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1
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For other examples of fluorous mixture syntheses, see: (a) Luo, Z.; Zhang, Q.; Oderaotoshi, Y.; Curran, D. P. Science 2001, 291, 1766-1769.
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(d) Dandapani, S.; Jeske, M.; Curran, D. P. Proc. Nat. Acad. Sci. U.S.A. 2004, 101, 12008-12012.
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(e) Short review: Zhang, W. Arkivoc 2004, 101-109.
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Zhang, W.1
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3943111078
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Gladysz, J. A., Curran, D. P., Horvath, I., Eds.; Wiley-VCH: Weinheim
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(b) Curran, D. P. In Handbook of Fluorous Chemistry; Gladysz, J. A., Curran, D. P., Horvath, I., Eds.; Wiley-VCH: Weinheim, 2004; pp 101-128.
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Curran, D.P.1
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4444355871
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(a) Böhm, H.-J.; Banner, D.; Bendals, S.; Kansey, M.; Kuhn, K.; Müller, K.; Obst-Sander, U.; Stahl, M. ChemBioChem 2004, 5, 637-643.
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Bendals, S.3
Kansey, M.4
Kuhn, K.5
Müller, K.6
Obst-Sander, U.7
Stahl, M.8
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4544316921
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(b) Biffinger, J. C.; Kim, H. W.; DiMagno, S. G. ChemBioChem 2004, 5, 622-627.
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ChemBioChem
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Biffinger, J.C.1
Kim, H.W.2
Dimagno, S.G.3
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10
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4544353451
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(c) Ojima, I. ChemBioChem 2004, 5, 628-635. This issue of ChemBioChem also contains other articles and reviews regarding fluorine in the life sciences.
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ChemBioChem
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Ojima, I.1
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12
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13544273419
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Manku, S.; Curran, D. P. J. Comb. Chem. 2005, 7, 63-68. In this work, secondary propargyl esters [RCOOCH(Me)C≡CTMS] were studied.
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Manku, S.1
Curran, D.P.2
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(a) Curran, D. P.; Amatore, M.; Guthrie, D.; Campbell, M.; Go, E.; Luo, Z. J. Org. Chem., 2003, 68, 4643-4647.
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Luo, Z.6
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14
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19544372121
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(b) The fluorous reagents and columns were purchased from Fluorous Technologies, Inc. (www.fluorous.com).
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15
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19544383258
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note
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(c) DPC holds an equity interest in this company.
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16
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0141854273
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For another example of fluorous synthesis of hydantoins, see: Zhang, W.; Lu, Y. Org. Lett. 2003, 5, 2555-2558.
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Org. Lett.
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Lu, Y.2
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For a review on the use of fluorous reagents for the synthesis of heterocycles, see: Zhang, W. Chem. Rev. 2004, 104, 2531-2556.
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Zhang, W.1
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For the use of Rh(I) catalysts on alkynyl allenes, see: (a) Brummond, K. M.; Mitasev, B. Org. Lett. 2004, 6, 2245-2248.
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Mitasev, B.2
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(c) Brummond, K. M.; Chen, H.; Sill, P.; You, L. J. Am. Chem. Soc. 2002, 124, 15186-15187.
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22
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19544373652
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note
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Trimethylsilylpropargyl alcohol, which was used in the initial tag assignments, failed to undergo the ester-enolate Claisen rearrangement cleanly.
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-
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24
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19544368499
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note
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1 = Me) gave a 4/1 mixture of 10-syn/10-anti with little or no 11. Full details can be found in Supporting Information.
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25
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0038260112
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Zhang, W. Org. Lett. 2003, 5, 1011-1013.
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Zhang, W.1
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