Mg(OTf)₂ + ionic liquid - recyclable catalytic system in diels-alder reaction

Tarasow, T. M. & Eaton, B. E. (1999) The Diels-Alder reaction and biopolymer catalysis, Cellular and Molecular Life Sciences, 55, 1463-1472. doi: 1420-682X:99:111463-10.Search in Google Scholar

Ilker M. F. & Schuke H., Coughlin E. B. Modular norbornene derivatives for the preparation of well-defined amphiphilic polymers: Study of the lipid membrane disruption activities. Macromolecules, 37(3), 694-700. doi: 10.1021/ma035407d.10.1021/ma035407dSearch in Google Scholar

Willson, C. G., Okoroanyanwu, U. & Medieros, D. (2000). US Patent No. 6103445-Photoresist compositions comprising norbornene derivative polymers with acid labile groups.Search in Google Scholar

Diels O. & Alder K. (1931) Synthesen in der hydroaromatischen Reihe; XII. Mitteilung. "Dien-Synthesen" sauerstoffhaltiger Heteroringe.2. Dien-Synthesen des Furans. Ann. Chem. 490, 243-257.Search in Google Scholar

Pocker Y. & Ellsworth, D. L., (1977). Electrostatic Catalysis by Ionic Aggregates. 4. Rearrangement of 1 -Phenylallyl Chloride in Lithium Perchlorate Solutions in Aprotic Solvents. J. Am. Chem. Soc. 99, 2276-2284. doi: 10.1021/ja00449a042.10.1021/ja00449a042Search in Google Scholar

Weinstein, R. D., Renslo, A. R., Danheiser, R. L., Harris, J. G. & Tester, J. W. (1996). Kinetic Correlation of Diels-Alder Reactions in Supercritical Carbon Dioxide. J. Phys. Chem. 100, 12337-12341. doi: 10.1021/jp960180.Search in Google Scholar

Fringuelli, F. & Tachici, A. (2002). Wiley. The Diels-Alder reaction: selected practical methods. (pp. 251-278).Search in Google Scholar

Silvero, G., Arevalo, M. J., Bravo, J. L., Avalos, M., Jimenez, J. L. & Lopez, I. (2005) An in-depth look at the effect of Lewis acid catalysts on Diels-Alder cycloadditions in ionic liquids. Tetrahedron, 61, 7105-7111. doi:10.1016/j.tet.2005.05.06410.1016/j.tet.2005.05.064Search in Google Scholar

Kobayashi, S., Hachiya, I., Araki, M. & Ishitani, H., (1993) 4,4'-di-tert-butylbiphenyl-catalysed lithiation of 2,3-dichloropropene: A Barbier-type practical alternative to 2,3-dilithiopropene. Tetrahedron Letters, 34, 1755-3758. doi:10.1016/S0040-4039(00)91989-0.10.1016/S0040-4039(00)91989-0Search in Google Scholar

Otto, G., Boccaletti, J. B. & Engberts, F. N., (1998) A Chiral Lewis-Acid-Catalyzed Diels-Alder Reaction. Water-Enhanced Enantioselectivity. J. Am. Chem. Soc. 120, 4238-4239. doi: 10.1021/ja972772+.10.1021/ja972772+Search in Google Scholar

Kumar, A. & Pawar, S. S. (2004) Converting exo-Selective Diels-Alder Reaction to endo-Selective in Chloroloaluminate Ionic Liquids. J. Org. Chem. 69, 1419-1420. doi: 10.1021/jo035038j.10.1021/jo035038j14961709Search in Google Scholar

Yin, D., Li, C., Li, B., Tao, L. & Yin, D., (2005) High Regioselective Diels-Alder Reaction of Myrcene with Acrolein Catalyzed by Zinc-Containing Ionic Liquids. Adv. Synth. Catal. 347, 137-142. doi: 10.1002/adsc.200404233.10.1002/adsc.200404233Search in Google Scholar

Lopez, I., Silvero, G., Arevalo, M. J., Babiano, R., Palacios, J. C. & Bravo, J. L. (2007). Enhanced Diels-Alder reactions: on the role of mineral catalysts and microwave irradiation in ionic liquids as recyclable media. Tetrahedron, 63, 2901-2906. doi:10.1016/j.tet.2007.01.031.10.1016/j.tet.2007.01.031Search in Google Scholar

Sarma, D. & Kumar, A., (2008) Rare earth metal triflates promoted Diels-Alder reactions in ionic liquids. Appl. Catal. A: Gen. 335, 1-6. doi:10.1016/j.apcata.2007.10.026.10.1016/j.apcata.2007.10.026Search in Google Scholar

Bortolini, O. D., Nino, A., Garofalo, A., Maiuolo, L., Procopio, A. & Russo B. (2010) Erbium triflate in ionic liquids: A recyclable system of improving selectivity in Diels-Alder reactions. Appl. Catalysis A: General, 372, 124-129. doi:10.1016/j.apcata.2009.10.020.10.1016/j.apcata.2009.10.020Search in Google Scholar

Song, Ch. E., Shim, W. H., Roh, E. J., Lee, S., Choi, J. H., (2001) Ionic liquids as powerful media in scandium triflate catalysed Diels-Alder reactions: significant rate acceleration, selectivity improvement and easy recycling of catalyst Chem. Commun., 1122-1123. doi: 10.1039/b101140p.10.1039/b101140pSearch in Google Scholar

Vidis, A., Kusters, E., Sedelmeier, G. & Dyson, P. J., (2008) Effect of Lewis acids on the Diels-Alder reaction in ionic liquids with different activation modes. J. Phys. Org. Chem. 21, 264-270. doi:10.1016/j.apcata.2009.10.020.10.1016/j.apcata.2009.10.020Search in Google Scholar

Ludley, P. & Karodia, N. (2001) Phosphonium tosylates as solvents for the Diels-Alder reaction. Tetrahedron Lett., 42, 2011-2014. doi:10.1016/S0040-4039(01)00064-810.1016/S0040-4039(01)00064-8Search in Google Scholar

Janus, E. & Bittner, B. (2010) Triethylsulfonium Bistriflimide as the Reaction Medium in Catalyzed and Uncatalyzed Cycloaddition [4 + 2]. Catalysis Lett. 134, (1-2), 147-154 doi:10.1007/s10562-009-0211-9.10.1007/s10562-009-0211-9Search in Google Scholar