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Huang, C.-H.5
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(c) Curran, D. P.; Diederichsen, U.; Palovich, M. J. Am. Chem. Soc. 1997, 119, 4797-4804.
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Palovich, M.3
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10
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0000588661
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For other strategies to drive the equilibrium, see: (a) Hays, D. S.; Fu, G. C. J. Org. Chem. 1998, 63, 6375-6381.
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Hays, D.S.1
Fu, G.C.2
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14
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0000570983
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For homolytic 1,5-stannyl shift from carbon to oxygen, see: (a) Kim, S.; Lee, S.; Koh, J. S. J. Am. Chem. Soc. 1991, 113, 5106-5107.
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Kim, S.1
Lee, S.2
Koh, J.S.3
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16
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37049072571
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For homolytic 1,6-stannyl shift from carbon to oxygen, see: (a) Kim, S.; Lim, K. M. J. Chem. Soc., Chem. Commun. 1993, 1152-1153.
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Kim, S.1
Lim, K.M.2
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18
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0011782110
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For homolytic 1,4-stannyl shift from oxygen to oxygen, see: Alberti, A.; Hudson, A. Chem. Phy. Lett. 1977, 48, 331-333.
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Alberti, A.1
Hudson, A.2
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19
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0002849827
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For homolytic 1,5-stannyl shift from oxygen to oxygen, see: Davies, A. G.; Tse, M.-W. J. Organomet. Chem. 1978, 155, 25-30.
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Tse, M.-W.2
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23
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(a) Ho, T.-L.; Ho, H. C.; Wong, C. M. J. Chem. Soc., Chem. Commun. 1972, 791-791.
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(b) Ho, H. C.; Ho, T.-L.; Wong, C. M. Can. J. Chem. 1972, 50, 2718-2721.
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Ho, H.C.1
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25
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85034140142
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-
note
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The cyclization reaction was performed by slow addition (4 h) via syringe pump of a benzene solution of tributyltin hydride (1.3 equiv, 0.13 M in benzene) and AIBN (0.05 equiv) to a solution of the bromide (0.1 M) in refluxing benzene.
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27
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85034152550
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Butterworths: London, Chapter 11
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Pereyre, M.; Quintard, J.-P.; Rahm, A. Tin in Organic Synthesis; Butterworths: London, 1997; Chapter 11, p 261.
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Tin in Organic Synthesis
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Pereyre, M.1
Quintard, J.-P.2
Rahm, A.3
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28
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85034138581
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note
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A Rayonet photochemical reactor equipped with 3500 Å lamps was used.
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31
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0000072258
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de Mayo, P., Ed.; Academic Press: New York
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Beckwith, A. L. J.; Ingold, K. U. Rearrangements in ground and excited stares; de Mayo, P., Ed.; Academic Press: New York, 1980; Vol 1, pp 161-310.
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Rearrangements in Ground and Excited Stares
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Beckwith, A.L.J.1
Ingold, K.U.2
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32
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0005468161
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Nagai, M.; Lazor, J.; Wilcox, C. S. J. Org. Chem. 1990, 55, 3440-3442.
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Nagai, M.1
Lazor, J.2
Wilcox, C.S.3
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39
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85034153928
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note
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The stereochemistry of these compounds were determined by NOE experiments.
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