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33751154737
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Ishii Y., Nakayama K., Takeno M., Sakagushi S., Iwahama T., and Nishiyama Y. J. Org. Chem. 60 (1995) 3934-3935
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24
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0011203958
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The syntheses of compounds 1-3 have been previously reported. Compound 1:
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The syntheses of compounds 1-3 have been previously reported. Compound 1:. Lutz J. J. Org. Chem. 36 (1971) 3835-3837
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Lutz, J.1
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25
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0035866586
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Compound 2:
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Compound 2:. Dutta A.K., Aloke K., Fei X.-S., Beardsley P.M., Newman J.L., and Reith M.E.A. J. Med. Chem. 44 (2001) 937-948
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26
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45949112772
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Compound 3:
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Compound 3:. Stanciuc G., Capriou M.T., Caragheorgheopol A., Caldaru H., Balaban A.T., and Walter R.I. J. Magn. Reson. 75 (1987) 63-72
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27
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34250848054
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note
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The reasons of these differences have been discussed in detail in Ref. 3a.
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28
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34250878794
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note
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The considerable absorbance above 300 nm shown by compounds 1 and 2 (ε = 2200 at 301 nm for 1) allows irradiation of sample solutions in pyrex glassware.
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-
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29
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34250890517
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note
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{radical dot}.
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31
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0001863407
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Pedulli G.F., Lucarini M., Pedrielli P., Sagrini M., and Cipollone M. Res. Chem. Intermed. 22 (1996) 1-14
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Pedulli, G.F.1
Lucarini, M.2
Pedrielli, P.3
Sagrini, M.4
Cipollone, M.5
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32
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34250868162
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note
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The time course of the photocatalytic reaction was monitored by GC-MS analysis.
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33
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33749003177
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Xia S., Villamena F.A., Hadad C.M., Kuppusamy P., Li Y., Zhu H., and Zweier J.L. J. Org. Chem. 71 (2006) 7268-7279
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Xia, S.1
Villamena, F.A.2
Hadad, C.M.3
Kuppusamy, P.4
Li, Y.5
Zhu, H.6
Zweier, J.L.7
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38
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34250900763
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note
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2 concentration present in the sample suggests that the decay process is not determined by the fate of the alkyl radical.
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