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(b) Zhu, K.; Achord, P. D.; Zhang, X.; Krogh-Jespersen, K.; Goldman, A. S. J. Am. Chem. Soc. 2004, 126, 13044.
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Zhu, K.1
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6
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33751433553
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(d) Kuklin, S. A.; Sheloumov, A. M.; Dolgushin, F. M.; Ezernitskaya, M. G.; Peregudov, A. S.; Petrovskii, P. V.; Koridze, A. A. Organometallics 2006, 25, 5466.
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Kuklin, S.A.1
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Ezernitskaya, M.G.4
Peregudov, A.S.5
Petrovskii, P.V.6
Koridze, A.A.7
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8
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33645809744
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(f) Goldman, A. S.; Roy, A. H.; Huang, Z.; Ahuja, R.; Schinski, W.; Brookhart, M. Science 2006, 312, 257.
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Goldman, A.S.1
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9
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0003141829
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Dehydrogenation of THF: (a) Gupta, M.; Kaska, W. C.; Jensen, C. M. Chem. Commun. 1997, 461.
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Dehydrogenation of THF: (a) Gupta, M.; Kaska, W. C.; Jensen, C. M. Chem. Commun. 1997, 461.
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10
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0042567345
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Dehydrogenation of tertiary amines: (b) Zhang, X.; Fried, A.; Knapp, S.; Goldman, A. S. Chem. Commun. 2003, 2060.
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Dehydrogenation of tertiary amines: (b) Zhang, X.; Fried, A.; Knapp, S.; Goldman, A. S. Chem. Commun. 2003, 2060.
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12
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0030111075
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(a) Luecke, H. F.; Arndtsen, B. A.; Burger, P.; Bergman, R. G. J. Am. Chem. Soc. 1996, 118, 2517.
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Luecke, H.F.1
Arndtsen, B.A.2
Burger, P.3
Bergman, R.G.4
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14
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33244484149
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(c) Owen, J. S.; Labinger, J. A.; Bercaw, J. E. J. Am. Chem. Soc. 2006, 128, 2005.
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J. Am. Chem. Soc
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Owen, J.S.1
Labinger, J.A.2
Bercaw, J.E.3
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15
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33947144747
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(d) Alvarez, E.; Paneque, M.; Petronilho, A. G.; Poveda, M. L.; Santos, L. L.; Carmona, E.; Mereiter, K. Organometallics 2007, 26, 1231.
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Alvarez, E.1
Paneque, M.2
Petronilho, A.G.3
Poveda, M.L.4
Santos, L.L.5
Carmona, E.6
Mereiter, K.7
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16
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0031053920
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(e) Holtcamp, M. W.; Labinger, J. A.; Bercaw, J. E. J. Am. Chem. Soc. 1997, 119, 848.
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Holtcamp, M.W.1
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Bercaw, J.E.3
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17
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0001765251
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(f) Holtcamp, M. W.; Henling, L. M.; Day, M. W.; Labinger, J. A.; Bercaw, J. E. Inorg. Chim. Acta 1998, 270, 467.
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Holtcamp, M.W.1
Henling, L.M.2
Day, M.W.3
Labinger, J.A.4
Bercaw, J.E.5
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18
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0034806687
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(a) Fekl, U.; Kaminsky, W.; Goldberg, K. I. J. Am. Chem. Soc. 2001, 123, 6423.
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(2001)
J. Am. Chem. Soc
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Fekl, U.1
Kaminsky, W.2
Goldberg, K.I.3
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20
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0346848866
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(c) Fekl, U.; Kaminsky, W.; Goldberg, K. I. J. Am. Chem. Soc. 2003, 125, 15286.
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Fekl, U.1
Kaminsky, W.2
Goldberg, K.I.3
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21
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28944439469
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Similar results observed with (nacnac)Ir: Bernskoetter, W. H.; Lobkovsky, E.; Chirik, P. J. Organometallics 2005, 24, 6250.
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Similar results observed with (nacnac)Ir: Bernskoetter, W. H.; Lobkovsky, E.; Chirik, P. J. Organometallics 2005, 24, 6250.
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22
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35348933132
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An analogous procedure was used to synthesize (nacnac)Pt(Me)(SMe 2) where the nacnac ligands contain p-Cl or OMe substituents: (a) Iverson, C. N, Carter, C. A. G, Scollard, J. D, Pribisko, M. A, John, K. D, Scott, B. L, Baker, R. T, Bercaw, J. E, Labinger, J. A. ACS Symp. Ser. 2004, 885, 319
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2) where the nacnac ligands contain p-Cl or OMe substituents: (a) Iverson, C. N.; Carter, C. A. G.; Scollard, J. D.; Pribisko, M. A.; John, K. D.; Scott, B. L.; Baker, R. T.; Bercaw, J. E.; Labinger, J. A. ACS Symp. Ser. 2004, 885, 319.
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23
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35348940040
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The structure of 1b is given in the Supporting Information.
-
The structure of 1b is given in the Supporting Information.
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24
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0142040731
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2 in: Iverson, C. N.; Carter, C. A. G.; Baker, R. T.; Scollard, J. D.; Labinger, J. A.; Bercaw, J. E. J. Am. Chem. Soc. 2003, 125, 12674.
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2 in: Iverson, C. N.; Carter, C. A. G.; Baker, R. T.; Scollard, J. D.; Labinger, J. A.; Bercaw, J. E. J. Am. Chem. Soc. 2003, 125, 12674.
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-
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25
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35348954187
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2) is formed as a byproduct.
-
2) is formed as a byproduct.
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-
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26
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35348940041
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Pentene isomers were observed after 48 h at 50°C.
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Pentene isomers were observed after 48 h at 50°C.
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27
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34547531483
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(a) Chen, G. S.; Labinger, J. A.; Bercaw, J. E. Proc. Natl. Acad. Sci. U.S.A. 2007, 104, 6915.
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(2007)
Proc. Natl. Acad. Sci. U.S.A
, vol.104
, pp. 6915
-
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Chen, G.S.1
Labinger, J.A.2
Bercaw, J.E.3
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29
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24644447716
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Vetter, A. J.; Flaschenriem, C.; Jones, W. D. J. Am. Chem. Soc. 2005, 127, 12315.
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(2005)
J. Am. Chem. Soc
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, pp. 12315
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Vetter, A.J.1
Flaschenriem, C.2
Jones, W.D.3
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30
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35349019647
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-
Compound 2d was synthesized by adding excess TBE to 2c.
-
Compound 2d was synthesized by adding excess TBE to 2c.
-
-
-
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31
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35348988568
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1H NMR and GC.
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1H NMR and GC.
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-
-
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32
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35348973379
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Decomposition occurs rapidly above 60°C.
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Decomposition occurs rapidly above 60°C.
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