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10944226191
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Attempts to generate derivatives of bicyclo[1.1.0]butane or tetrasilabicyclo[1.1.0]butane dianions caused the unavoidable breaking of the central bridging bond, which results in the formation of cyclobutane-1,3-diides, which were subsequently trapped with appropriate electrophiles: a) W. R. Moore, S. S. Hall, C. Largman, Tetrahedron Lett, 1969, 4353;
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0037951591
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V. Ya. Lee, K. Takanashi, M. Ichinohe, A. Sekiguchi, J. Am. Chem. Soc. 2003, 125, 6012.
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Lee, V.Ya.1
Takanashi, K.2
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Sekiguchi, A.4
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1842841120
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V. Ya. Lee, K. Takanashi, T. Matsuno, M. Ichinohe, A. Sekiguchi, J. Am. Chem. Soc. 2004, 126, 4758.
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Sekiguchi, A.5
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10944244869
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note
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0). All structures were solved by the direct method and refined by the full matrix Least-squares method using SHELXL-97 program. CCDC-246460 (2a), CCDC-246461 (2b), CCDC-246462 (2c) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/ retrieving.html (or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB21EZ, UK; fax: (+44) 1223-336-033; or deposit@ccdc.cam.ac.uk).
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28
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0037190074
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V. Ya. Lee, M. Ichinohe, A. Sekiguchi, J. Am. Chem. Soc. 2002, 124, 9962.
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J. Am. Chem. Soc.
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Lee, V.Ya.1
Ichinohe, M.2
Sekiguchi, A.3
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0034694739
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The possibility of such isomeric interconversion incorporating the heavier Group 14 elements has been experimentally observed and discussed; see: a) V. Ya. Lee, M. Ichinohe, A. Sekiguchi, J. Am. Chem. Soc. 2000, 122, 12604;
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(2000)
J. Am. Chem. Soc.
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Lee, V.Ya.1
Ichinohe, M.2
Sekiguchi, A.3
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10944230175
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note
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b) see Ref. [9];
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0942288220
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Recently this topic was also studied theoretically; see: c) I. Özkan, A. Kinal, M. Balci, J. Phys. Chem. A 2004, 108, 507.
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(2004)
J. Phys. Chem. A
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Özkan, I.1
Kinal, A.2
Balci, M.3
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32
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10944243339
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note
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All theoretical calculations were performed at the B3LYP/6-31(d) level with the GAUSSIAN-98 program package.
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