-
3
-
-
0001077422
-
-
a) R. R. Schrock, J. S. Murdzek, G. C. Bazan, J. Robbins, M. Dimare, M. O'Regan, J. Am. Chem. Soc. 1990, 112, 3875-3886;
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 3875-3886
-
-
Schrock, R.R.1
Murdzek, J.S.2
Bazan, G.C.3
Robbins, J.4
Dimare, M.5
O'Regan, M.6
-
5
-
-
0001855961
-
-
P. Schwab, R. H. Grubbs, J. W. Ziller, J. Am. Chem. Soc. 1996, 118, 100-110.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 100-110
-
-
Schwab, P.1
Grubbs, R.H.2
Ziller, J.W.3
-
6
-
-
0001249050
-
-
3 salts as metathesis catalysts demonstrated the high functional group tolerance of ruthenium, see: a) H. H. Thoi, K. J. Ivin, J. J. Rooney, J. Mol. Catal. 1982, 15, 245-270;
-
(1982)
J. Mol. Catal.
, vol.15
, pp. 245-270
-
-
Thoi, H.H.1
Ivin, K.J.2
Rooney, J.J.3
-
8
-
-
0033620417
-
-
a) J. Huang, E. D. Stevens, S. P. Nolan, J. L. Peterson, J. Am. Chem. Soc. 1999, 121, 2674-2678;
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 2674-2678
-
-
Huang, J.1
Stevens, E.D.2
Nolan, S.P.3
Peterson, J.L.4
-
9
-
-
0033582991
-
-
b) M. Scholl, T. M. Trnka, J. P. Morgan, R. H. Grubbs, Tetrahedron Lett. 1999, 40, 2247-2250;
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 2247-2250
-
-
Scholl, M.1
Trnka, T.M.2
Morgan, J.P.3
Grubbs, R.H.4
-
10
-
-
0001587279
-
-
c) T. Weskamp, F. J. Kohl, W. Hieringer, D. Gleich, W. A. Herrmann, Angew. Chem. 1999, 111, 2573-2576; Angew. Chem. Int. Ed. 1999, 38, 2416-2419;
-
(1999)
Angew. Chem.
, vol.111
, pp. 2573-2576
-
-
Weskamp, T.1
Kohl, F.J.2
Hieringer, W.3
Gleich, D.4
Herrmann, W.A.5
-
11
-
-
0033549782
-
-
c) T. Weskamp, F. J. Kohl, W. Hieringer, D. Gleich, W. A. Herrmann, Angew. Chem. 1999, 111, 2573-2576; Angew. Chem. Int. Ed. 1999, 38, 2416-2419;
-
(1999)
Angew. Chem. Int. Ed.
, vol.38
, pp. 2416-2419
-
-
-
12
-
-
0000335507
-
-
d) J. Huang, H.-J. Schanz, E. D. Stevens, S. P. Nolan, Organometallics 1999, 18, 5375-5380.
-
(1999)
Organometallics
, vol.18
, pp. 5375-5380
-
-
Huang, J.1
Schanz, H.-J.2
Stevens, E.D.3
Nolan, S.P.4
-
13
-
-
0033598258
-
-
M. Scholl, S. Ding, C. W. Lee, R. H. Grubbs, Org. Lett. 1999, 1, 953-956.
-
(1999)
Org. Lett.
, vol.1
, pp. 953-956
-
-
Scholl, M.1
Ding, S.2
Lee, C.W.3
Grubbs, R.H.4
-
14
-
-
0034685462
-
-
A. K. Chatterjee, J. P. Morgan, M. Scholl, R. H. Grubbs, J. Am. Chem. Soc. 2000, 122, 3783-3784.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 3783-3784
-
-
Chatterjee, A.K.1
Morgan, J.P.2
Scholl, M.3
Grubbs, R.H.4
-
15
-
-
0033603294
-
-
L. Ackermann, A. Füstner, T. Weskamp, F. J. Kohl, W. A. Herrmann, Tetrahedron Lett. 1999, 40, 4787-4790.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 4787-4790
-
-
Ackermann, L.1
Füstner, A.2
Weskamp, T.3
Kohl, F.J.4
Herrmann, W.A.5
-
17
-
-
0001433830
-
-
a) T. Weskamp, W. C. Schattenmann, M. Spiegler, W. A. Herrmann, Angew. Chem. 1998, 110, 2631-2633; Angew. Chem. Int. Ed. 1998, 37, 2490-2493; corrigendum:
-
(1998)
Angew. Chem.
, vol.110
, pp. 2631-2633
-
-
Weskamp, T.1
Schattenmann, W.C.2
Spiegler, M.3
Herrmann, W.A.4
-
18
-
-
0032476166
-
-
corrigendum
-
a) T. Weskamp, W. C. Schattenmann, M. Spiegler, W. A. Herrmann, Angew. Chem. 1998, 110, 2631-26tt; Angew. Chem. Int. Ed. 1998, 37, 2490-2493; corrigendum:
-
(1998)
Angew. Chem. Int. Ed.
, vol.37
, pp. 2490-2493
-
-
-
19
-
-
0010278769
-
-
b) T. Weskamp, W. C. Schattenmann, M. Spiegler, W. A. Herrmann, Angew. Chem. 1999, 111, 277; Angew. Chem. Int. Ed. 1999, 38, 262.
-
(1999)
Angew. Chem.
, vol.111
, pp. 277
-
-
Weskamp, T.1
Schattenmann, W.C.2
Spiegler, M.3
Herrmann, W.A.4
-
20
-
-
2142833216
-
-
b) T. Weskamp, W. C. Schattenmann, M. Spiegler, W. A. Herrmann, Angew. Chem. 1999, 111, 277; Angew. Chem. Int. Ed. 1999, 38, 262.
-
(1999)
Angew. Chem. Int. Ed.
, vol.38
, pp. 262
-
-
-
21
-
-
0000201772
-
-
[5c d] See also: U. Frenzel, T. Weskamp, F. J. Kohl, W. C. Schattenmann, O. Nuyken, W. A. Herrmann, J. Organomet. Chem. 1999, 586, 263-265.
-
(1999)
J. Organomet. Chem.
, vol.586
, pp. 263-265
-
-
Frenzel, U.1
Weskamp, T.2
Kohl, F.J.3
Schattenmann, W.C.4
Nuyken, O.5
Herrmann, W.A.6
-
22
-
-
0342835341
-
-
note
-
[5-7] All polymerizations were performed under an atmosphere of nitrogen.
-
-
-
-
23
-
-
0343705769
-
-
note
-
A similar observation is obtained when comparing the ROMP activity of 2 (∼300 equiv COD per hour) and its dimethylvinyl carbene derivative (∼200 equiv COD per hour, catalyst structure not shown).
-
-
-
-
24
-
-
0030994105
-
-
For a comprehensive study on phosphane effects in ruthenium-catalyzed olefin metathesis, see: E. L. Dias, S. T. Nguyen, R. H. Grubbs, J. Am. Chem. Soc. 1997, 119, 3887-3897.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 3887-3897
-
-
Dias, E.L.1
Nguyen, S.T.2
Grubbs, R.H.3
-
25
-
-
58149326227
-
-
For examples of polymerizing low-strain cyclic olefins using complex 1, see: P. Dounis, W. J. Feast, A. M. Kenwright, Polymer 1995, 36, 2787-2796.
-
(1995)
Polymer
, vol.36
, pp. 2787-2796
-
-
Dounis, P.1
Feast, W.J.2
Kenwright, A.M.3
-
26
-
-
0000812356
-
-
Polymers of this type have been prepared by using 2, see: M. A. Hilimyer, W. R. Laredo, R. H. Grubbs, Macromolecules 1995, 28, 6311-6316.
-
(1995)
Macromolecules
, vol.28
, pp. 6311-6316
-
-
Hilimyer, M.A.1
Laredo, W.R.2
Grubbs, R.H.3
-
27
-
-
0006496665
-
-
Other functionalized cyclooctenes have been polymerized by using a cyclometalated aryloxy(chloro)neopentylidenenetungsten complex, see: a) J.-L. Couturier, C. Paillet, M. Leconte, J.-M. Basset, K. Weiss, Angew. Chem. 1992, 104, 622-624; Angew. Chem. Int. Ed. Engl. 1992, 31, 628-631;
-
(1992)
Angew. Chem.
, vol.104
, pp. 622-624
-
-
Couturier, J.-L.1
Paillet, C.2
Leconte, M.3
Basset, J.-M.4
Weiss, K.5
-
28
-
-
33748609335
-
-
Other functionalized cyclooctenes have been polymerized by using a cyclometalated aryloxy(chloro)neopentylidenenetungsten complex, see: a) J.-L. Couturier, C. Paillet, M. Leconte, J.-M. Basset, K. Weiss, Angew. Chem. 1992, 104, 622-624; Angew. Chem. Int. Ed. Engl. 1992, 31, 628-631;
-
(1992)
Angew. Chem. Int. Ed. Engl.
, vol.31
, pp. 628-631
-
-
-
29
-
-
33748225790
-
-
b) J.-L. Couturier, K. Tanaka, M. Leconte, J.-M. Basset, J. Ollivier, Angew. Chem. 1993, 105, 99; Angew. Chem. Int. Ed. Engl. 1993, 32, 112-115.
-
(1993)
Angew. Chem.
, vol.105
, pp. 99
-
-
Couturier, J.-L.1
Tanaka, K.2
Leconte, M.3
Basset, J.-M.4
Ollivier, J.5
-
30
-
-
33748225790
-
-
b) J.-L. Couturier, K. Tanaka, M. Leconte, J.-M. Basset, J. Ollivier, Angew. Chem. 1993, 105, 99; Angew. Chem. Int. Ed. Engl. 1993, 32, 112-115.
-
(1993)
Angew. Chem. Int. Ed. Engl.
, vol.32
, pp. 112-115
-
-
-
32
-
-
0031078006
-
-
b) M. A. Hillmyer, S. T. Nguyen, R. H. Grubbs, Macromolecules 1997, 30, 718 -721.
-
(1997)
Macromolecules
, vol.30
, pp. 718-721
-
-
Hillmyer, M.A.1
Nguyen, S.T.2
Grubbs, R.H.3
-
34
-
-
0027650258
-
-
3, see: M. B. France, R. H. Grubbs, D. V. McGrath, R. A. Paciello, Macromolecules 1993, 26, 4742-4747.
-
(1993)
Macromolecules
, vol.26
, pp. 4742-4747
-
-
France, M.B.1
Grubbs, R.H.2
McGrath, D.V.3
Paciello, R.A.4
-
35
-
-
0028518323
-
-
a) T. Viswanathan, F. Gomez, K. B. Wagener, J. Polym. Sci. Polym. Chem. 1994, 32, 2469-2477;
-
(1994)
J. Polym. Sci. Polym. Chem.
, vol.32
, pp. 2469-2477
-
-
Viswanathan, T.1
Gomez, F.2
Wagener, K.B.3
-
36
-
-
0026119520
-
-
b) H. Cramail, M. Fontanille, A. Soum, J. Mol. Catal. 1991, 65, 193-203.
-
(1991)
J. Mol. Catal.
, vol.65
, pp. 193-203
-
-
Cramail, H.1
Fontanille, M.2
Soum, A.3
-
37
-
-
0025460699
-
-
a) W. E. Crowe, J. P. Mitchell, V. C. Gibson, R. R. Schrock, Maccromolecules 1990, 23, 3534-3536;
-
(1990)
Maccromolecules
, vol.23
, pp. 3534-3536
-
-
Crowe, W.E.1
Mitchell, J.P.2
Gibson, V.C.3
Schrock, R.R.4
-
39
-
-
0343270216
-
-
note
-
The 1,5-dimethyl-1,5-cyclooctadiene (6) employed in this study contained 1,6-dimethyl-1,5-cyclooctadiene (20%) as an inseparable mixture.
-
-
-
-
40
-
-
0343270215
-
-
note
-
[25] We believe that if pure 6 was polymerized, the poly(isoprene) obtained would have perfectly alternating head-to-tail microstructure, since trisubstituted alkylidenes have not been observed to form. Thus, a perfectly alternating ethylene-propylene would be obtained after hydrogenation.
-
-
-
|