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4
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1542763298
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-
Grubbs, R. H.; Miller, S. J.; Fu, G. C. Acc. Chem. Res. 1995, 28, 446.
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Acc. Chem. Res.
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Grubbs, R.H.1
Miller, S.J.2
Fu, G.C.3
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5
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0037605726
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-
note
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Precursor 1a gives access to Ru-alkylidenes containing mono-, bi-, or tridentate phosphine ligands: (a) Volland, M. A. O.; Rominger, F.; Eisentrager, F.; Hofmann, P. J. Organomet. Chem. 2002, 641, 220.
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J. Organomet. Chem.
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Volland, M.A.O.1
Rominger, F.2
Eisentrager, F.3
Hofmann, P.4
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6
-
-
0000652909
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-
note
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(b) Amoroso, D.; Snelgrove, J. L.; Conrad, J. C.; Drouin, S. D.; Yap, G. P. A.; Fogg, D. E. Adv. Synth. Catal. 2002, 344, 757. We find that synthesis of 1a at -15 °C followed by warming to room temperature over 1.5 h, as in ref 3a, has no effect on formation of the carbyne byproduct but significantly increases bimolecular decomposition.
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(2002)
Adv. Synth. Catal.
, vol.344
, pp. 757
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-
Amoroso, D.1
Snelgrove, J.L.2
Conrad, J.C.3
Drouin, S.D.4
Yap, G.P.A.5
Fogg, D.E.6
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7
-
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0037943813
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-
note
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3).
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-
-
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8
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0035843056
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Sanford, M. S.; Love, J. A.; Grubbs, R. H. Organometallics 2001, 20, 5314.
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(2001)
Organometallics
, vol.20
, pp. 5314
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-
Sanford, M.S.1
Love, J.A.2
Grubbs, R.H.3
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9
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-
0033620417
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-
(a) Huang, J.; Stevens, E. D.; Nolan, S. P.; Peterson, J. L. J. Am. Chem. Soc. 1999, 121, 2674.
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J. Am. Chem. Soc.
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-
Huang, J.1
Stevens, E.D.2
Nolan, S.P.3
Peterson, J.L.4
-
10
-
-
0000335507
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-
(b) Huang, J.; Schanz, H.-J.; Stevens, E. D.; Nolan, S. P. Organometallics 1999, 18, 5375.
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(1999)
Organometallics
, vol.18
, pp. 5375
-
-
Huang, J.1
Schanz, H.-J.2
Stevens, E.D.3
Nolan, S.P.4
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11
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0033549782
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-
Weskamp, T.; Kohl, F. J.; Hieringer, W.; Gleich, D.; Herrmann, W. A. Angew. Chem., Int. Ed. 1999, 38, 2416.
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(1999)
Angew. Chem., Int. Ed.
, vol.38
, pp. 2416
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-
Weskamp, T.1
Kohl, F.J.2
Hieringer, W.3
Gleich, D.4
Herrmann, W.A.5
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12
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0000793212
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-
Arduengo, A. J.; Dias, H. V. R.; Harlow, R. L.; Kline, M. J. Am. Chem. Soc. 1992, 114, 5530.
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J. Am. Chem. Soc.
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-
Arduengo, A.J.1
Dias, H.V.R.2
Harlow, R.L.3
Kline, M.4
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13
-
-
0037943816
-
-
note
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3 with 3.
-
-
-
-
14
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-
0032476166
-
-
Alkyl-NHC analogues have been described: (a) Weskamp, T.; Schattenmann, W. C.; Spiegler, M.; Herrmann, W. A. Angew. Chem., Int. Ed. 1998, 37, 2490.
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(1998)
Angew. Chem., Int. Ed.
, vol.37
, pp. 2490
-
-
Weskamp, T.1
Schattenmann, W.C.2
Spiegler, M.3
Herrmann, W.A.4
-
16
-
-
0037042290
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-
Jazzar, R. F. R.; Macgregor, S. A.; Mahon, M. F.; Richards, S. P.; Whittlesey, M. K. J. Am. Chem. Soc. 2002, 124, 4944.
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J. Am. Chem. Soc.
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, pp. 4944
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-
Jazzar, R.F.R.1
Macgregor, S.A.2
Mahon, M.F.3
Richards, S.P.4
Whittlesey, M.K.5
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17
-
-
0037605730
-
-
note
-
This implies a smaller rotational barrier for 5a vs 4a: two trans-orthogonal "banana-shaped" IMes ligands are presumably permitted greater motion than an IMes ligand trans to the 3-D bulk of a phosphine ligand.
-
-
-
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18
-
-
0037605736
-
-
note
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2. A molecule of toluene solvent was located disordered at a 2-fold axis. All hydrogen atoms were treated as idealized contributions. All scattering factors are contained in the SHELXTL 6.12 program library (G. M. Sheldrick, Bruker AXS, Madison, WI, 2001). Crystallographic data (excluding structure factors) have been deposited with the Cambridge Crystallographic Data Centre as CCDC publication #203512. These data can be obtained free of charge on a application to the CCDC at 12 Union Road, Cambridge CB2 1EZ, U.K.; fax (+44) 1223-336-033; email deposit@ccdc.cam.ac.uk.
-
-
-
-
19
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0037420362
-
-
note
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2 complex were also reported, though bond lengths and angles are compromised by disorder between the two NHC ligands: 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.
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(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 2546
-
-
Trnka, T.M.1
Morgan, J.P.2
Sanford, M.S.3
Wilhelm, T.E.4
Scholl, M.5
Choi, T.-L.6
Ding, S.7
Day, M.W.8
Grubbs, R.H.9
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