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(a) Sanford, M. S.; Love, J. A.; Grubbs, R. H. J. Am. Chem. Soc. 2001, 123, 6543.
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Anderson, D. R.; Hickstein, D. D.; O'Leary, D. J.; Grubbs, R. H. J. Am. Chem. Soc. 2006, 128, 8386.
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Tallarico, J. A.; Bonitatebus, P. J., Jr.; Snapper, M. L. J. Am. Chem. Soc. 1997, 119, 7157.
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24
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41549101900
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IH NMR spectra of 3.
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IH NMR spectra of 3.
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26
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41549094818
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3 unit.
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3 unit.
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27
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0001379732
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(a) Wallace, K. C.; Liu, A. H.; Dewan, J. C.; Schrock, R. R. J. Am. Chem. Soc. 1988, 110, 4964.
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Wallace, K.C.1
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Schrock, R.R.4
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30
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41549098569
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CC between the α carbons is unresolved in these spectra.
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CC between the α carbons is unresolved in these spectra.
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32
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41549143500
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Webb, C. A, Ed
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(a) Wray, V.; Hansen, P. E. (Webb, C. A., Ed.) Ann. Rep. NMR Spectrosc. 1981, 32, 789.
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Wray, V.1
Hansen, P.E.2
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34
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41549136363
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Even in cyclopropane, where the C-C bonds have high p-character, the coupling constant is 12.4 Hz: Hesse, M.; Meier, H.; Zeeh, B. Spectroscopic Methods in Organic Chemistry; Georg Thieme Verlag: New York, 1997.
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(c) Even in cyclopropane, where the C-C bonds have high p-character, the coupling constant is 12.4 Hz: Hesse, M.; Meier, H.; Zeeh, B. Spectroscopic Methods in Organic Chemistry; Georg Thieme Verlag: New York, 1997.
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37
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28444486339
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Harvey, B. G.; Mayne, C. L.; Arif, A. M.; Ernst, R. D. J. Am. Chem. Soc. 2005, 127, 16426.
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Harvey, B.G.1
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38
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1642280467
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Some computational studies support this finding: (a) Adlhart, C.; Chen, P. J. Am. Chem. Soc. 2004, 126, 3496.
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Some computational studies support this finding: (a) Adlhart, C.; Chen, P. J. Am. Chem. Soc. 2004, 126, 3496.
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40
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34249094124
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3 derivatives of Grubbs catalysts, see: Bolton, S. L.; Williams, J. E.; Sponsler, M. B. Organometallics 2007, 26, 2485.
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3 derivatives of Grubbs catalysts, see: Bolton, S. L.; Williams, J. E.; Sponsler, M. B. Organometallics 2007, 26, 2485.
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41
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36448940883
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Related species have recently been detected but not thoroughly characterized: P'Pool, S. J.; Schanz, H.-J. J. Am. Chem. Soc. 2007, 129, 14200.
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Related species have recently been detected but not thoroughly characterized: P'Pool, S. J.; Schanz, H.-J. J. Am. Chem. Soc. 2007, 129, 14200.
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42
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16244406254
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PH in Grubbs-type ruthenium carbenes has been noted: (a) Lehman, S. E., Jr.; Wagener, K. B. Organometallics 2005, 24, 1477.
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PH in Grubbs-type ruthenium carbenes has been noted: (a) Lehman, S. E., Jr.; Wagener, K. B. Organometallics 2005, 24, 1477.
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43
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84989561615
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(b) Nguyen, S. T.; Grubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1993, 115, 9858-9859.
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0001698392
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(c) Wu, Z.; Nguyen, S. T.; Grubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1995, 117, 5503-5511.
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45
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0043194171
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Chatterjee, A. K.; Choi, T.-L.; Sanders, D. P.; Grubbs, R. H. J. Am. Chem. Soc. 2003, 125, 11360.
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Chatterjee, A.K.1
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Grubbs, R.H.4
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46
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0000985125
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Deactivation of ruthenium-based olefin metathesis catalysts via dimerization has been previously observed: (a) Amoroso, D, Yap, G. P. A, Fogg, D. E. Organometallics 2002, 21, 3335
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Deactivation of ruthenium-based olefin metathesis catalysts via dimerization has been previously observed: (a) Amoroso, D.; Yap, G. P. A.; Fogg, D. E. Organometallics 2002, 21, 3335.
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47
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26644455050
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(b) Drouin, S. D.; Monfette, S.; Amoroso, D.; Yap, G. P. A., Fogg, D. E. Organometallics 2005, 24, 4721.
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Drouin, S.D.1
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Yap, G.P.A.4
Fogg, D.E.5
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48
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41549094383
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Note that only 1 equiv of the acenaphthylene substrate opens; we do not observe ROMP of this substrate under any conditions explored.
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Note that only 1 equiv of the acenaphthylene substrate opens; we do not observe ROMP of this substrate under any conditions explored.
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