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Introduction: Curran, D. P.; Hadida, S.; He, M. J. Org. Chem. 1997, 62, 6714-6715.
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Introduction: Curran, D. P.; Hadida, S.; He, M. J. Org. Chem. 1997, 62, 6714-6715.
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3
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84958612634
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Gladysz, J. A, Curran, D. P, Horvath, I. T, Eds, Wiley-VCH: Weinheim
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(b)Curran, D.P. In The Handbook of Fluorous Chemistry; Gladysz, J. A., Curran, D. P., Horvath, I. T., Eds.; Wiley-VCH: Weinheim, 2004; pp 101-127.
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In The Handbook of Fluorous Chemistry
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Curran, D.P.1
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6
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13244253108
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Gladysz, J. A, Curran, D. P, Horvath, I. T, Eds, Wiley-VCH: Weinheim
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(a) Gladysz, J. A.; Emnet, C. In The Handbook of Fluorous Chemistry; Gladysz, J. A., Curran, D. P., Horvath, I. T., Eds.; Wiley-VCH: Weinheim, 2004; pp 11-23.
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The Handbook of Fluorous Chemistry
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Gladysz, J.A.1
Emnet, C.2
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7
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(b) Ryu, I.; Matsubara, H.; Emnet, G.; Gladysz, J. A.; Takeuchi, S.; Nakamura, Y.; Curran, D. P. In Green Reaction Media in Organic Synthesis; Blackwell: Ames, IO, 2005; pp 59-124.
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Green Reaction Media in Organic Synthesis; Blackwell: Ames, IO
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Ryu, I.1
Matsubara, H.2
Emnet, G.3
Gladysz, J.A.4
Takeuchi, S.5
Nakamura, Y.6
Curran, D.P.7
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8
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Examples of applications of HFEs as reaction solvents: (a) Mizuno, M.; Goto, K.; Miura, T.; Matsuura, T.; Inazu, T. Tetrahedron Lett. 2004, 45, 3425-3428.
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Examples of applications of HFEs as reaction solvents: (a) Mizuno, M.; Goto, K.; Miura, T.; Matsuura, T.; Inazu, T. Tetrahedron Lett. 2004, 45, 3425-3428.
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(b) Fukuyama, T.; Arai, M.; Matsubara, H.; Ryu, I. J. Org. Chem. 2004, 69, 8105-8107.
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J. Org. Chem
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Arai, M.2
Matsubara, H.3
Ryu, I.4
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Examples of applications of HFEs as liquid-liquid extraction solvents: Yu, M. S.; Curran, D. P.; Nagashima, T. Org. Lett. 2005, 7, 3677-3680.
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Examples of applications of HFEs as liquid-liquid extraction solvents: Yu, M. S.; Curran, D. P.; Nagashima, T. Org. Lett. 2005, 7, 3677-3680.
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(b) Curran, D. P.; Bajpai, R.; Sanger, E. Adv. Synth. Catal. 2006, 348, 1621-1624.
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Adv. Synth. Catal
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Curran, D.P.1
Bajpai, R.2
Sanger, E.3
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35548930597
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HFE solvents are produced by 3M under the tradename Novec: http://www.3m.com/Product/information/Novec-Engineered-Fluid.html. Most solvents are mixtures of isomers. For example, HFE-7100 is a mixture of perfluorobutyl methyl ether and perfluoroisobutyl methyl ether (n- and isobutyl groups). HFE-7100 is also available from Sigma-Aldrich.
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(a) HFE solvents are produced by 3M under the tradename Novec: http://www.3m.com/Product/information/Novec-Engineered-Fluid.html. Most solvents are mixtures of isomers. For example, HFE-7100 is a mixture of perfluorobutyl methyl ether and perfluoroisobutyl methyl ether (n- and isobutyl groups). HFE-7100 is also available from Sigma-Aldrich.
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14
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35548950600
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DPC owns an equity interest in Fluorous Technologies, Inc
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(b) DPC owns an equity interest in Fluorous Technologies, Inc.
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15
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14844292360
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Neilson, A. H, Ed, Springer-Verlag: Berlin
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(a) Wallington, T. J.; Nielsen, O. J. In Handbook of Environmental Chemistry: Organofluorines; Neilson, A. H., Ed.; Springer-Verlag: Berlin, 2002; Vol. 3, pp 85-102.
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Wallington, T.J.1
Nielsen, O.J.2
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35548932333
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Most HFEs are not classified as a volatile organic compound (VOC) and are approved for use under the US EPA Significant New Alternatives Program (SNAP): http://www.epa.gov/ozone/snap/regulations.html.
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(b) Most HFEs are not classified as a volatile organic compound (VOC) and are approved for use under the US EPA Significant New Alternatives Program (SNAP): http://www.epa.gov/ozone/snap/regulations.html.
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17
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4544275536
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Goodman, M, Felix, A, Moroder, L, Toniolo, C, Eds, Thieme-Verlag: Stuttgart
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(a) Podlech, J. In Houben-Weyl Methods of Organic Chemistry. Synthesis of Peptides and Peptidomimetics; Goodman, M., Felix, A., Moroder, L., Toniolo, C., Eds.; Thieme-Verlag: Stuttgart, 2001; Vol. E22a, pp 517-533.
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Houben-Weyl Methods of Organic Chemistry. Synthesis of Peptides and Peptidomimetics
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Podlech, J.1
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(b) Reagents for Glycoside, Nucleotide, and Peptide Synthesis; Crich, D., Ed.; Wiley: New York, 2005.
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Reagents for Glycoside, Nucleotide, and Peptide Synthesis
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0348041985
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For examples, see: a
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For examples, see: (a) Sauer, D. R.; Kalvin, D.; Phelan, K. M. Org. Lett. 2003, 5,4721-4724.
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Org. Lett
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Sauer, D.R.1
Kalvin, D.2
Phelan, K.M.3
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(b) Lannuzel, M.; Lamothe, M.; Perez, M. Tetrahedron Lett. 2001, 42, 6703-6705.
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Tetrahedron Lett
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Lamothe, M.2
Perez, M.3
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(c) Jamieson, C.; Congreve, M. S.; Emiabata-Smith, D.; Ley, S. V. Synlett 2000, 1603-1607.
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Synlett
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Jamieson, C.1
Congreve, M.S.2
Emiabata-Smith, D.3
Ley, S.V.4
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(a) Palomo, C.; Aizpurua, J. M.; Loinaz, I.; Fernandez-Berridi, M. J.; Irusta, L. Org. Lett. 2001, 3, 2361-2364.
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Org. Lett
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Palomo, C.1
Aizpurua, J.M.2
Loinaz, I.3
Fernandez-Berridi, M.J.4
Irusta, L.5
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Gladysz, J. A, Curran, D. P, Horvath, I. T, Eds, Wiley-VCH: Weinheim
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(b) Aizpurua, J. M.; Palomo, G; Loinaz, I. In The Handbook of Fluorous Chemistry; Gladysz, J. A., Curran, D. P., Horvath, I. T., Eds.; Wiley-VCH: Weinheim, 2004; pp 459-461.
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Ph.D. Thesis, University of Pittsburgh, The thesis is archived and openly available from the University of Pittsburgh Library Electronic Thesis Deposition (ETD) site at
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Keller, A., Ph.D. Thesis, University of Pittsburgh, 2007. The thesis is archived and openly available from the University of Pittsburgh Library Electronic Thesis Deposition (ETD) site at http://etd.library.pitt.edu/ETD/ available/etd-04122007-142347/.
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Keller, A.1
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35548965889
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The fluorous urea can be recovered in about 80, after purification for reuse
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The fluorous urea can be recovered in about 80% (after purification) for reuse.
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26
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79957981525
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Hartke, K.; Rossbach, F. Angew. Chem., Int. Ed. 1968, 7, 72-74.
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Hartke, K.1
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