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(a) Nguyen, S. T.; Grubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1993, 115, 9858.
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(b) Schwab, P.; Grubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1996, 118, 100.
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Schwab, P.1
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3
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0032580376
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For recent reviews see the following for leading references: (a) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413.
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(1998)
Tetrahedron
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Grubbs, R.H.1
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5
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0030771019
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(c) Schuster, M.; Blechert, S. Angew. Chem., Int. Ed. Engl. 1997, 36, 2036.
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Schuster, M.1
Blechert, S.2
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8
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0001101871
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For a detailed study on the effects of substitution on RCM, see: Kirkland, T. A.; Grubbs, R. H. J. Org. Chem. 1997, 62, 7310.
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(1997)
J. Org. Chem.
, vol.62
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Kirkland, T.A.1
Grubbs, R.H.2
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9
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0030660076
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Review on N-heterocyclic carbenes: Herrmann, W. A.; Köcher, C. Angew. Chem., Int. Ed. Engl. 1997, 36, 2162.
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(1997)
Angew. Chem., Int. Ed. Engl.
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, pp. 2162
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Herrmann, W.A.1
Köcher, C.2
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10
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0033620417
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For R = mesityl see ref 6 and the following paper: Huang, J.; Stevens, E. D.; Nolan, S. P.; Petersen, 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
Petersen, J.L.4
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11
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0033582991
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For "saturated" carbene analogues thereof see
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For R = mesityl see ref 5 and the following paper: (a) Scholl, M.; Trnka, T. M.; Morgan, J. P.; Grubbs, R. H. Tetrahedron Lett. 1999, 40, 2247. For "saturated" carbene analogues thereof see:
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Tetrahedron Lett.
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Scholl, M.1
Trnka, T.M.2
Morgan, J.P.3
Grubbs, R.H.4
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12
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0033598258
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(b) Scholl, M.; Ding, S.; Lee, C. W.; Grubbs, R. H. Org. Lett. 1999, 1, 953.
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Org. Lett.
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Scholl, M.1
Ding, S.2
Lee, C.W.3
Grubbs, R.H.4
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14
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0033603294
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For R = isopropyl, cyclohexyl, -CHMePh, -CHMe(naphthyl), and mesityl, see: (a) Ackermann, L.; Fürstner, A.; Weskamp, T.; Kohl, F. J.; Herrmann, W. A. Tetrahedron Lett. 1999, 40, 4787.
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Tetrahedron Lett.
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Ackermann, L.1
Fürstner, A.2
Weskamp, T.3
Kohl, F.J.4
Herrmann, W.A.5
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15
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0001587279
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(b) Weskamp, T.; Kohl, F. J.; Gleich, D.; Herrmann, W. A. Angew. Chem. 1999, 111, 2573.
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Weskamp, T.1
Kohl, F.J.2
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Herrmann, W.A.4
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17
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0001077422
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(a) Schrock, R. R.; Murdzek, J. S.; Bazan, G. C.; Robbins, J.; DiMare, M.; O'Regan, M. J. Am. Chem. Soc. 1990, 112, 3875.
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Schrock, R.R.1
Murdzek, J.S.2
Bazan, G.C.3
Robbins, J.4
Dimare, M.5
O'Regan, M.6
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19
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0343608397
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note
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Note that the same reaction catalyzed by 1 (5 mol %) requires ≥24 h!
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20
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0030786787
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In some cases, alkene isomerizations have also been observed with more conventional catalysts, cf.: (a) Joe, D.; Overman, L. E. Tetrahedron Lett. 1997, 38, 8635.
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(1997)
Tetrahedron Lett.
, vol.38
, pp. 8635
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Joe, D.1
Overman, L.E.2
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21
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0028428067
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(b) Marciniec, B.; Foltynowicz, Z.; Lewandowski, M. J. Mol. Catal. 1994, 90, 125.
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Marciniec, B.1
Foltynowicz, Z.2
Lewandowski, M.3
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22
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0343471448
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(c) Thorn-Csanyi, E.; Dehmel, J.; Luginsland, H.-D.; Zilles, J. U. J. Mol. Catal. A 1997, 115, 29.
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J. Mol. Catal. A
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Thorn-Csanyi, E.1
Dehmel, J.2
Luginsland, H.-D.3
Zilles, J.U.4
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26
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0038590297
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(d) Fürstner, A., Grabowski, J.; Lehmann, C. W. J. Org. Chem. 1999, 64, 8275.
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Fürstner, A.1
Grabowski, J.2
Lehmann, C.W.3
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30
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0033515494
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(h) Fürstner, A.; Gastner, T.; Weintritt, H. J. Org. Chem. 1999, 64, 2361.
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J. Org. Chem.
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Fürstner, A.1
Gastner, T.2
Weintritt, H.3
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31
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0033516492
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(i) Fürstner, A.; Seidel, G.; Kindler, N. Tetrahedron 1999, 55, 8215.
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(1999)
Tetrahedron
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Fürstner, A.1
Seidel, G.2
Kindler, N.3
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33
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0342738471
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2OH is the diphenylallenylidene complex depicted in Scheme 3, cf.: Harlow, K. J.; Hill, A. F.; Winton-Ely, J. D. E. T. J. Chem. Soc., Dalton Trans. 1999, 285. More detailed studies, however, have shown that the stable product formed in this reaction is the rearranged product, i.e., the indenylidene ruthenium complex 10, cf.: Hill, A. F.; Fürstner, A.; Liebl, M.; Mynott, R.; Gabor, B., Jafarpour, L.; Nolan, S. P. Manuscript in preparation.
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J. Chem. Soc., Dalton Trans.
, vol.285
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Harlow, K.J.1
Hill, A.F.2
Winton-Ely, J.D.E.T.3
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34
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0342303340
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Manuscript in preparation
-
2OH is the diphenylallenylidene complex depicted in Scheme 3, cf.: Harlow, K. J.; Hill, A. F.; Winton-Ely, J. D. E. T. J. Chem. Soc., Dalton Trans. 1999, 285. More detailed studies, however, have shown that the stable product formed in this reaction is the rearranged product, i.e., the indenylidene ruthenium complex 10, cf.: Hill, A. F.; Fürstner, A.; Liebl, M.; Mynott, R.; Gabor, B., Jafarpour, L.; Nolan, S. P. Manuscript in preparation.
-
-
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Hill, A.F.1
Fürstner, A.2
Liebl, M.3
Mynott, R.4
Gabor, B.5
Jafarpour, L.6
Nolan, S.P.7
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35
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0000713963
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(b) The preparation and X-ray structure of 3b are described in: Jafarpour, L.; Schanz, H.-J.; Stevens, E. D.; Nolan, S. P. Organometallics 1999, 18, 5416.
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(1999)
Organometallics
, vol.18
, pp. 5416
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Jafarpour, L.1
Schanz, H.-J.2
Stevens, E.D.3
Nolan, S.P.4
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36
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0038023350
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Fürstner, A.; Hill, A. F.; Liebl, M.; Wilton-Ely, J. D. E. T. Chem. Commun. 1999, 601.
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Chem. Commun.
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Fürstner, A.1
Hill, A.F.2
Liebl, M.3
Wilton-Ely, J.D.E.T.4
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37
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78249281266
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Fu, G. C.; Nguyen, S. T.; Grubbs, R. H. J. Am. Chem. Soc. 1993, 115, 9856.
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(1993)
J. Am. Chem. Soc.
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Fu, G.C.1
Nguyen, S.T.2
Grubbs, R.H.3
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38
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0000122520
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Huang, J.; Schanz, H.-J.; Stevens, E. D.; Nolan, S. P. Organometallics 1999, 18, 2370.
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(1999)
Organometallics
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Huang, J.1
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Stevens, E.D.3
Nolan, S.P.4
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