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(d) Peterson, T. H.; Golden, J. T.; Bergman, R. G. J. Am. Chem. Soc. 2001, 123, 455-462.
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Kushch, K. A.; Lavrushko, V. V.; Misharin, Yu. S.; Moravsky, A. P.; Shilov, A. E. New J. Chem. 1983, 7, 729-733.
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Shilov, A.E.5
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0000738406
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(a) Stahl, S. S.; Labinger, J. A.; Bercaw, J. E. Angew. Chem., Int. Ed. 1998, 37, 2181-2192.
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Stahl, S.S.1
Labinger, J.A.2
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Periana, R. A.; Taube, D. J.; Gamble, S.; Taube, H.; Satoh, T.; Fujii, H. Science 1998, 250, 560-564.
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Periana, R.A.1
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12
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0035886138
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For a recent review of traditional "pincer" complexes of the platinum group metals see: Albrecht, M.; van Koten, G. Angew. Chem., Int. Ed. 2001, 40, 3750-3781.
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Albrecht, M.1
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0031053920
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(a) Holtcamp, M. W.; Labinger, J. A., Bercaw, J. E. J. Am. Chem. Soc. 1997, 119, 848-849.
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Holtcamp, M.W.1
Labinger, J.A.2
Bercaw, J.E.3
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16
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0030668913
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Goldberg and co-workers showed that an octahedral platinum(IV) species, resulting from C-H activation, can be stable to alkane loss by use of a potentially tripodal ligand. See: Wick, D. D.; Goldberg, K. I. J. Am. Chem. Soc. 1997, 119, 10235-10236.
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Wick, D.D.1
Goldberg, K.I.2
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17
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33748640712
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Cycloplatination reactions that result from orthometalation and generate acid have been described. See, for example: Ryabov, A. D.; van Eldik, R. Angew. Chem., Int. Ed. Engl. 1994, 33, 783-784.
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Angew. Chem., Int. Ed. Engl.
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Ryabov, A.D.1
Van Eldik, R.2
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18
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0038024980
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See the Supporting Information
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See the Supporting Information.
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19
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0038024979
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note
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The yield of 10 formed in this reaction critically depends on the purity of 9. Samples of 9 that do not give satisfactory combustion analysis invariably give much lower yields of 10.
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20
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0038363032
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note
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2BQA) system: addition of triflic acid to a benzene solution of 10 rapidly generates 9.
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21
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0037687013
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note
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2Et)][OTf], prior to the reaction with benzene.
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22
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0038363031
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note
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5
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