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1
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33845470390
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(a) Kirmse, W.; Rondan, N. G.; Houk, K. N. J. Am. Chem. Soc. 1984, 106, 7989.
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(1984)
J. Am. Chem. Soc.
, vol.106
, pp. 7989
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Kirmse, W.1
Rondan, N.G.2
Houk, K.N.3
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3
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0001280856
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(a) Dolbier, Jr. W. R.; Koroniak, H.; Burton, D. J.; Bailey, A. R.; Shaw, G. S.; Hansen, S. W. J. Am. Chem. Soc. 1984, 106, 1871.
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(1984)
J. Am. Chem. Soc.
, vol.106
, pp. 1871
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Dolbier Jr., W.R.1
Koroniak, H.2
Burton, D.J.3
Bailey, A.R.4
Shaw, G.S.5
Hansen, S.W.6
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4
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0001414464
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(b) Rudolf, K.; Spellmeyer, D. C.; Houk, K. N. J. Org. Chem. 1987, 52, 3708.
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(1987)
J. Org. Chem.
, vol.52
, pp. 3708
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Rudolf, K.1
Spellmeyer, D.C.2
Houk, K.N.3
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5
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0025802612
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(c) Hayes, R.; Ingham, S.; Saengchantara, S. T.; Wallace, T. W. Tetrahedron Lett. 1991, 32, 2953.
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(1991)
Tetrahedron Lett.
, vol.32
, pp. 2953
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Hayes, R.1
Ingham, S.2
Saengchantara, S.T.3
Wallace, T.W.4
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7
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0001060738
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(e) Jefford, C. W.; Bernardinelli, G.; Wang, Y.; Spellmeyer, D. C.; Buda, A.; Houk, K. N. J. Am. Chem. Soc. 1992, 114, 1157.
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(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 1157
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Jefford, C.W.1
Bernardinelli, G.2
Wang, Y.3
Spellmeyer, D.C.4
Buda, A.5
Houk, K.N.6
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9
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0029153147
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(g) Niwayama, S.; Wang, Y.; Houk, K. N. Tetrahedron Lett. 1995, 36, 6201
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(1995)
Tetrahedron Lett.
, vol.36
, pp. 6201
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Niwayama, S.1
Wang, Y.2
Houk, K.N.3
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10
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0035825169
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(a) Murakami, M.; Miyamoto, Y.; Ito, Y. Angew. Chem., Int. Ed. 2001, 40, 189.
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(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 189
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Murakami, M.1
Miyamoto, Y.2
Ito, Y.3
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11
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0034801316
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(b) Murakami, M.; Miyamoto, Y.; Ito, Y. J. Am. Chem. Soc. 2001, 123, 6441.
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(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 6441
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Murakami, M.1
Miyamoto, Y.2
Ito, Y.3
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12
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0037134883
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An analogous effect has been reported in the ring opening of oxetene: Shindo, M.; Matsumoto, K.; Mori, S.; Shishido, K. J. Am. Chem. Soc. 2002, 124, 6840.
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(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 6840
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Shindo, M.1
Matsumoto, K.2
Mori, S.3
Shishido, K.4
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13
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0037473524
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A recent theoretical paper by Houk et al. supports our interpretation: Lee, P. S.; Zhang, X.; Houk, K. N. J. Am. Chem. Soc. 2003, 125, 5072. For a different explanation assuming geminal σ bond participation, see: Ikeda, H.; Kato, T.; Inagaki, S. Chem. Lett. 2001, 270.
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(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 5072
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Lee, P.S.1
Zhang, X.2
Houk, K.N.3
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14
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0035532126
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A recent theoretical paper by Houk et al. supports our interpretation: Lee, P. S.; Zhang, X.; Houk, K. N. J. Am. Chem. Soc. 2003, 125, 5072. For a different explanation assuming geminal σ bond participation, see: Ikeda, H.; Kato, T.; Inagaki, S. Chem. Lett. 2001, 270.
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(2001)
Chem. Lett.
, pp. 270
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Ikeda, H.1
Kato, T.2
Inagaki, S.3
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16
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0000203981
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Niwayama, S.; Kallel, E. A.; Spellmeyer, D. C.; Chimin, C.; Houk, K. N. J. Org. Chem. 1996, 61, 2813.
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(1996)
J. Org. Chem.
, vol.61
, pp. 2813
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Niwayama, S.1
Kallel, E.A.2
Spellmeyer, D.C.3
Chimin, C.4
Houk, K.N.5
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17
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11944262103
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Kallel, E. A.; Wang, Y.; Spellmeyer, D. C.; Houk, K. N. J. Am. Chem. Soc. 1990, 112, 6759.
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(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 6759
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Kallel, E.A.1
Wang, Y.2
Spellmeyer, D.C.3
Houk, K.N.4
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18
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0347820005
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note
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Stereochemical assignments were based on the vicinal coupling constants of the olefinic protons: J = 13.2 Hz for (Z)-butadiene 9, and J = 19.2 Hz for (E)-butadiene 10.
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19
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0347820003
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note
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Corresponds to a 69:31 ratio at 140 °C.
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20
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0011083499
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Reed, A. E.; Curtiss, L. A.; Weinhold, F. Chem. Rev. 1988, 88, 899.
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(1988)
Chem. Rev.
, vol.88
, pp. 899
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Reed, A.E.1
Curtiss, L.A.2
Weinhold, F.3
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