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1
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0026730571
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1 Review: Afarinkia, K.; Vinader, V.; Nelson, T. D.; Posner, G. H. Tetrahedron 1992, 48, 9111-9171.
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(1992)
Tetrahedron
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Afarinkia, K.1
Vinader, V.2
Nelson, T.D.3
Posner, G.H.4
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2
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0013547497
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Harmata, M., Ed.; JAI: Greenwich, CT, in the press
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2 Sieburth, S. McN. In Advances in Cycloaddition; Harmata, M., Ed.; JAI: Greenwich, CT, 1999; Vol. 5; in the press.
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(1999)
In Advances in Cycloaddition
, vol.5
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Sieburth, S.M.1
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3
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0013516555
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3 Somekawa, K.; Shimou, T.; Tanaka, K.; Kumamoto, S. Chem. Lett. 1975, 45-46.
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(1975)
Chem. Lett.
, pp. 45-46
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Somekawa, K.1
Shimou, T.2
Tanaka, K.3
Kumamoto, S.4
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4
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0013557922
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4 Kanaoka, Y.; Ikeda, Y.; Sato, E. Heterocycles 1984, 21, 645.
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(1984)
Heterocycles
, vol.21
, pp. 645
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Kanaoka, Y.1
Ikeda, Y.2
Sato, E.3
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5
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85008108747
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Kaneko, C.; Suzuki, T.; Sato, M.; Naito, T. Chem. Pharm. Bull. 1987, 35, 112-123.
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(1987)
Chem. Pharm. Bull.
, vol.35
, pp. 112-123
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Kaneko, C.1
Suzuki, T.2
Sato, M.3
Naito, T.4
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7
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0013483752
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Sato, E.; Ikeda, Y.; Kanaoka, Y. Heterocycles 1989, 28, 117-120.
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(1989)
Heterocycles
, vol.28
, pp. 117-120
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Sato, E.1
Ikeda, Y.2
Kanaoka, Y.3
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10
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37049094898
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7 Nakamura, Y.; Kato, T.; Morita, Y. J. Chem. Soc., Perkin Trans. 1 1982, 1187-1191.
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(1982)
J. Chem. Soc., Perkin Trans. 1
, pp. 1187-1191
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Nakamura, Y.1
Kato, T.2
Morita, Y.3
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14
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0013546254
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note
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3) δ 170.2, 130.9, 130.8, 126.3, 121.3, 75.8, 72.5, 63.9, 56.6, .52.2, 41.9, 33.3, 20.9.
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16
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0000879089
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Yang, N. C.; Libman, J.; Savitzky, M. F. J. Am. Chem. Soc. 1972, 94, 9226-9227.
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(1972)
J. Am. Chem. Soc.
, vol.94
, pp. 9226-9227
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Yang, N.C.1
Libman, J.2
Savitzky, M.F.3
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18
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0013517374
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For an example of the use of furan to trap a reactive, photochemically-generated intermediate
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13 For an example of the use of furan to trap a reactive, photochemically-generated intermediate, see: Inoue, T.; Kaneda, T.; Misumi, S. Tetrahedron Lett. 1974, 2969-2972.
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(1974)
Tetrahedron Lett.
, pp. 2969-2972
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Inoue, T.1
Kaneda, T.2
Misumi, S.3
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19
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0001370462
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12 however rearrangement to a cyclooctadiene has not been reported. Other divinylcyclobutane rearrangements that lead to bicyclic structures include: A
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12 however rearrangement to a cyclooctadiene has not been reported. Other divinylcyclobutane rearrangements that lead to bicyclic structures include: A: Danheiser, R. L.; Gee, S. K.; Sard, H. J. Am. Chem. Soc. 1982, 104, 7670-7672.
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(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 7670-7672
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Danheiser, R.L.1
Gee, S.K.2
Sard, H.3
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20
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0001490724
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Trahanovsky, W. S.; Surber, B. W.; Wilkes, M. C.; Preckel, M. M. J. Am. Chem. Soc. 1982, 104, 6779-6781.
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(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 6779-6781
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Trahanovsky, W.S.1
Surber, B.W.2
Wilkes, M.C.3
Preckel, M.M.4
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21
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84985143795
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Huston, R.; Rey, M.; Dreiding, A. S. Helv. Chim. Acta 1982, 65, 451-467.
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(1982)
Helv. Chim. Acta
, vol.65
, pp. 451-467
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Huston, R.1
Rey, M.2
Dreiding, A.S.3
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24
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0001391098
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formula presented
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D: Majetich, G.; Hull, K.; Casares, A. M.; Khetani, V. J. Org. Chem. 1991, 56, 3958-3973. (formula presented)
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(1991)
J. Org. Chem.
, vol.56
, pp. 3958-3973
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Majetich, G.1
Hull, K.2
Casares, A.M.3
Khetani, V.4
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27
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0000660586
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17 West, F. G.; Chase, C. E.; Arif, A. M. J. Org. Chem. 1993, 58, 3794-3795.
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(1993)
J. Org. Chem.
, vol.58
, pp. 3794-3795
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West, F.G.1
Chase, C.E.2
Arif, A.M.3
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