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6
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0001855961
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Schwab, P.; Grubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1996, 118, 100-110.
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Schwab, P.1
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9
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0000409956
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Niu, X.; Gopal, L.; Masingale, M. P.; Braden, D. A.; Hudson, B. S.; Sponsler, M. B. Organometallics 2000, 19, 649-660.
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Hudson, B.S.5
Sponsler, M.B.6
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10
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0035843056
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Sanford, M. S.; Love, J. A.; Grubbs, R. H. Organometallics 2001, 20, 5314-5318.
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Sanford, M.S.1
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11
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85034336744
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Love, J. A.; Morgan, J. P.; Trnka, T. M.; Grubbs, R. H. Angew. Chem., Int. Ed. 2002, 41, 4035-4037.
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Love, J.A.1
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0042020353
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Love, J. A.; Sanford, M. S.; Day, M. W.; Grubbs, R. H. J. Am. Chem. Soc. 2003, 125, 10103-10109.
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10144228427
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Romero, P. E.; Piers, W. E.; McDonald, R. Angew. Chem., Int. Ed. 2004, 43, 6161-6165.
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14
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0034814443
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15
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18444386352
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note
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1H NMR spectra taken within 2 min of addition show complete conversion.
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-
-
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16
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18444411158
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note
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18
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17
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7744223654
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Decomposition of metathesis-active ruthenium catalysts has been studied recently: (a) van Rensburg, W. J.; Steynberg, P. J.; Meyer, W. H.; Kirk, M. M.; Forman, G. S. J. Am. Chem. Soc. 2004, 126, 14332-14333.
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Van Rensburg, W.J.1
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Kirk, M.M.4
Forman, G.S.5
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18
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2942678732
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(b) Hong, S. H.; Day, M. W.; Grubbs, R. H. J. Am. Chem. Soc. 2004, 126, 7414-7415.
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Hong, S.H.1
Day, M.W.2
Grubbs, R.H.3
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20
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18444416970
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note
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1H NMR for complexes 4B and 2B, decomposition of 3B was observable only after approximately 3 h. Complexes 4B and 2B were fully decomposed overnight. In comparison, 1B was stable in this time frame.
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21
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0001754263
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31P NMR spectra of complex 2P were reported in: Chatterjee, A. K.; Sanders, D. P.; Grubbs, R. H. Org. Lett. 2002, 4, 1939-1942.
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Chatterjee, A.K.1
Sanders, D.P.2
Grubbs, R.H.3
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22
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0004233970
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published ASAP
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The complex was generated by reaction of 1P with cis-2-butene, propene, or 2-methyl-2-butene. Note added in proof: Complexes 2P, 2B, and 3P have appeared in a very recent report: Lehman, S. K., Jr.; Wagener, K. B. Organometallics 2005, published ASAP.
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Organometallics
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Lehman Jr., S.K.1
Wagener, K.B.2
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23
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0037416059
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Sworen, J. C.; Pawlow, J. H.; Case, W.; Lever, J.; Wagener, K. B. J. Mol. Catal. A: Chem. 2003, 194, 69-78.
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Sworen, J.C.1
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Case, W.3
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Wagener, K.B.5
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24
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0037420362
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Trnka, T. M.; Morgan, J. P.; Sanford, M. S.; Wilhelm, T. E.; Scholl, M.; Choi, T.-L.; Ding, S.; Day, M. W.; Grubbs, R. H. J. Am. Chem. Soc. 2003, 125, 2546-2558.
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Scholl, M.5
Choi, T.-L.6
Ding, S.7
Day, M.W.8
Grubbs, R.H.9
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26
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18444413816
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note
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-1. This likely indicates that near-saturation conditions exist at these higher concentrations. The small decrease can be attributed to either a solvent effect (2.0 M corresponds to a 1/2 alkene/C6D6 ratio) or experimental error.
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28
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18444400708
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Chem. Abstr. 2000, 132, 123053.
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Chem. Abstr.
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0033598258
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Scholl, M.; Ding, S.; Lee, C. W.; Grubbs, R. H. Org. Lett. 1999, 1, 953-956.
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Scholl, M.1
Ding, S.2
Lee, C.W.3
Grubbs, R.H.4
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30
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18444397594
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note
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6 at 25°C.
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-
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31
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18444384084
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note
-
3) was observed in the attempted catalytic reactions of 3P, consistent with deactivation by coordination. Another possible explanation is that 3P might contain an impurity that prevents catalysis.
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32
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4444244930
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Schuehler, D. E.; Williams, J. E.; Sponsler, M. B. Macromolecules 2004, 37, 6255-6257.
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Schuehler, D.E.1
Williams, J.E.2
Sponsler, M.B.3
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