-
3
-
-
0036643424
-
-
Hillier A.C., Grasa G.A., Viciu M.S., Lee H.M., Yang C., and Nolan S.P. J. Organomet. Chem. 653 (2002) 69
-
(2002)
J. Organomet. Chem.
, vol.653
, pp. 69
-
-
Hillier, A.C.1
Grasa, G.A.2
Viciu, M.S.3
Lee, H.M.4
Yang, C.5
Nolan, S.P.6
-
12
-
-
33749349096
-
-
Herrmann W.A., Elison M., Fischer J., Köcher C., and Artus G.R.J. Angew. Chem.. Int. Ed. Engl. 34 (1995) 2371
-
(1995)
Angew. Chem.. Int. Ed. Engl.
, vol.34
, pp. 2371
-
-
Herrmann, W.A.1
Elison, M.2
Fischer, J.3
Köcher, C.4
Artus, G.R.J.5
-
17
-
-
18844421600
-
-
Singh R., Viciu M.S., Kramareva N., Navarro O., and Nolan S.P. Org. Lett. 7 (2005) 1829
-
(2005)
Org. Lett.
, vol.7
, pp. 1829
-
-
Singh, R.1
Viciu, M.S.2
Kramareva, N.3
Navarro, O.4
Nolan, S.P.5
-
22
-
-
14644438518
-
-
Yu K., Sommer W., Richardson J.M., Weck M., and Jones C.W. Adv. Synth. Catal. 347 (2005) 161
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 161
-
-
Yu, K.1
Sommer, W.2
Richardson, J.M.3
Weck, M.4
Jones, C.W.5
-
24
-
-
24944498445
-
-
Sommer W.J., Yu K., Sears J.S., Ji Y., Zheng X., Davis R.J., Sherrill C.D., Jones C.W., and Weck M. Organometallics 24 (2005) 4351
-
(2005)
Organometallics
, vol.24
, pp. 4351
-
-
Sommer, W.J.1
Yu, K.2
Sears, J.S.3
Ji, Y.4
Zheng, X.5
Davis, R.J.6
Sherrill, C.D.7
Jones, C.W.8
Weck, M.9
-
26
-
-
0034732513
-
-
Morales-Morales D., Grause C., Kasaoka K., Redon R., Cramer R.E., and Jensen C.M. Inorg. Chim. Acta. 300-302 (2000) 958
-
(2000)
Inorg. Chim. Acta.
, vol.300-302
, pp. 958
-
-
Morales-Morales, D.1
Grause, C.2
Kasaoka, K.3
Redon, R.4
Cramer, R.E.5
Jensen, C.M.6
-
32
-
-
0001703882
-
-
Gruber A.S., Zim D., Ebeling G., Monteiro A.L., and Dupont J. Org. Lett. 2 (2000) 1287
-
(2000)
Org. Lett.
, vol.2
, pp. 1287
-
-
Gruber, A.S.1
Zim, D.2
Ebeling, G.3
Monteiro, A.L.4
Dupont, J.5
-
36
-
-
0002956072
-
-
Terheijden J., Van Koten G., Van Beek J.A.M., Vriesema B.K., Kellogg R.M., Zoutberg M.C., and Stam C.H. Organometallics 6 (1987) 89
-
(1987)
Organometallics
, vol.6
, pp. 89
-
-
Terheijden, J.1
Van Koten, G.2
Van Beek, J.A.M.3
Vriesema, B.K.4
Kellogg, R.M.5
Zoutberg, M.C.6
Stam, C.H.7
-
37
-
-
33846869728
-
-
Reviews for the bis- and tris-NHC carbene complexes
-
Reviews for the bis- and tris-NHC carbene complexes. Pugh D., and Danopoulos A.A. Coord. Chem. Rev. 251 (2007) 610
-
(2007)
Coord. Chem. Rev.
, vol.251
, pp. 610
-
-
Pugh, D.1
Danopoulos, A.A.2
-
39
-
-
0035843070
-
-
Gründemann S., Albrecht M., Loch J.A., Faller J.W., and Crabtree R.H. Organometallics 20 (2001) 5485
-
(2001)
Organometallics
, vol.20
, pp. 5485
-
-
Gründemann, S.1
Albrecht, M.2
Loch, J.A.3
Faller, J.W.4
Crabtree, R.H.5
-
40
-
-
84962415029
-
-
Miecznikowski J.R., Grundemann S., Albrecht M., Mégret C., Clot E., Faller J.W., Eisenstein O., and Crabtree R.H. Dalton Trans. (2003) 831
-
(2003)
Dalton Trans.
, pp. 831
-
-
Miecznikowski, J.R.1
Grundemann, S.2
Albrecht, M.3
Mégret, C.4
Clot, E.5
Faller, J.W.6
Eisenstein, O.7
Crabtree, R.H.8
-
45
-
-
4444382495
-
-
The strong interaction between imidazole and imidazole cation was examined theoretically. See
-
The strong interaction between imidazole and imidazole cation was examined theoretically. See. Yan S., Bu Y., Cao Z., and Li P. J. Phys. Chem. A 108 (2004) 7038
-
(2004)
J. Phys. Chem. A
, vol.108
, pp. 7038
-
-
Yan, S.1
Bu, Y.2
Cao, Z.3
Li, P.4
-
46
-
-
67749092121
-
-
note
-
2) where kc is the rate constant at the coalescence point, Av is the difference in chemical shifts (in Hz), and J is coupling constant. The signals of the benzylic protons (signals of the methylene protons located between the NHC group and the phenyl group) appeared as coupled AB signals at low temperature, and they were analyzed to calculate the parameters.
-
-
-
-
47
-
-
0037765113
-
-
Pytkowicz J., Roland S., Mangeney P., Meyer G., and Jutand A. J. Organomet. Chem. 678 (2003) 166
-
(2003)
J. Organomet. Chem.
, vol.678
, pp. 166
-
-
Pytkowicz, J.1
Roland, S.2
Mangeney, P.3
Meyer, G.4
Jutand, A.5
-
48
-
-
67749126846
-
-
note
-
The decomposition of the Pd complexes to colloidal Pd might have occured at the elevated temparature (120 °C), since the color of the reaction mixure turned brown. The decomposition of the Pd catalyst seems to be suppressed at 80 °C (entries 5-6).
-
-
-
-
49
-
-
67749092531
-
-
note
-
Though we examined the reaction of some aryl bromides, the reactions proceeded very slowly, indicating the lower catalytic activity of the macrocyclic Pd complexes compared to the acyclic analogues. See, ref. 12a.
-
-
-
-
54
-
-
67749123610
-
-
note
-
Unless the Pd-C bond is cleaved, it is necessary to postulate a less stable Pd(III) complex as an intermediate.
-
-
-
-
56
-
-
0000576638
-
-
van de Kuil L.A., Luitjes H., Grove D.M., Zwikker J.W., van der Linden J.G.M., Roelofsen A.M., Jenneskens L.W., Drenth W., and van Koten G. Organometallics 13 (1994) 468
-
(1994)
Organometallics
, vol.13
, pp. 468
-
-
van de Kuil, L.A.1
Luitjes, H.2
Grove, D.M.3
Zwikker, J.W.4
van der Linden, J.G.M.5
Roelofsen, A.M.6
Jenneskens, L.W.7
Drenth, W.8
van Koten, G.9
|