-
4
-
-
0035743653
-
-
(b) Kraatz, H. B.; van der Boom, M. E.; Ben-David, Y.; Milstein, D. Isr. J. Chem. 2001, 41, 163.
-
(2001)
Isr. J. Chem.
, vol.41
, pp. 163
-
-
Kraatz, H.B.1
Van Der Boom, M.E.2
Ben-David, Y.3
Milstein, D.4
-
5
-
-
33748095350
-
-
For recent examples, see: (a)
-
For recent examples, see: (a) Takahashi, M.; Masui, K.; Sekiguchi, H.; Kobayashi, N.; Mori, A.; Funahashi, M.; Tamaoki, N. J. Am. Chem. Soc. 2006, 128, 10930.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 10930
-
-
Takahashi, M.1
Masui, K.2
Sekiguchi, H.3
Kobayashi, N.4
Mori, A.5
Funahashi, M.6
Tamaoki, N.7
-
6
-
-
33749509027
-
-
(b) Chen, X.; Goodhue, C. E.; Yu, J. Q. J. Am. Chem. Soc. 2006, 128, 12634.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 12634
-
-
Chen, X.1
Goodhue, C.E.2
Yu, J.Q.3
-
7
-
-
35048815950
-
-
(c) Stuart, D. R.; Villemure, E.; Fagnou, K. J. Am. Chem. Soc. 2007, 129, 12072.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 12072
-
-
Stuart, D.R.1
Villemure, E.2
Fagnou, K.3
-
8
-
-
47749125841
-
-
(d) Chi, S. H.; Hwang, S. J.; Chang, S. J. Am. Chem. Soc. 2008, 130, 9254.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 9254
-
-
Chi, S.H.1
Hwang, S.J.2
Chang, S.3
-
9
-
-
43449139728
-
-
(e) Potavathri, S.; Dumas, A. S.; Dwight, T. A.; Naumiec, G. R.; Hammann, J. M.; DeBoef, B. Tetrahedron Lett. 2008, 49, 4050.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 4050
-
-
Potavathri, S.1
Dumas, A.S.2
Dwight, T.A.3
Naumiec, G.R.4
Hammann, J.M.5
DeBoef, B.6
-
10
-
-
0001412629
-
-
For representative examples, see: (a)
-
For representative examples, see: (a) Temple, J. S.; Riediker, M.; Schwartz, J. J. Am. Chem. Soc. 1982, 104, 1310.
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 1310
-
-
Temple, J.S.1
Riediker, M.2
Schwartz, J.3
-
11
-
-
0035354661
-
-
(b) Albeniz, A. C.; Espinet, P.; Martin-Ruiz, B. Chem. Eur. J. 2001, 7, 2481.
-
(2001)
Chem. Eur. J.
, vol.7
, pp. 2481
-
-
Albeniz, A.C.1
Espinet, P.2
Martin-Ruiz, B.3
-
12
-
-
30744445455
-
-
(c) Chen, X.; Li, J.-J.; Hao, X.-S.; Goodhue, C. E.; Yu, J.-Q. J. Am. Chem. Soc. 2006, 128, 78.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 78
-
-
Chen, X.1
Li, J.-J.2
Hao, X.-S.3
Goodhue, C.E.4
Yu, J.-Q.5
-
14
-
-
68549092330
-
-
(e) Perez-Rodriquez, M.; Braga, A. A. C.; Garcia-Melchor, M.; Perez-Temprano, M. H.; Casares, J. A.; Ujaque, G.; de Lera, A. R.; Alvarez, R.; Maseras, F.; Espinet, P. J. Am. Chem. Soc. 2009, 131, 3650.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 3650
-
-
Perez-Rodriquez, M.1
Braga, A.A.C.2
Garcia-Melchor, M.3
Perez-Temprano, M.H.4
Casares, J.A.5
Ujaque, G.6
De Lera, A.R.7
Alvarez, R.8
Maseras, F.9
Espinet, P.10
-
16
-
-
68249138163
-
-
- chemical oxidants such as Ce(IV) have also been recently reported
-
- chemical oxidants such as Ce(IV) have also been recently reported: Mei, T.-S.; Wang, X.; Yu, J.-Q. J. Am. Chem. Soc. 2009, 131, 10806.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 10806
-
-
Mei, T.-S.1
Wang, X.2
Yu, J.-Q.3
-
18
-
-
70350681484
-
-
note
-
•+. See Supporting Information for details.
-
-
-
-
19
-
-
70350630963
-
-
note
-
+.
-
-
-
-
20
-
-
70350687153
-
-
note
-
+/0 in acetone. See Supporting Information.
-
-
-
-
22
-
-
22944442589
-
-
+. However, the electron-rich, rigid nature of the starting material in this report and the presence of a pendant pyrazolyl arm and a chelating alkyl/aryl ligand are expected to render this example mechanistically very different from the current system
-
+. However, the electron-rich, rigid nature of the starting material in this report and the presence of a pendant pyrazolyl arm and a chelating alkyl/aryl ligand are expected to render this example mechanistically very different from the current system. Campora, J.; Palma, P.; del Rio, D.; Lopez, J. A.; Alvarez, E.; Connelly, N. G. Organometallics 2005, 24, 3624.
-
(2005)
Organometallics
, vol.24
, pp. 3624
-
-
Campora, J.1
Palma, P.2
Del Rio, D.3
Lopez, J.A.4
Alvarez, E.5
Connelly, N.G.6
-
23
-
-
44649179890
-
-
(a) Hager, E.; Sivaramakrishna, A.; Clayton, H. S.; Mogorosi, M. M.; Moss, J. R. Coord. Chem. Rev. 2008, 252, 1668.
-
(2008)
Coord. Chem. Rev.
, vol.252
, pp. 1668
-
-
Hager, E.1
Sivaramakrishna, A.2
Clayton, H.S.3
Mogorosi, M.M.4
Moss, J.R.5
-
24
-
-
0036006346
-
-
(b) Fooladi, E.; Graham, T.; Turner, M. L.; Dalhus, B.; Maitlis, P. M.; Tilset, M. J. Chem. Soc., Dalton Trans. 2002, 975.
-
(2002)
J. Chem. Soc., Dalton Trans.
, pp. 975
-
-
Fooladi, E.1
Graham, T.2
Turner, M.L.3
Dalhus, B.4
Maitlis, P.M.5
Tilset, M.6
-
27
-
-
0000259946
-
-
(e) Lau, W.; Huffman, J. C.; Kochi, J. K. Organometallics 1982, 1, 155.
-
(1982)
Organometallics
, vol.1
, pp. 155
-
-
Lau, W.1
Huffman, J.C.2
Kochi, J.K.3
-
29
-
-
0000788047
-
-
(a) Johansson, L.; Ryan, O. B.; Romming, C.; Tilset, M. Organometallics 1998, 17, 3957.
-
(1998)
Organometallics
, vol.17
, pp. 3957
-
-
Johansson, L.1
Ryan, O.B.2
Romming, C.3
Tilset, M.4
-
31
-
-
70350630962
-
-
note
-
•+. The same argument likely applies to the disproportionation in Scheme 2, mechanism B.
-
-
-
-
32
-
-
70350638052
-
-
note
-
+ and then conproportionation of the resulting bis-solvento complex with 1.
-
-
-
-
34
-
-
70350677357
-
-
note
-
6 scramble in room light.
-
-
-
-
35
-
-
0001651317
-
-
Hawari, J. A.; Engel, P. S.; Griller, D. Int. J. Chem. Kin. 1985, 17, 1215.
-
(1985)
Int. J. Chem. Kin.
, vol.17
, pp. 1215
-
-
Hawari, J.A.1
Engel, P.S.2
Griller, D.3
-
37
-
-
70350649396
-
-
note
-
+ oxidizes I- significantly more slowly than it does 1 under these conditions.
-
-
-
-
38
-
-
0001147716
-
-
For related 2,2′-bipyridyl complexes, see: (a)
-
For related 2,2′-bipyridyl complexes, see: (a) Byers, P. K.; Canty, A. J.; Crespo, M.; Puddephatt, R. J.; Scott, J. D. Organometallics 1988, 7, 1363.
-
(1988)
Organometallics
, vol.7
, pp. 1363
-
-
Byers, P.K.1
Canty, A.J.2
Crespo, M.3
Puddephatt, R.J.4
Scott, J.D.5
-
39
-
-
0000913252
-
-
(b) Aye, K.-T.; Canty, A. J.; Crespo, M.; Puddephatt, R. J.; Scott, J. D.; Watson, A. A. Organometallics 1989, 8, 1518.
-
(1989)
Organometallics
, vol.8
, pp. 1518
-
-
Aye, K.-T.1
Canty, A.J.2
Crespo, M.3
Puddephatt, R.J.4
Scott, J.D.5
Watson, A.A.6
-
40
-
-
0000045685
-
-
(c) Byers, P. K.; Canty, A. J.; Skelton, B. W.; Traill, P. R.; Watson, A. A.; White, A. H. Organometallics 1992, 11, 3085.
-
(1992)
Organometallics
, vol.11
, pp. 3085
-
-
Byers, P.K.1
Canty, A.J.2
Skelton, B.W.3
Traill, P.R.4
Watson, A.A.5
White, A.H.6
-
42
-
-
0010890993
-
-
(e) Dücker-Benfer, C.; van Eldik, R.; Canty, A. J. Organometallics 1994, 13, 2412.
-
(1994)
Organometallics
, vol.13
, pp. 2412
-
-
Dücker-Benfer, C.1
Van Eldik, R.2
Canty, A.J.3
-
43
-
-
70350645843
-
-
note
-
+ reaction at-80 °C. See Supporting Information for details.
-
-
-
-
44
-
-
67650511260
-
-
For a closely related dimeric Pt(III) complex, see
-
For a closely related dimeric Pt(III) complex, see: Canty, A. J.; Gardiner, M. G.; Jones, R. C.; Rodemann, T.; Sharma, M. J. Am. Chem. Soc. 2009, 131, 7236.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 7236
-
-
Canty, A.J.1
Gardiner, M.G.2
Jones, R.C.3
Rodemann, T.4
Sharma, M.5
-
45
-
-
33750288439
-
-
For examples of dimeric Pd(III) species, see: (a)
-
For examples of dimeric Pd(III) species, see: (a) Cotton, F. A.; Koshevoy, I. O.; Lahuerta, P.; Murillo, C. A.; Sanau, M.; Ubeda, M. A.; Zhao, Q. J. Am. Chem. Soc. 2006, 128, 13674.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 13674
-
-
Cotton, F.A.1
Koshevoy, I.O.2
Lahuerta, P.3
Murillo, C.A.4
Sanau, M.5
Ubeda, M.A.6
Zhao, Q.7
-
48
-
-
70350627924
-
-
note
-
The data do not exclude mechanism C at > -30 °C where 3 is not observed; however there is no evidence for a change in mechanism with temperature.
-
-
-
-
49
-
-
0000121328
-
-
Arsenault, G. L.; Anderson, C. M.; Puddephatt, R. J. Organometallics 1988, 7, 2094.
-
(1988)
Organometallics
, vol.7
, pp. 2094
-
-
Arsenault, G.L.1
Anderson, C.M.2
Puddephatt, R.J.3
-
51
-
-
70350667021
-
-
note
-
At ≤ -30 °C, intermediate 5 is stable so it is not possible to directly observe 3 in this system.
-
-
-
-
52
-
-
0001113218
-
-
Milani, B.; Anzilutti, A.; Vicentini, L.; Santi, A. S.; Zangrando, E.; Geremia, S.; Mestroni, G. Organometallics 1997, 16, 5064.
-
(1997)
Organometallics
, vol.16
, pp. 5064
-
-
Milani, B.1
Anzilutti, A.2
Vicentini, L.3
Santi, A.S.4
Zangrando, E.5
Geremia, S.6
Mestroni, G.7
-
53
-
-
70350639977
-
-
note
-
A small amount of hydroquinone (3.5 ± 1.7%) was also formed, presumably by protonation of 6 with trace acid. (Similar observations have been reported for the bpy analogue, ref 30.).
-
-
-
-
54
-
-
70350663418
-
-
note
-
1H NMR revealed an induction period, indicating a complex mechanistic pathway.
-
-
-
|