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37049088828
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and references cited therein
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Boyd, D. R.; Coulter, P. B.; McGuckin', M. R.; Sharma, N. D.; Jennings, W. B.; Wilson, V. E. J. Chem. Soc., Perkin Trans. 1 1990, 301 and references cited therein.
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1542757921
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Patai, S., Ed.; Wiley: New York, Chapter 21
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Tapuhi, Y.1
Grushka, E.2
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18
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37049116326
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(b) Bingham, K. D.; Blaiklock, T. M.; Coleman, R. C. B.; Meakins, G. D. J. Chem. Soc. (C) 1970, 2330.
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19
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0026003832
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(a) Marples, B. A.; Muxworthy, J. P.; Baggaley, K. H. Tetrahedron Lett. 1991, 32, 533.
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0000050003
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21
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0004165006
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2 solution and the oxidations should be carried out in a hood behind a safety shield and all protection measures exercised
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2 solution and the oxidations should be carried out in a hood behind a safety shield and all protection measures exercised.
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(1970)
Organic Peroxides
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Swern, D.1
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22
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1542443055
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2) and the higher leaving group tendency of the resulting arenesulfonate
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2) and the higher leaving group tendency of the resulting arenesulfonate.
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23
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1542443054
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The optimum pH range for the caroate-mediated generation of 1a has been established to be 7.5-8.0 (no formation of 1a is observed below pH 6.5 and above 8.5, see ref 8)
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The optimum pH range for the caroate-mediated generation of 1a has been established to be 7.5-8.0 (no formation of 1a is observed below pH 6.5 and above 8.5, see ref 8).
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24
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1542757920
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For a comparison concerning the oxidation by dioxiranes generated from caroate and molar amounts of the ketone, see ref 7 and 8
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For a comparison concerning the oxidation by dioxiranes generated from caroate and molar amounts of the ketone, see ref 7 and 8.
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25
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27844577489
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Edwards, J. O.; Pater, R. H.; Curci, R.; DiFuria, F. Photochem. Photobiol. 1979, 30, 63.
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Edwards, J.O.1
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DiFuria, F.4
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26
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0002653914
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16O exclusively, which indicate that no dioxirane is involved in the oxidation step. This contrary finding has been rationalized by the authors in terms of other oxidation mechanisms
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16O exclusively, which indicate that no dioxirane is involved in the oxidation step. This contrary finding has been rationalized by the authors in terms of other oxidation mechanisms.
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J. Chem. Soc., Chem. Commun.
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Armstrong, A.1
Clarke, P.A.2
Wood, A.3
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27
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1542547665
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note
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18OH.
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28
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0001204542
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(a) Adam, W.; Chan, Y. Y.; Cremer, D.; Scheutzow, D.; Schindler, M. J. Org. Chem. 1987, 52, 2800.
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1542652675
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Müller, E., Ed; Georg Thieme Verlag: Stuttgart
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