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Bibliography

1- Calderon N., Chen H.Y, Scott K.W, Tetrahedron Lett, 1967, 34, 3327-3329.

2 - Schrock R. R., Chem. Rev., 2009, 109, 3211.

3 - Grubbs R. H., Angew. Chem. Int. Ed., 2006, 45, 3760.

4 - Herrison J.L., Chauvin Y., Makromol. Chem., 1971, 141, 161.

5 - Mol J.C.,J.Mol.Cata. A: Chem, 2004, 213, 39-45.

6 - Ivin K. and Mol H., Olefin Metath. and Metathesis polim.

7 - Ivin K.J. and Mol J.C., Academic Press, London, 1997.

8 - Ivin K. J., Mol J. C., Olefin Metathesis and Metathesis Polymerization, Academic Press, San Diego, 1997.

9 - Ivin K. J, Olefin Metathesis, Academic, New York, 1983.

10 - Dragutan V., Balaban A. T, Dimonie M., Olefin Metathesis and Ring-Opening Polymerization of Cyclo-Olefins, 2nd ed., Wiley, New York, 1985.

11 - Schrock R. R., Hoveyda A. H., Angew. Chem. Int. Ed., 2003, 42, 45-92-4633.

12 - Schrock R.R., Chem. Comm., 2005, 2773-2777.

13 - Solans X., Copéret C., Eisenstein O., Organometallics, 2012, 31, 6812-6822.

14 - Poater A., Solans X., Copéret C., Eisenstein O., JACS, 2007, 129, 8207-8216.

15 - Rhers B., Salameh A., Copéret C., Eisenstein O., Schrock R., Organometallics, 2006, 25, 3554-3557.

16 - Solans-Monfort X., Clot E., Copéret C., Eisenstein O., JACS, 2005, 127, 14015- 14025.

17 - Solans X., Copéret C, Eisenstein O., JACS, 2012, 31, 6812-6822.

18 - Poater A., Solans X., Copéret C., Dalton Trans., 2006, 3077-3087.

19 - Solans X., Copéret C., Eisenstein O., J. Am. Chem. Soc., 2010, 132, 7750-7757.

20 - Reithofer M.R. et al., Organometallics, 2013, 32, 2489-2492.

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21 - Gerber L. C. H., Schrock R. R. and Müller P., Organometallics, 2013, 32, 2373-2378.

22 - Townsend M., Schrock R. R. and Hoveyda A. H., J. Am. Chem. Soc., 2012, 134, 11334-11337.

23 - Conley, M. P.; Mougel, V.; Peryshkov, D. V.; Forrest, W. P.; Gajan, D.; Lesage, A.;

Emsley, L.; Copéret, C.; Schrock, R. R. J. Am. Chem. Soc. 2013, 135, 19068-19070.

24 - Conley, M. P.; Forrest, W. P.; Mougel, V.; Copéret, C.; Schrock, R. R. Angew. Chem.

Int. Ed. 2014, 126, 51, 14445-14448.

25 - Solans X., Copéret C., O. Eisenstein, J. Am. Chem. Soc., 2012, 6812-6822.

26 - Mougel V., Copéret C., Chem. Sci., 2014, 5, 2475-2481.

27 - Note that thiolate ligands have shown improved Z-selectivities in Ru-based catalyst, see: (a) Occhipinti, G.; Hansen, F. R.; Törnroos, K. W.; Jensen, V. R. J. Am. Chem. Soc.

2013, 135, 3331. (b) Khan, R. K. M.; Torker, S.; Hoveyda, A. H. J. Am. Chem. Soc. 2013,

135, 10258. (c) Koh, M. J.; Khan, R. K. M.; Torker, S.; Hoveyda, A. H. Angewandte Chemie International Edition 2014, 53, 1968.

28 - Townsend, E. M.; Hyvl, J.; Forrest, W. P.; Schrock, R. R.; Müller, P.; Hoveyda, A. H.

Organometallics 2014, 33, 5334.

29 - Coperet, C.; Mougel, V.; Frater, G. E.; Varga J.; Hegedus, C. Immobilized Tungsten Catalysts and Use Thereof in Olefin Metathesis. Eur. Pat. Appl. 13003540 2013.

30 - Coperet, C.; Mougel, V.; Frater, G. E.; Varga J.; Hegedus, C. ́ 253 Robe, E. Use of Immobilized Molybdenum and Tungsten containing 254 Catalysts in Olefin Cross metathesis. Eur. Pat. Appl. 109914P771.

31 - Florian Allouche, Master thesis, ETH Zürich, 2013.

32 - Peryshkov, D. V.; Schrock, R. R. Organometallics 2012, 31, 7278.

33 - Peryshkov, D. V.; Schrock, R. R.; Takase, M. K.; Muller, P.; Hoveyda, A. H. J. Am.

Chem. Soc. 2011, 133, 20754.

34 - Dolci S., Marchetti F., Pampaloni G. and Zacchini S., Dalton Trans., 2013, 42, 5635.

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35 - Mirza Z. A. et al, J. Chem. Pharm. Res., 2014, 6, 706-710.

36 - Wengrovius J. H. and Schrock R. R., Organometallics, 1982, 1, 148-155.

37 - Kagan, Gerald; Li, Weibin; Hopson, Russell; Williard, Paul G. Organic Letters, 2009 , 11, 21, 4818 – 4821.

38 - O'Donoghue, M. B.; Schrock, R. R.; LaPointe, A. M.; Davis, W. M. Organometallics 1996, 15, 1334.

39 - L. K. Johnson, S. C. Virgil, R. H. Grubbs, J. W. Ziller, J. Am. Chem. SOC. 1990, 112, 5384.

40 - B. H. Lipshutz and P. A. Blomgren, Organic Letters, 2001, vol. 3, 12, 1869-1871.

41 - D. Peryshkov, R. Shrock et al., J. Am. Chem. Soc., 2011, 133, 2754-20757.

42 - H. Jacobsen, H. Berke et al., Organometallics, 1999, 18, 1724-1735.

43 - Solans-Monfort, X.; Coperet, C.; Eisenstein, O. J. Am. Chem. Soc., 2010, 132, 7750.

44 - Solans-Monfort, X.; Copéret, C.; Eisenstein, O. Organometallics, 2012, 31, 6812.

45 - Conley, M. P.; Mougel, V.; Peryshkov, D. V.; Forrest, W. P.; Gajan, D.; Lesage, A.;

Emsley, L.; Copéret, C.; Schrock, R. R. J. Am. Chem. Soc. 2013, 135, 19068.

46 - Samantaray, M. K.; Alauzun, J.; Gajan, D.; Kavitake, S.; Mehdi, A.; Veyre, L.; Lelli, M.;

Lesage, A.; Emsley, L.; Copéret, C.; Thieuleux, C. J. Am. Chem. Soc. 2013, 135, 3193.

47 - In agreement with Schrock and coworkers who reported very low conversion of 18%

after 24h at 1 mol% loading in 1-octene metathesis (see reference 33 for details).

48 - Blanc, F.; Berthoud, R.; Copéret, C.; Lesage, A.; Emsley, L.; Singh, R.; Kreickmann, T.; Schrock, R. R. Proc. Nat. Acad. Sci. U.S.A. 2008, 105, 12123.

49 - Mougel, V.; Coperet, C. Chem. Sci. 2014, 5, 2475.

50 - J. Elison, K. Ruhlandt-Senge, P. Power, Angew. Chem. Int. Ed., 1994, 33, 1178.

51 - A. J. Rossini, A. Zagdoun, M. Lelli, D. Gajan, C. Copéret, A. Lesage, L. Emsley et al., Chem. Sci., 2012, 3, 108.

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52 - Note: The XRD measurement and structure refinement were performed by Dr. Victor Mougel, ETH Zurich).

Riferimenti

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