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U.S. Patent 5,-773,468, 1998
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Kim, S. C.; Son, Y. C.; Choi, H. I.; Yoon, H.; Park, C. H.; Choy, N.; Lee, C. S.; Koh, J. S.; Moon, K. Y.; Jung, W. H.; Kim, C. R. U.S. Patent 5,-773,468, 1998.
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Kim, S.C.1
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Lee, C.S.7
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0346210172
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Clark, J. H., Ed.; RSC Clean Technology Monographs; Royal Society of Chemistry: Cambridge, UK
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For a discussion on the safe use of hydrogen peroxide, see: Jones, C. W. In Applications of Hydrogen Peroxide and Derivatives; Clark, J. H., Ed.; RSC Clean Technology Monographs; Royal Society of Chemistry: Cambridge, UK, 1999; pp 21-35.
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Jones, C.W.1
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0030738769
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(b) For the epoxidation of a double bond, see: Rudolph, J.; Reddy, K. L. ; Chiang, J. P.; Sharpless, K. B. J. Am. Chem. Soc. 1997, 119, 6189.
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Rudolph, J.1
Reddy, K.L.2
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Sharpless, K.B.4
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0029783677
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Miyauchi, H.1
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Ohashi, N.3
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0036748282
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Chang, J. H.; Lee, K. W.; Nam, D. H.; Kim, W. S.; Shin, H. Org. Process Res. Dev. 2002, 6, 674.
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Chang, J.H.1
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0347471350
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(a) Corey, H. S., Jr.; McCormick, J. R. D.; Swensen, W. E. J. Am. Chem. Soc. 1964, 86, 1884.
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Corey Jr., H.S.1
McCormick, J.R.D.2
Swensen, W.E.3
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17
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0346210180
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note
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3) δ 8.39 (d, 1H, J = 4.1 Hz) 7.95 (d, 2H, J = 7.4 Hz), 7.85-7.65 (m, 15H), 7.55-7.42 (m, 2H), 5.08 (dd, 1H, J = 6.9, 5.5 Hz), 3.84-3.74 (m, 2H), 3.14-3.11 (m, 2H), 2.30 (m, 1H), 0.98 (d, 6H, J = 6.0 Hz). (Equation presented)
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18
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21344455641
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Lee, C. S.; Choy, N.; Son, Y. C.; Park, C.; Choi, H.; Moon, K. Y.; Jung, W. H.; Kim, S. C.; Yoon, H. Bull. Korean Chem. Soc. 1996, 17, 294.
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Bull. Korean Chem. Soc.
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Lee, C.S.1
Choy, N.2
Son, Y.C.3
Park, C.4
Choi, H.5
Moon, K.Y.6
Jung, W.H.7
Kim, S.C.8
Yoon, H.9
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20
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0348101332
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note
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cp = 73.4 Hz).
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21
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37049091874
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In general, triphenylphosphonium salt is transformed to diphenylphosphine oxide under reflux in strongly basic aqueous conditions, see: Buss, A. D.; Warren, S. J. Chem. Soc., Perkin Trans. 1 1985, 2307.
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(1985)
J. Chem. Soc., Perkin Trans. 1
, pp. 2307
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Buss, A.D.1
Warren, S.2
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24
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0001345433
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The observed selectivity is quite close to Roush's result on (Z)-allylic carbamate. Please refer to: Roush, W. R.; Straub, J. A.; Brown, R. J. J. Org. Chem. 1987, 52, 5127.
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(1987)
J. Org. Chem.
, vol.52
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Roush, W.R.1
Straub, J.A.2
Brown, R.J.3
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28
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0030271965
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Schultz, M.; Kluge, R.; Liebsch, S.; Lessig, J.; Halik, M.; Gadissa, F. Tetrahedron 1996, 52, 13151.
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Tetrahedron
, vol.52
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Schultz, M.1
Kluge, R.2
Liebsch, S.3
Lessig, J.4
Halik, M.5
Gadissa, F.6
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30
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0040321853
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For an excellent review on the directing effect of various groups in epoxidation, see: Dryuk, V. G.; Kartsev, V. G. Russ. Chem. Rev. 1999, 68, 183.
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Russ. Chem. Rev.
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Dryuk, V.G.1
Kartsev, V.G.2
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33
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84889491424
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Permaleic acid and trifluoroperacetic acid were prepared in situ by the addition of maleic anhydride or trifluoroacetic anhydride (TFAA), respectively to urea-hydrogen peroxide (UHP). The safety concern on the use of these reagents was discussed in detail in the reference. See: Cooper, M. S.; Heaney, H.; Newbold, A. J.; Sanderson, W. R. Synlett 1990, 533.
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(1990)
Synlett
, pp. 533
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Cooper, M.S.1
Heaney, H.2
Newbold, A.J.3
Sanderson, W.R.4
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35
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0035996943
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Casado-Bellver, F. J.; Gonzalez-Rosende, M. E.; Asensio, A.; Jorda-Gregori, J. M.; Alvarez-Sorolla, A.; Sepulveda-Arques, J. Orena, M.; Galeazzi, R. J. Chem. Soc., Perkin Trans. 1 2002, 1650.
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(2002)
J. Chem. Soc., Perkin Trans. 1
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Casado-Bellver, F.J.1
Gonzalez-Rosende, M.E.2
Asensio, A.3
Jorda-Gregori, J.M.4
Alvarez-Sorolla, A.5
Sepulveda-Arques, J.6
Orena, M.7
Galeazzi, R.8
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36
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0348101329
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note
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3, respectively.
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37
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0346840655
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note
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4 in methanol. Cbz-L-phenylalaninol and Cbz-D-phenylalaninol showed retention time 11.5 and 13.7 min, respectively, under the analysis conditions: Chiralpack (4.5 mm i.d. x 250 mm, Daicel, Japan), 210 nm, 1.0 mL/min, hexane/2-propanol = 90/10.
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38
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0348101330
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note
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In-process analysis showed that the reaction was completed in 6 h.
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39
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0348101331
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note
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Carbon tetrachloride is harmful to liver, kidney, and central nervous system. Exposure to 1000-2000 ppm for 30-60 min can be fatal to humans.
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