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For the X-ray studies of exo adducts: a) M. F. Semmelhack, H. T. Hall, Jr., R. Farina, M. Yoshifuji, G. Clark, T. Bargar, K. Hirotsu, J. Clardy, J. Am. Chem. Soc. 1979, 101, 3535.
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b) N. Tokitoh, Bull. Chem. Soc. Jpn. 2004, 77, 429, and references cited therein. For the recent examples:
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f) N. Tokitoh, A. Shinohara, T. Matsumoto, T. Sasamori, N. Takeda, Y. Furukawa, Organometallics 2007, 26, 4048. For the complexes, see:
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34250786751
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N. Tokitoh, N. Nakata, A. Shinohara, N. Takeda, T. Sasamori, Chem.-Eur. J. 2007, 13, 1856, see also ref. 4e.
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i) N. Tokitoh, N. Nakata, A. Shinohara, N. Takeda, T. Sasamori, Chem.-Eur. J. 2007, 13, 1856, see also ref. 4e.
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17
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a) K. Wakita, N. Tokitoh, R. Okazaki, S. Nagase, Angew. Chem., Int. Ed. 2000, 39, 634.
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Wakita, K.1
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18
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0034647203
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b) K. Wakita, N. Tokitoh, R. Okazaki, N. Takagi, S. Nagase, J. Am. Chem. Soc. 2000, 122, 5648.
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Wakita, K.1
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Nagase, S.5
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19
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49149114774
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6 resulted in the 50% conversion of 1 to 5.
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6 resulted in the 50% conversion of 1 to 5.
-
-
-
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20
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49149087654
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2O in THF was performed, 1:1 mixture of endo and exo adducts was obtained.
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2O in THF was performed, 1:1 mixture of endo and exo adducts was obtained.
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-
-
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21
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49149118027
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6]).
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6]).
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-
-
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22
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0035911980
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and references cited therein
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J. M. Dysard, T. D. Tilley, T. K. Woo, Organometallics 2001, 20, 1195, and references cited therein.
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Organometallics
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Dysard, J.M.1
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23
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0000767894
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H. G. Alt, H. E. Engelhardt, W. Kläui, A. Müller, J. Organomet. Chem. 1987, 331, 317.
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J. Organomet. Chem
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Alt, H.G.1
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24
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0000362655
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E. P. Kündig, D. Amurrio, G. Bernardinelli, R. Chowdhury, Organometallics 1993, 12, 4275.
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Organometallics
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Kündig, E.P.1
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Chowdhury, R.4
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25
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49149122079
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Supporting Information is available electronically on the CSJ-Journal Web site, http://www.csj.jp/journals/chem-lett/index.html.
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Supporting Information is available electronically on the CSJ-Journal Web site, http://www.csj.jp/journals/chem-lett/index.html.
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-
-
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26
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49149093100
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3] with silacyclohexa-1,4-diene 4 did not proceed.
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3] with silacyclohexa-1,4-diene 4 did not proceed.
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