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1
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0000036757
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Trost, B. M., Ed.; Pergamon Press: Oxford
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(a) Lee, D. G.; Chen, T. In Comprehensive Organic Synthesis; Trost, B. M., Ed.; Pergamon Press: Oxford, 1991; Vol. 7, pp 541-591.
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Comprehensive Organic Synthesis
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Lee, D.G.1
Chen, T.2
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5
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37049164430
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(a) Gillespie, D. T. C.; Jefferies, P. R.; Macbeth, A. K.; Thompson, M. J. J. Chem. Soc. 1955, 665.
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Gillespie, D.T.C.1
Jefferies, P.R.2
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Thompson, M.J.4
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6
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0000185122
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(b) Barrett, A. G. M.; Graboski, G. G.; Sabat, M.; Taylor, S. J. J. Org. Chem. 1987, 52, 4693.
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Barrett, A.G.M.1
Graboski, G.G.2
Sabat, M.3
Taylor, S.J.4
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8
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0030476308
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(d) Caron, S.; Stoermer, D.; Mapp, A. K.; Heathcock, C. H. J. Org. Chem. 1996, 61, 9126.
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Caron, S.1
Stoermer, D.2
Mapp, A.K.3
Heathcock, C.H.4
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9
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0028316810
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This alcohol has also been prepared by the treatment of 2-indanone with 2 equiv of the ylide derived from trimethylsulfonium bromide and base, which proceeds via the corresponding epoxide: Harnett, J. J.; Alcaraz, L.; Mioskowski, C.; Martel, J. P.; Gall, T. L.; Shin, D.-S.; Falck, J. R. Tetrahedron Lett. 1994, 35, 2009.
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(1994)
Tetrahedron Lett.
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, pp. 2009
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Harnett, J.J.1
Alcaraz, L.2
Mioskowski, C.3
Martel, J.P.4
Gall, T.L.5
Shin, D.-S.6
Falck, J.R.7
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10
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0012969141
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note
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1H NMR data is not reported, but this is consistent with our observations; an analogous mixture of free aldehyde, dimers, and higher oligomers could account for the variations in melting point.
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11
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0001475397
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(a) Tiffany, G. D.; Wright. J. B.; Moffett, R. B.; Heinzelman, R. V.; Strube, R. E.; Aspergren, B. D.; Lincoln, E. H.; White, J. L. J. Am. Chem. Soc. 1957, 79, 1682.
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Tiffany, G.D.1
Wright, J.B.2
Moffett, R.B.3
Heinzelman, R.V.4
Strube, R.E.5
Aspergren, B.D.6
Lincoln, E.H.7
White, J.L.8
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12
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0012922601
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(b) Taub, D.; Pettebone, R. H.; Wendler, N. L.: Tishler, M. J. Am. Chem. Soc. 1954, 76, 4094.
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Taub, D.1
Pettebone, R.H.2
Wendler, N.L.3
Tishler, M.4
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15
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0014259428
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(c) Inouye, S.; Tsuruoka. T.; Ito, T.; Niida, T. Tetrahedron 1968, 24, 2125.
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Tetrahedron
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Inouye, S.1
Tsuruoka, T.2
Ito, T.3
Niida, T.4
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16
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0025948431
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(d) Asahara, K.; Yamade, H.: Yoshida, S. Chem. Pharm. Bull. 1991, 39, 2662.
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(1991)
Chem. Pharm. Bull.
, vol.39
, pp. 2662
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Asahara, K.1
Yamade, H.2
Yoshida, S.3
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17
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0030990459
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(e) Dhavale, D. D.; Desai, V. N.; Sindkhedkar, M. D.; Mali, R. S.: Castellari, C.; Trombini, C. Tetrahedron: Asymmetry 1997, 8, 1475.
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(1997)
Tetrahedron: Asymmetry
, vol.8
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Dhavale, D.D.1
Desai, V.N.2
Sindkhedkar, M.D.3
Mali, R.S.4
Castellari, C.5
Trombini, C.6
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20
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33746873936
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(c) Schreiber, S. L.; Claus, R. E.; Reagan, J. Tetrahedron Lett. 1982, 23, 3867.
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(1982)
Tetrahedron Lett.
, vol.23
, pp. 3867
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Schreiber, S.L.1
Claus, R.E.2
Reagan, J.3
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22
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0012969307
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note
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This value corresponds to an overall heat flow including heat of reaction, heat of oxygen delivery, and heat of ozone addition and relates to the total heat that would need to be removed by the reactor jacket.
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23
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0001364416
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John Wiley & Sons: New York, Collect
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Bailey, P. S.; Erickson, R. E. In Organic Syntheses; John Wiley & Sons: New York, 1973; Collect. Vol. V, pp 489-493.
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(1973)
Organic Syntheses
, vol.5
, pp. 489-493
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Bailey, P.S.1
Erickson, R.E.2
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25
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0013007904
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Data generated by Chilworth Technology, Inc. Private communication of October 13, 2000
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Data generated by Chilworth Technology, Inc. Private communication of October 13, 2000.
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26
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0012922602
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note
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The experiment examined the solvent loss at the maximum gas flow rate of 200 L/min of total gas flow (150 L/min nitrogen in the reactor headspace and 50 L/min of air subsurface). The tank was charged with acetone (bp 56°C vs 65°C for MeOH), and resulted in a solvent loss of ca. 1 L/h at -70°C from an initial volume of 50 L. Acetone was chosen in place of methanol on the basis of its availability as a standard solvent for tank rinses and its slightly greater volatility.
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