Pure and Applied Chemistry

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• Acevedo Orlando, Jorgensen Wiliiam L.: Quantum and molecular mechanical Monte Carlo techniques for modeling condensed-phase reactions. WIREs Comput Mol Sci 2014, n/a. <http://dx.doi.org/10.1002/wcms.1180>
• Manna Arpan, Kumar Anil: Why Does Water Accelerate Organic Reactions under Heterogeneous Condition?. J. Phys. Chem. A 2013, 117, 2446. <http://dx.doi.org/10.1021/jp4002934>
• Yang Xin, Xue Ying: QM/MM investigation on 1,3-dipolar cycloadditions of the phthalazinium dicyanomethanide with three different dipolarophiles on water and in solution. Phys. Chem. Chem. Phys. 2013, 15, 11846. <http://dx.doi.org/10.1039/c3cp51048d>
• Sela Tal, Vigalok Arkadi: Salt-Controlled Selectivity in “on Water” and “in Water” Passerini-Type Multicomponent Reactions. Adv. Synth. Catal. 2012, 354, 2407. <http://dx.doi.org/10.1002/adsc.201200448>
• Javan Marjan Jebeli, Tehrani Zahra Aliakbar, Fattahi Alireza, Hashemi Mohammad Mahmoodi: How hydrogen-bonded MnO4 - can influence oxidation of olefins in both gas phase and solution?. J. Phys. Org. Chem. 2012, 25, 1198. <http://dx.doi.org/10.1002/poc.2992>
• Tan Huaping, Rubin J. Peter, Marra Kacey G.: Direct Synthesis of Biodegradable Polysaccharide Derivative Hydrogels Through Aqueous Diels-Alder Chemistry. Macromol Rapid Commun 2011, 32, 905. <http://dx.doi.org/10.1002/marc.201100125>
• Benchouk W., Mekelleche S. M., Silvi B., Aurell M. J., Domingo L. R.: Understanding the kinetic solvent effects on the 1,3-dipolar cycloaddition of benzonitrile N-oxide: a DFT study. J Phys Org Chem 2011, 24, 611. <http://dx.doi.org/10.1002/poc.1858>
• Paul Nidhin, Muthusubramanian Shanmugam, Bhuvanesh Nattamai: A green protocol for the synthesis of conformationally rigid sulfur linked bisquinolines by double Friedlander reaction in water. NJC 2011, 35, 2607. <http://dx.doi.org/10.1039/c1nj20539k>
• El-Mallah N. M., Senior S. A., Nabil G. M., Ramadan M. Sh., Hamed E. A.: Effect of acetonitrile-water mixtures on the reaction of dinitrochlorobenzene and dinitrochlorobenzotrifluoride with hydroxide ion. Int J Chem Kinet 2010, 42, 453. <http://dx.doi.org/10.1002/kin.20495>
• Engberts Jan B. F. N., Feringa Ben L., Keller Erik, Otto Sijbren: Lewis-acid catalysis of carbon carbon bond forming reactions in water. Recl Trav Chim Pays-Bas 2010, 115, 457. <http://dx.doi.org/10.1002/recl.19961151103>
• Janus Ewa, Bittner Bożena: Triethylsulfonium Bistriflimide as the Reaction Medium in Catalyzed and Uncatalyzed Cycloaddition [4 + 2]. Catal Lett 2010, 134, 147. <http://dx.doi.org/10.1007/s10562-009-0211-9>
• Tirado-Rives Julian, Jorgensen William L., Thomas Laura L.: Quantum Mechanical/Molecular Mechanical Modeling Finds Diels−Alder Reactions Are Accelerated Less on the Surface of Water Than in Water. J Am Chem Soc 2010, 132, 3097. <http://dx.doi.org/10.1021/ja909740y>
• Shapiro Nelly, Kramer Maria, Goldberg Israel, Vigalok Arkadi: Straightforward radical organic chemistry in neat conditions and “on water”. Green Chem 2010, 12, 582. <http://dx.doi.org/10.1039/b922475k>
• Rueping Magnus, Theissmann Thomas: Asymmetric Brønsted acid catalysis in aqueous solution. Chem Sci 2010, 1, 473. <http://dx.doi.org/10.1039/c0sc00206b>
• Jung Yousung, Marcus R A: Protruding interfacial OH groups and ‘on-water’ heterogeneous catalysis. J Phys Condens Matter 2010, 22, 284117. <http://dx.doi.org/10.1088/0953-8984/22/28/284117>
• Shi Meng, Lu Jiao, Shoichet Molly S.: Organic nanoscale drug carriers coupled with ligands for targeted drug delivery in cancer. J Mater Chem 2009, 19, 5485. <http://dx.doi.org/10.1039/b822319j>
• Coutouli-Argyropoulou Evdoxia, Sarridis Prodromos, Gkizis Petros: Water as the medium of choice for the 1,3-dipolar cycloaddition reactions of hydrophobic nitrones. Green Chem 2009, 11, 1906. <http://dx.doi.org/10.1039/b916765j>
• Wu Xiaofeng, Liu Jianke, Di Tommaso Devis, Iggo Jonathan A., Catlow C. Richard A., Bacsa John, Xiao Jianliang: A Multilateral Mechanistic Study into Asymmetric Transfer Hydrogenation in Water . Chem Eur J 2008, 14, 7699. <http://dx.doi.org/10.1002/chem.200800559>
• Steven Victoria, Graham Duncan: Oligonucleotide conjugation to a cell-penetrating (TAT) peptide by Diels–Alder cycloaddition. Org Biomol Chem 2008, 6, 3781. <http://dx.doi.org/10.1039/b807843b>
• López Ignacio, Silvero Guadalupe, Arévalo María José, Babiano Reyes, Palacios Juan Carlos, Bravo José Luis: Enhanced Diels–Alder reactions: on the role of mineral catalysts and microwave irradiation in ionic liquids as recyclable media. Tetrahedron 2007, 63, 2901. <http://dx.doi.org/10.1016/j.tet.2007.01.031>
• Butler Richard N., Coyne Anthony G., Moloney Eamon M.: Organic synthesis in water: 1,3-dipolar cycloaddition reactions at ambient temperature with aqueous suspensions of solid reactants. Tetrahetron Lett 2007, 48, 3501. <http://dx.doi.org/10.1016/j.tetlet.2007.03.119>
• Kleiner Christian M., Schreiner Peter R.: Hydrophobic amplification of noncovalent organocatalysis. Chem Commun 2006, 4315. <http://dx.doi.org/10.1039/b605850g>
• Butler Richard N., Coyne Anthony G., Cunningham William J., Moloney Eamon M., Burke Luke A.: Water and theHuisgen Cycloaddition Reaction: A Focus on Polar Contributions to the Transition State in the Reactions of Dicyano(phthalazinium)methanide with Substituted Styrenes and Benzylidene Acetones. HCA 2005, 88, 1611. <http://dx.doi.org/10.1002/hlca.200590128>
• Mahindaratne Mathew P.D., Quiñones Brian A., Recio Antonio, Rodriguez Eric A., Lakner Frederick J., Negrete George R.: Salt, concentration, and temperature effects on an asparagine-based, aqueous Diels–Alder cycloaddition. Tetrahedron 2005, 61, 9495. <http://dx.doi.org/10.1016/j.tet.2005.08.003>
• Leininger Neil F., Gainer John L., Kirwan Donald J.: Effect of aqueous PEG or PPG solvents on reaction selectivity and Gibbs energies. AIChE 2004, 50, 511. <http://dx.doi.org/10.1002/aic.10044>
• Chen I-Hon, Young Jun-Nan, Yu Shuchun Joyce: Recyclable organotungsten Lewis acid and microwave assisted Diels–Alder reactions in water and in ionic liquids. Tetrahedron 2004, 60, 11903. <http://dx.doi.org/10.1016/j.tet.2004.09.078>
• A Model for Correlation of Various Solvatochromic Parameters with Composition in Aqueous and Organic Binary Solvent Systems. Bulletin of the Korean Chemical Society 2004, 25, 1165. <http://dx.doi.org/10.5012/bkcs.2004.25.8.1165>
• Itami Kenichiro, Yoshida Jun-Ichi: The Use of Hydrophilic Groups in Aqueous Organic Reactions. Chem Record 2002, 2, 213. <http://dx.doi.org/10.1002/tcr.10021>
• Fringuelli Francesco, Piermatti Oriana, Pizzo Ferdinando, Vaccaro Luigi: Recent Advances in Lewis Acid Catalyzed Diels−Alder Reactions in Aqueous Media. Eur J Org Chem 2001, 2001, 439. <http://dx.doi.org/10.1002/1099-0690(200102)2001:3<439::AID-EJOC439>3.0.CO;2-B>
• Yangjeh A. Habibi, Gholami M. R., Mostaghim R.: Dual-parameter correlations on rate of dehydration step of a condensation reaction in aqueous solutions of ethanol, propan-2-ol and 2-methylpropan-2-ol. J Phys Org Chem 2001, 14, 884. <http://dx.doi.org/10.1002/poc.438>
• Gholami M. R., Yangjeh A. Habibi: Multiparameter correlation of the rate of a [2 + 2] cycloaddition reaction versus solvophobicity parameter and normalized polarity parameter in aqueous solutions. J Phys Org Chem 2000, 13, 468. <http://dx.doi.org/10.1002/1099-1395(200008)13:8<468::AID-POC258>3.0.CO;2-E>
• Aramini Andrea, Brinchi Lucia, Germani Raimondo, Savelli Gianfranco: Reductions of α,β-Unsaturated Ketones by NaBH4 or NaBH4 + CoCl2: Selectivity Control by Water or by Aqueous Micellar Solutions. Eur J Org Chem 2000, 2000, 1793. <http://dx.doi.org/10.1002/(SICI)1099-0690(200005)2000:9<1793::AID-EJOC1793>3.0.CO;2-A>
• Kitazume Tomoya: Green chemistry development in fluorine science. J FLUORINE CHEM 2000, 105, 265. <http://dx.doi.org/10.1016/S0022-1139(99)00269-9>
• Melekhov Alex, Forgione Pat, Legoupy Stéphanie, Fallis Alex G.: Tether-Controlled Cycloadditions for the Asymmetric Synthesis of Decalins:  Increased Selectivity in Acetonitrile Solvent. Org Lett 2000, 2, 2793. <http://dx.doi.org/10.1021/ol0062042>
• Jaeger David A., Su Dan: Regioselectivity control in a Diels-Alder reaction of a surfactant 1,3-diene with a surfactant dienophile. Tetrahetron Lett 1999, 40, 257. <http://dx.doi.org/10.1016/S0040-4039(98)02350-8>
• Su Dan, Jaeger David A.: High regioselectivity in the Diels-Alder reaction of a surfactant 1,3-diene with a surfactant dienophile resulting from a short tether between their functional groups and head groups. Tetrahetron Lett 1999, 40, 7871. <http://dx.doi.org/10.1016/S0040-4039(99)01637-8>
• Rohr Uwe, Schatz Jürgen, Sauer Jürgen: Thio- and Selenocarbonyl Compounds as “Superdienophiles” in [4+2] Cycloadditions. Eur J Org Chem 1998, 1998, 2875. <http://dx.doi.org/10.1002/(SICI)1099-0690(199812)1998:12<2875::AID-EJOC2875>3.0.CO;2-N>
• Brinchi Lucia, Di Profio Pietro, Germani Raimondo, Savelli Gianfranco, Bunton Clifford A.: Chemoselectivity in SN2-E2 reactions induced by aqueous association colloids. Colloid Surf A Phys Eng Aspects 1998, 132, 303. <http://dx.doi.org/10.1016/S0927-7757(97)00161-1>
• P. Repasky Matthew, L. Jorgensen William: Ab initio and Monte Carlo study of solvent eÜects on a 1,3–dipolar cycloaddition. Faraday Disc 1998, 110, 379. <http://dx.doi.org/10.1039/a802427h>
• Sauer Jürgen, Schuhbauer Hans Markus: Solvent Effects in [4+2] Cycloadditions of Polyhalogenated Cyclopentadienes with 4-Phenyl-1,2,4-triazoline-3,5-dione. Liebigs Ann /Recueil 1997, 1997, 1739. <http://dx.doi.org/10.1002/jlac.199719970816>
• Kuznetsova T. G., Ione K. G., Testova N. V., Salakhutdinov N. F.: Diene condensation on zeolites, II. Influence of the zeolite structure and the nature of substituting cation on the reaction of alloocimene with α-methacrolein. React Kinet Catal Lett 1997, 62, 287. <http://dx.doi.org/10.1007/BF02475465>