro Poly J 2004, 40, 561. <http://dx.doi.org/10.1016/j.eurpolymj.2003.10.027>
• Torres Gerardo, Torres Wildeliz, Prieto José A.: Microwave-assisted epoxidation of hindered homoallylic alcohols using VO(acac)2: application to polypropionate synthesis. Tetrahedron 2004, 60, 10245. <http://dx.doi.org/10.1016/j.tet.2004.08.095>
• Nguyen Hoang‐Phuong, Znifeche Samira, Baboulène Michel: An Improved Greener Esterification of Fatty Alcohols Using a Renewable Acid–Ionic Liquid Couple as Catalyst–Solvent. Synth Common 2004, 34, 2085. <http://dx.doi.org/10.1081/SCC-120037923>
• Yadav Ganapati D., Bisht Priyal M.: Synergism of Low Energy Microwave Irradiation and Solid–Liquid Phase Transfer Catalysis for Selective Alkylation of Phenols to Phenolic Ethers. Synth Common 2004, 34, 2885. <http://dx.doi.org/10.1081/SCC-200026623>
• Cvengros Ján, Toma Stefan, Marque Sylvain, Loupy André: Synthesis of phosphonium salts under microwave activation — Leaving group and phosphine substituents effects. Can J Chem 2004, 82, 1365. <http://dx.doi.org/10.1139/v04-103>
• Chatti S., Bortolussi M., Loupy A., Blais J. C., Bogdal D., Roger P.: Synthesis of new polyethers derived from isoidide under phase-transfer catalysis: Reactivity and selectivity under microwaves and classical heating. J Appl Polym Sci 2003, 90, 1255. <http://dx.doi.org/10.1002/app.12719>
• Pérez Eduardo R, Loupy André, Liagre Marion, de Guzzi Plepis Ana M, Cordeiro Paulo J: Clean and efficient microwave-solvent-free synthesis of 1-(2′,4′-dichlorophenacyl) azoles. Tetrahedron 2003, 59, 865. <http://dx.doi.org/10.1016/S0040-4020(02)01622-8>
• Song Suk Jin, Cho Seong Jin, Park Dong Kyu, Kwon Tae Woo, Jenekhe Samson A.: Microwave enhanced solvent-free synthesis of a library of quinoline derivatives. Tetrahetron Lett 2003, 44, 255. <http://dx.doi.org/10.1016/S0040-4039(02)02499-1>
• Chauhan S. M. S., Singh Ram, Geetanjali: Microwave-Assisted Synthesis of 10-Substituted Isoalloxazines in the Presence of Solid Acids. Synth Common 2003, 33, 1179. <http://dx.doi.org/10.1081/SCC-120017194>
• Chaouchi Mehdi, Loupy André, Marque Sylvain, Petit Alain: Solvent-Free Microwave-Assisted Aromatic Nucleophilic Substitution − Synthesis of Aromatic Ethers. Eur J Org Chem 2002, 2002, 1278. <http://dx.doi.org/10.1002/1099-0690(200204)2002:7<1278::AID-EJOC1278>3.0.CO;2-B>
• Chatti S., Bortolussi M., Loupy A., Blais J.C., Bogdal D., Majdoub M.: Efficient synthesis of polyethers from isosorbide by microwave-assisted phase transfer catalysis. Euro Poly J 2002, 38, 1851. <http://dx.doi.org/10.1016/S0014-3057(02)00071-X>
• Perreux Laurence, Loupy André, Volatron François: Solvent-free preparation of amides from acids and primary amines under microwave irradiation. Tetrahedron 2002, 58, 2155. <http://dx.doi.org/10.1016/S0040-4020(02)00085-6>
• Perreux Laurence, Loupy André: A tentative rationalization of microwave effects in organic synthesis according to the reaction medium, and mechanistic considerations. Tetrahedron 2001, 57, 9199. <http://dx.doi.org/10.1016/S0040-4020(01)00905-X>