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33645398022
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Dubs, C.; Yamamoto, T.; Inagaki, A.; Akita, M. Organometallics 2006, 25, 1344.
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Dubs, C.1
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Akita, M.4
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2
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33845378190
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(a) Schenk, T. G.; Downs, J. M.; Milne, C. R. C.; Mackenzie, P. B.; Boucher, H.; Whelan, J.; Bosnich, B. Inorg. Chem. 1985, 24, 2334.
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Schenk, T.G.1
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Boucher, H.5
Whelan, J.6
Bosnich, B.7
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3
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33845376678
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(b) Schenk, T. G.; Milne, C. R. C.; Sawyer, J. F.; Bosnich, B. Inorg. Chem. 1985, 24, 2338.
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Bosnich, B.4
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5
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33645413761
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note
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Complex 6 is obtained as a minor byproduct of the carbonylation and has been characterized only by X-ray crystallography. Crystallographic data are included in the Supporting Information.
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6
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33645380282
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5 but intractable mixtures of products were obtained, suggesting considerably different reactivity between the Rh and Ir analogues
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5 but intractable mixtures of products were obtained, suggesting considerably different reactivity between the Rh and Ir analogues.
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7
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0035800343
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(a) Tanaka, S.; Inagaki, A.; Akita M. Angew. Chem., Int, Ed. 2001, 40, 2865.
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Tanaka, S.1
Inagaki, A.2
Akita, M.3
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8
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1142293798
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(b) Tanaka, S.; Dubs, C.; Inagaki, A.; Akita, M. Organometallics 2004, 23, 317.
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Tanaka, S.1
Dubs, C.2
Inagaki, A.3
Akita, M.4
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9
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12444250061
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(c) Tanaka, S.; Dubs, C.; Inagaki, A.; Akita, M. Organometallics 2005, 24, 163.
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Tanaka, S.1
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11
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0001487886
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Lotz, S.; van Rooyen, P. H.; Meyer, R. Adv. Organomet. Chem. 1995, 37, 219.
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Lotz, S.1
Van Rooyen, P.H.2
Meyer, R.3
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12
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0003878171
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Academic: San Diego, CA
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Bovey, F. A.; Jelinski, L.; Mirau, P. A. Nuclear Magnetic Resonance Spectroscopy, 2nd ed.; Academic: San Diego, CA, 1988.
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Nuclear Magnetic Resonance Spectroscopy, 2nd Ed.
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Bovey, F.A.1
Jelinski, L.2
Mirau, P.A.3
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13
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33645395629
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note
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Because of the low quality of the crystal, the result for 10bb is not included in this paper. Crystal data for 10bb: triclinic, space group P1̄, a = 17.553(6) Å, b = 19.473(7) Å, c = 11.441(4) Å, α = 98.91(3)°, β = 90.17(2)°, γ = 65.268(9)°, V = 3500(2) Å3, Z = 4, T = -60 °C.
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14
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0000080999
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(a) Lichtenberger, D. L.; Renshaw, S. K.; Wong, A.; Tagge, C. D. Organometallics 1993, 12, 3522.
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Lichtenberger, D.L.1
Renshaw, S.K.2
Wong, A.3
Tagge, C.D.4
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15
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0000349421
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See also: (b) Lichtenberger, D. L.; Renshaw, S. K.; Bullock, R. M. J. Am. Chem. Soc. 1993, 115, 3276.
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Lichtenberger, D.L.1
Renshaw, S.K.2
Bullock, R.M.3
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17
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33645380729
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note
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From the reactions of the PNNN complexes 11 no characterizable product could be obtained.
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18
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33645405225
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note
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The cod complexes were converted to the corresponding CO complexes during the hydroformylation.
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21
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0037130740
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(a) Ozawa, F.; Okamoto, H.; Kawagishi, S.; Yamamoto, S.; Minami, T.; Yoshifuji, M. J. Am. Chem. Soc. 2002, 124, 10968.
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Ozawa, F.1
Okamoto, H.2
Kawagishi, S.3
Yamamoto, S.4
Minami, T.5
Yoshifuji, M.6
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22
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2342439178
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(b) Ozawa, F.; Ishiyama, T.; Yamamoto, S.; Kawagishi, S.; Murakami, H.; Yoshifuji, M. Organometallics 2004, 23, 1698.
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, pp. 1698
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Ozawa, F.1
Ishiyama, T.2
Yamamoto, S.3
Kawagishi, S.4
Murakami, H.5
Yoshifuji, M.6
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23
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33645390995
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(c) Bricout, H.; Carpentier, J,-F.; Mortreux, A. J. Mol Catal. A 1998, 136, 242.
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(1998)
Mol Catal. A
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Bricout, H.1
Carpentier, J.-F.2
Mortreux, A.J.3
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27
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0037239632
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(g) Kimura, M.; Futama, M.; Shibata, K.; Tamaru, Y. Chem. Commun. 2003, 234.
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Kimura, M.1
Futama, M.2
Shibata, K.3
Tamaru, Y.4
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28
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9144258517
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(h) García-Yebra, C.; Janssen, J. P.; Rominger, F.; Helmchen, G. Organometallics 2004, 23, 5459.
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García-Yebra, C.1
Janssen, J.P.2
Rominger, F.3
Helmchen, G.4
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29
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33645389628
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note
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13C NMR data and elemental analyses have not been obtained.
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