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Kira, M.1
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2
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33845378984
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a) S. Masamune, Y. Kabe, S. Collins, D. J. Williams, and R. Jones, J. Am. Chem. Soc., 107, 5552 (1985).
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b) R. Jones, D. J. Williams, Y. Kabe, and S. Masamune, Angew. Chem., Int. Ed. Engl., 25, 173 (1986).
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4
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Masamune, S.5
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5
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0000323809
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For reviews of interconversion among 1,3-butadiene, cyclobutene, and bicyclo[1.1.0]butane, see: (a) W. Leigh, Chem. Rev., 93, 487 (1993).
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Dolbier W.R., Jr.1
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W. Adam, T. Oppenländer, and G. Zang, J. Am. Chem. Soc., 107, 3921 (1985).
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Adam, W.1
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13
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0041296880
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note
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1 rate-determining 1,2-silyl migration in the two-step reaction via intermediary formation of the corresponding tetrasilacyclobutane-1,3-diyl diradical would also be compatible with the observed ΔS‡.
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-
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14
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0031441287
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8 a stable hexaaryltetrasila-1,3-butadiene was synthesized very recently: M. Weidenbruch, S. Willms, W. Saak, and G. Henkel, Angew. Chem., Int. Ed. Engl., 36, 2503 (1997).
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Weidenbruch, M.1
Willms, S.2
Saak, W.3
Henkel, G.4
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15
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0001615923
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and references cited therein
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An ab initio MO study has shown that tetrasila-1,3-butadiene is far more unstable than the most stable isomer, tetrasilabicyclo[1.1.0]-butane; the energy difference is 17.9 kcal/mol at the MP2/6-31G* level: M. Zhao and B. M. Gimarc, Inorg. Chem., 35, 5378 (1996), and references cited therein.
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Inorg. Chem.
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Zhao, M.1
Gimarc, B.M.2
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16
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0041296878
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note
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1,2 The spectral data of 6 are given in ref. 1.
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17
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0042298520
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note
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1H NMR spectroscopy to be more than 99%.
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-
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18
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0042298518
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note
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1H NMR spectroscopy have failed.
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22
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0001516654
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c) M. Ballestri, C. Chatgilialoglu, M. Lucarini, and G. F. Pedulli, J. Org. Chem., 57, 948 (1992).
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Ballestri, M.1
Chatgilialoglu, C.2
Lucarini, M.3
Pedulli, G.F.4
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23
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0041797337
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d) C. Chatgilialoglu, A. Guarini, A. Guerrini, and G. Seconi, J. Org. Chem., 57, 2208 (1992).
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Chatgilialoglu, C.1
Guarini, A.2
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Seconi, G.4
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