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1
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84902415597
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(a) S.T. Nguyen, L.K. Johnson, R.H. Grubbs, J.W. Ziller, J. Am. Chem. Soc. 114 (1992) 3974.
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(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 3974
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Nguyen, S.T.1
Johnson, L.K.2
Grubbs, R.H.3
Ziller, J.W.4
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2
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33746236970
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(b) P. Schwab, M.B. France, J.W. Ziller, R.H. Grubbs, Angew. Chem. Int. Ed. Engl. 34 (1995) 2039.
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(1995)
Angew. Chem. Int. Ed. Engl.
, vol.34
, pp. 2039
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Schwab, P.1
France, M.B.2
Ziller, J.W.3
Grubbs, R.H.4
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8
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0034639441
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(e) H.E. Blackwell, D.J. O'Leary, A.K. Chatterjee, R.A. Washenfelder, D.A. Bussmann, R.H. Grubbs, J. Am. Chem. Soc. 122 (2000) 58.
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(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 58
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Blackwell, H.E.1
O'Leary, D.J.2
Chatterjee, A.K.3
Washenfelder, R.A.4
Bussmann, D.A.5
Grubbs, R.H.6
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9
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0343128903
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(a) A. Mühlebach, P.A. van der Schaaf, A. Hafner, F. Setiabudi, J. Mol. Catal. A: Chem. 132 (1998) 181.
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(1998)
J. Mol. Catal. A: Chem.
, vol.132
, pp. 181
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Mühlebach, A.1
Van Der Schaaf, P.A.2
Hafner, A.3
Setiabudi, F.4
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14
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0347982964
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Patent WO 97/20865
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A patent has been filed using triphenyl phosphine as gel modification agent: C.S. Woodson Jr., R.H. Grubbs, Patent WO 97/20865.
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Woodson C.S., Jr.1
Grubbs, R.H.2
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15
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0001698392
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3 containing hetero atom substituted ruthenium carbenes are inactive in olefin metathesis reactions: Z. Wu, S.T. Nguyen, R.H. Grubbs, J.W. Ziller, J. Am. Chem. Soc. 117 (1995) 5503.
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(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 5503
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Wu, Z.1
Nguyen, S.T.2
Grubbs, R.H.3
Ziller, J.W.4
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18
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0032538017
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(a) J.N. Coalter III, G.J. Spivak, H. Gerard, E. Clot, E.R. Davidson, O. Eisenstein, K.G. Caulton, J. Am. Chem. Soc. 120 (1998) 9388.
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(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 9388
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Coalter J.N. III1
Spivak, G.J.2
Gerard, H.3
Clot, E.4
Davidson, E.R.5
Eisenstein, O.6
Caulton, K.G.7
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19
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33646142047
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(b) T.E. Wilhelm, T.R. Beldarrain, S.N. Brown, R.H. Grubbs, Organometallics 16 (1997) 3867.
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(1997)
Organometallics
, vol.16
, pp. 3867
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Wilhelm, T.E.1
Beldarrain, T.R.2
Brown, S.N.3
Grubbs, R.H.4
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21
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0000851147
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(d) C. Grünwald, O. Gevert, J. Wolf, P. Gonzalez-Herrero, H. Werner, Organometallics 15 (1996) 1960.
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(1996)
Organometallics
, vol.15
, pp. 1960
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Grünwald, C.1
Gevert, O.2
Wolf, J.3
Gonzalez-Herrero, P.4
Werner, H.5
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22
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0344541773
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(e) J. Wolf, W. Stüer, C. Grünwald, H. Werner, P. Schwab, M. Schulz, Angew. Chem. Int. Ed. Engl. 37 (1998) 1124.
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(1998)
Angew. Chem. Int. Ed. Engl.
, vol.37
, pp. 1124
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Wolf, J.1
Stüer, W.2
Grünwald, C.3
Werner, H.4
Schwab, P.5
Schulz, M.6
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28
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0001645448
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Another approach of an intramolecularly coordinating ligand using a bidentate Schiff-base ligand has been published recently: S. Chang, L. Jones II, C. Wang, L.M. Henling, R.H. Grubbs, Organometallics 17 (1998) 3460.
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(1998)
Organometallics
, vol.17
, pp. 3460
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Chang, S.1
Jones L. II2
Wang, C.3
Henling, L.M.4
Grubbs, R.H.5
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29
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0347982961
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Patent US 3,499,039
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H.J. Lorenz, A.R. Zintl, V. Franzen, Patent US 3,499,039.
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Lorenz, H.J.1
Zintl, A.R.2
Franzen, V.3
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36
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0346722197
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(b) K. Takahashi, K. Konishi, M. Ushio, M. Takaki, R. Asami, J. Organomet. Chem. 50 (1973) 1.
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(1973)
J. Organomet. Chem.
, vol.50
, pp. 1
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Takahashi, K.1
Konishi, K.2
Ushio, M.3
Takaki, M.4
Asami, R.5
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37
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0002819513
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(c) E. Kaiser, G.J. Bartling, W.R. Thomas, S.B. Nichols, D.R. Nash, J. Org. Chem. 38 (1973) 71.
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(1973)
J. Org. Chem.
, vol.38
, pp. 71
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Kaiser, E.1
Bartling, G.J.2
Thomas, W.R.3
Nichols, S.B.4
Nash, D.R.5
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38
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0347352660
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note
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The yield of the synthesis can be increased when some radical scavenger, like 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxy radical (4-hydroxy-TEMPO = PROSTAB™ 5198 of Ciba Specialty Chemicals), is added to the crude product before distillation to prevent polymerization. It is advisable to add also some stabilizer when the product has to be stored for longer periods of time.
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40
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0004150157
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Universität Göttingen, Göttingen, Germany
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G.M. Sheldrick, SHELXL-97, Universität Göttingen, Göttingen, Germany, 1999.
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(1999)
SHELXL-97
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Sheldrick, G.M.1
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