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1
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33846104560
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For a selection of recent noteworthy examples, see: a
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For a selection of recent noteworthy examples, see: (a) Lu, C. C.; Saouma, C. T.; Day, M. W.; Peters, J. C. J. Am. Chem. Soc. 2007, 129, 4.
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Lu, C.C.1
Saouma, C.T.2
Day, M.W.3
Peters, J.C.4
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4
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33748481759
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(d) Ritter, T.; Day, M. W.; Grubbs, R. H. J. Am. Chem. Soc. 2006, 128, 11768.
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Ritter, T.1
Day, M.W.2
Grubbs, R.H.3
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5
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33746256415
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(e) Fout, A. R.; Basuli, F.; Fan, H.; Tomaszewski, J.; Huffman, J. C.; Baik, M.-H.; Mindiola, D. J. Angew. Chem., Int. Ed. 2006, 45, 3291.
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Fout, A.R.1
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Huffman, J.C.5
Baik, M.-H.6
Mindiola, D.J.7
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6
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2542473311
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(f) Turculet, L.; Feldman, J. D.; Tilley, T. D. Organometallics 2004, 23, 2488.
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Turculet, L.1
Feldman, J.D.2
Tilley, T.D.3
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7
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33751154664
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Johnson, T. J.; Folting, K.; Streib, W. E.; Martin, J. D.; Huffman, J. C.; Jackson, S. A.; Eisenstein, O.; Caulton, K. G. Inorg. Chem. 1995, 34, 488.
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Inorg. Chem
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Johnson, T.J.1
Folting, K.2
Streib, W.E.3
Martin, J.D.4
Huffman, J.C.5
Jackson, S.A.6
Eisenstein, O.7
Caulton, K.G.8
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8
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33744455063
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For two notable examples in Ru chemistry, see: a
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For two notable examples in Ru chemistry, see: (a) Zhang, J.; Leitus, G.; Ben-David, Y.; Milstein, D. Angew. Chem., Int. Ed. 2006, 45, 1113.
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(2006)
Angew. Chem., Int. Ed
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Zhang, J.1
Leitus, G.2
Ben-David, Y.3
Milstein, D.4
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10
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27544502994
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(a) Trost, B. M.; Frederiksen, M. U.; Rudd, M. T. Angew. Chem., Int. Ed. 2005, 44, 6630.
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Angew. Chem., Int. Ed
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Trost, B.M.1
Frederiksen, M.U.2
Rudd, M.T.3
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12
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1142274757
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(c) Davies, S. G.; McNally, J. P.; Smallridge, A. J. Adv. Inorg. Chem. 1990, 30, 1.
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(1990)
Adv. Inorg. Chem
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Davies, S.G.1
McNally, J.P.2
Smallridge, A.J.3
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13
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0242407297
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+-catalyzed hydrosilylation of alkenes, see: Glaser, P. B.; Tilley, T. D. J. Am. Chem. Soc. 2003, 125, 13640.
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+-catalyzed hydrosilylation of alkenes, see: Glaser, P. B.; Tilley, T. D. J. Am. Chem. Soc. 2003, 125, 13640.
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14
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27144462031
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(a) Rankin, M. A.; McDonald, R.; Ferguson, M. J.; Stradiotto, M. Organometallics 2005, 24, 4981.
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(2005)
Organometallics
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, pp. 4981
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Rankin, M.A.1
McDonald, R.2
Ferguson, M.J.3
Stradiotto, M.4
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15
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20544451120
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(b) Rankin, M. A.; McDonald, R.; Ferguson, M. J.; Stradiotto, M. Angew. Chem., Int. Ed. 2005, 44, 3603.
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(2005)
Angew. Chem., Int. Ed
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Rankin, M.A.1
McDonald, R.2
Ferguson, M.J.3
Stradiotto, M.4
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16
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34249090233
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2-indene is available from Strem Chemicals.
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2-indene is available from Strem Chemicals.
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-
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17
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3142749086
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The structural features in 3 compare well with those found in complexes featuring a P-Ru-C ring: Cadierno, V.; Díez, J.; García-Álvarez, J.; Gimeno, J. Organometallics 2004, 23, 3425 and references cited therein.
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The structural features in 3 compare well with those found in complexes featuring a P-Ru-C ring: Cadierno, V.; Díez, J.; García-Álvarez, J.; Gimeno, J. Organometallics 2004, 23, 3425 and references cited therein.
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-
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18
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33750731982
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3) linkages in some recently reported Ru chelate complexes: (a) Kuznetsov, V. F.; Abdur-Rashid, K.; Lough, A. J.; Gusev, D. G. J. Am. Chem. Soc. 2006, 128, 14388.
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3) linkages in some recently reported Ru chelate complexes: (a) Kuznetsov, V. F.; Abdur-Rashid, K.; Lough, A. J.; Gusev, D. G. J. Am. Chem. Soc. 2006, 128, 14388.
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19
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21244465818
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(b) Bibal, C.; Smurnyy, Y. D.; Pink, M.; Caulton, K. G. J. Am. Chem. Soc. 2005, 127, 8944.
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(2005)
J. Am. Chem. Soc
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Bibal, C.1
Smurnyy, Y.D.2
Pink, M.3
Caulton, K.G.4
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20
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1542315167
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(c) Bibal, C.; Pink, M.; Smurnyy, Y. D.; Tomaszewski, J.; Caulton, K. G. J. Am. Chem. Soc. 2004, 126, 2312.
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(2004)
J. Am. Chem. Soc
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-
Bibal, C.1
Pink, M.2
Smurnyy, Y.D.3
Tomaszewski, J.4
Caulton, K.G.5
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21
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33847183185
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(a) Cipot, J.; McDonald, R.; Ferguson, M. J.; Schatte, G.; Stradiotto, M. Organometallics 2007, 26, 594.
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(2007)
Organometallics
, vol.26
, pp. 594
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Cipot, J.1
McDonald, R.2
Ferguson, M.J.3
Schatte, G.4
Stradiotto, M.5
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22
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33644528459
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(b) Wile, B. M.; Burford, R. J.; McDonald, R.; Ferguson, M. J.; Stradiotto, M. Organometallics 2006, 25, 1028.
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(2006)
Organometallics
, vol.25
, pp. 1028
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Wile, B.M.1
Burford, R.J.2
McDonald, R.3
Ferguson, M.J.4
Stradiotto, M.5
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23
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34249074079
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6; details of this reaction will be described elsewhere,
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6; details of this reaction will be described elsewhere,
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-
-
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24
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34249053851
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Diagnostic NMR data for 7: 1H NMR (C 6D6) δ 10.30 (s, 1H, Ru=CH, 5.72 (d, J, 4.1 Hz, 1H, Cl-H, 9.21 (d, 2JPH, 24.3 Hz, 1H, Ru-H, 31P{1H} NMR (C6D6) δ 54.1. Diagnostic NMR data for 8: 1H NMR (C6D 6) δ 9.68 (s, 1H, Ru=CH, 5.96 (d, J, 3.7 Hz, 1H, Cl-H, 5.10 (s, 1H, Si-H, 9.90 (d, 2JPH, 25.2 Hz, 1H. Ru-H, 31P{1H} NMR (C6D6) δ 54.8
-
6) δ 54.8.
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-
-
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25
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34249038656
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3 was observed to generate an intractable mixture of products.
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3 was observed to generate an intractable mixture of products.
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-
-
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26
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34249021739
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A possible mechanism is provided in Scheme S1 of the Supporting Information.
-
(d) A possible mechanism is provided in Scheme S1 of the Supporting Information.
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