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1
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28244440935
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For recent reviews on ring closing alkene metathesis, see:
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For recent reviews on ring closing alkene metathesis, see:. Armstrong S.K. J. Chem. Soc., Perkin Trans. 1 (1998) 371
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(1998)
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Armstrong, S.K.1
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3
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33745391920
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M.L. Snapper, A.H. Hoveyda (Eds.), Tetrahedron Symposium 55, 1999, p. 8141.
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4
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33745353966
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A. Furstner (Ed.), Top. Organomet. Chem. 1 (1998).
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12
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0033556066
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For double RCM approaches to fused bicyclic compounds:
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For double RCM approaches to fused bicyclic compounds:. Lautens M., and Hughes G. Angew. Chem., Int. Ed. Engl. 38 (1999) 129
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(1999)
Angew. Chem., Int. Ed. Engl.
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Lautens, M.1
Hughes, G.2
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13
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0034697870
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Bassingdale M.J., Edwards A.S., Hamley P., Adams H., and Harrity J.P.A. Chem. Commun. (2000) 1035
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Chem. Commun.
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Bassingdale, M.J.1
Edwards, A.S.2
Hamley, P.3
Adams, H.4
Harrity, J.P.A.5
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19
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0034681742
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Wallace D.J., Cowden C.J., Kennedy D.J., Ashwood M.S., Cottrell I.F., and Dolling U.-H. Tetrahedron Lett. 41 (2000) 2027
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(2000)
Tetrahedron Lett.
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Wallace, D.J.1
Cowden, C.J.2
Kennedy, D.J.3
Ashwood, M.S.4
Cottrell, I.F.5
Dolling, U.-H.6
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23
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0035107363
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Wallace D.J., Bulger P.G., Kennedy D.J., Ashwood M.S., Cottrell I.F., and Dolling U.-H. Synlett (2001) 357
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(2001)
Synlett
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Wallace, D.J.1
Bulger, P.G.2
Kennedy, D.J.3
Ashwood, M.S.4
Cottrell, I.F.5
Dolling, U.-H.6
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25
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0037190847
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Wybrow R.A.J., Johnson L.A., Auffray B., Moran W.J., Adams H., and Harrity J.P.A. Tetrahedron Lett. 43 (2002) 7851
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(2002)
Tetrahedron Lett.
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Wybrow, R.A.J.1
Johnson, L.A.2
Auffray, B.3
Moran, W.J.4
Adams, H.5
Harrity, J.P.A.6
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30
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4444301978
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Wybrow R.A.J., Edwards A.S., Stevenson N.G., Adams H., Johnstone C., and Harrity J.P.A. Tetrahedron 60 (2004) 8869
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(2004)
Tetrahedron
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Wybrow, R.A.J.1
Edwards, A.S.2
Stevenson, N.G.3
Adams, H.4
Johnstone, C.5
Harrity, J.P.A.6
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38
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25844469499
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Clark J.S., Kimber M.C., Robertson J., McErlean C.S.P., and Wilson C. Angew. Chem. Int. Ed. Eng. 44 (2005) 6157
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Clark, J.S.1
Kimber, M.C.2
Robertson, J.3
McErlean, C.S.P.4
Wilson, C.5
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39
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0029884246
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For some examples of ring opening, double ring closing strategies see:
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For some examples of ring opening, double ring closing strategies see:. Zuercher W.J., Hashimoto M., and Grubbs R.H. J. Am. Chem. Soc. 118 (1996) 6634
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(1996)
J. Am. Chem. Soc.
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Zuercher, W.J.1
Hashimoto, M.2
Grubbs, R.H.3
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46
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0035826378
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Wallace D.J., Goodman J.M., Kennedy D.J., Davies A.J., Cowden C.J., Ashwood M.S., Cottrell I.F., Dolling U.-H., and Reider P.J. Org. Lett. 3 (2001) 671
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(2001)
Org. Lett.
, vol.3
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Wallace, D.J.1
Goodman, J.M.2
Kennedy, D.J.3
Davies, A.J.4
Cowden, C.J.5
Ashwood, M.S.6
Cottrell, I.F.7
Dolling, U.-H.8
Reider, P.J.9
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48
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0037154769
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Maligres P.E., Waters M.M., Lee J., Reamer R.A., Askin D., Ashwood M.S., and Cameron M. J. Org. Chem. 67 (2002) 1093
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J. Org. Chem.
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Maligres, P.E.1
Waters, M.M.2
Lee, J.3
Reamer, R.A.4
Askin, D.5
Ashwood, M.S.6
Cameron, M.7
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54
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33745387005
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In this paper we use the term "first generation catalyst" to cover those lacking the dihydroimidazole ligand, e.g. (6) and "second generation catalyst" to cover those with the dihydroimidazole ligand, e.g. (7).
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57
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33745422141
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Any reaction through path A would generate the same five membered rings as previously isolated, i.e. (4a) and (4b).
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58
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2942678732
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These reactions typically stalled at 50% conversion, which may be due to decomposition of the catalyst via the ruthenium methylidene which could be accelerated by the ethylene atmosphere, see:
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These reactions typically stalled at 50% conversion, which may be due to decomposition of the catalyst via the ruthenium methylidene which could be accelerated by the ethylene atmosphere, see:. Hong S.H., Day M.W., and Grubbs R.H. J. Am. Chem. Soc. 126 (2004) 7414
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(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 7414
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Hong, S.H.1
Day, M.W.2
Grubbs, R.H.3
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59
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7744223654
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van Rensburg W.J., Steynberg P.J., Meyer W.H., Kirt M., and Forman G.S. J. Am. Chem. Soc. 126 (2004) 14332
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(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 14332
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van Rensburg, W.J.1
Steynberg, P.J.2
Meyer, W.H.3
Kirt, M.4
Forman, G.S.5
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60
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33745419034
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A.J. Robinson, Contributed lecture at International Symposium on Olefin Metathesis and Related Chemistry, Poznan, Poland, August 2005.
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In the absence of further catalyst activation this reaction typically stalled at 50% conversion.
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62
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4143062538
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Relay RCM is an alternative method to control the order of ring closing events, see:
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Relay RCM is an alternative method to control the order of ring closing events, see:. Hoye T.R., Jeffrey C.S., Tennakoon M.A., Wang J., and Zhau H. J. Am. Chem. Soc. 126 (2004) 10210
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(2004)
J. Am. Chem. Soc.
, vol.126
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Hoye, T.R.1
Jeffrey, C.S.2
Tennakoon, M.A.3
Wang, J.4
Zhau, H.5
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