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1 1 Ballini, R. and Palmieri, A. (2018). Adv. Synth. Catal. 360: 2240–2266.

2 2 Meyer, V. and Stuber, O. (1872). Ber. Dtsch. Chem. Ges. 5: 203–205.

3 3 Kornblum, N., Larson, H.O., Blackwood, R.K. et al. (1956). J. Am. Chem. Soc. 78: 1497–1501.

4 4 Easton, C.J., Xia, L., Pitt, M.J. et al. (2001). Synthesis: 451–458.

5 5 Alaime, T., Delots, A., Pasquinet, E. et al. (2016). Tetrahedron 72: 1337–1341.

6 6 Ballini, R., Barboni, L., and Giarlo, G. (2004). J. Org. Chem. 69: 6907–6908.

7 7 Ballini, R., Barboni, L., and Palmieri, A. (2008). Green Chem. 10: 1004–1006.

8 8 Sheldon, R.A. (2005). Green Chem. 7: 267–278.

9 9 Chen, J., Spear, S.K., Huddleston, J.G., and Rogers, R.D. (2005). Green Chem. 7: 64–82.

10 10 Palmieri, A., Gabrielli, S., and Ballini, R. (2013). Beilstein J. Org. Chem. 9: 533–536.

11 11 Keinan, E. and Mazur, Y. (1977). J. Org. Chem. 42: 844–847.

12 12 Menger, F.M. and Lee, C. (1981). Tetrahedron Lett. 22: 1655–1656.

13 13 Kornblum, N., Clutter, R.J., and Jones, W.J. (1956). J. Am. Chem. Soc. 78: 4003–4004.

14 14 Emmons, W.D. (1957). J. Am. Chem. Soc. 79: 5528–5530.

15 15 Gilber, K.E. and Border, W.T. (1979). J. Org. Chem. 44: 659–661.

16 16 Murray, R.W., Rajadhaksha, S.N., and Mohan, L. (1989). J. Org. Chem. 54: 5783–5788.

17 17 Irfan, M., Glsnov, T.N., and Kappe, C.O. (2011). Org. Lett. 13: 984–987.

18 18 Harel, T. and Rozen, S. (2007). J. Org. Chem. 72: 6500–6503.

19 19 McPake, C.B., Murray, C.B., and Sandford, G. (2012). ChemSusChem 5: 312–319.

20 20 Krohn, K. and Küpke, J. (1998). Eur. J. Org. Chem.: 679–682.

21 21 Nef, J.U. (1894). Liebigs Ann. Chem. 280: 264–268.

22 22 Emmons, W.D. and Pagano, A.S. (1955). J. Am. Chem. Soc. 77: 4557–4559.

23 23 Ballini, R., Marcantoni, E., and Petrini, M. (1992). Tetrahedron Lett. 33: 4835–4838.

24 24 Olah, G.A., Ramaiah, P., Lee, C.S., and Prakash, G.K.S. (1992). Synlett: 337–339.

25 25 Ballistreri, F.P., Barbuzzi, E., Tomaselli, G.A., and Toscano, R.M. (1996). Synlett: 1093–1094.

26 26 Rozen, S. and Carmeli, M. (2003). J. Am. Chem. Soc. 125: 8118–8119.

27 27 Barret, G.M. and Graboski, G.G. (1986). Chem. Rev. 86: 751–762.

28 28 Kabalka, G.W., Guind, L.H.M., and Varma, R.S. (1990). Tetrahedron 46: 7443–7457.

29 29 Sinhababu, A.K. and Borchard, R.T. (1983). Tetrahedron Lett. 24: 227–230.

30 30 Gupta, A., Haque, A., and Vankar, Y.D. (1996). Chem. Commun.: 1653–1654.

31 31 Kawai, Y., Inaba, Y., Hayashi, M., and Tokitoh, N. (2001). Tetrahedron Lett. 42: 3367–3368.

32 32 Kawai, Y., Inaba, Y., Hayashi, M., and Tokitoh, N. (2001). Tetrahedron: Asymmetry 12: 309–318.

33 33 Czekelius, C. and Carreira, E.M. (2003). Angew. Chem. Int. Ed. 42: 4793–4795.

34 34 Czekelius, C. and Carreira, E.M. (2004). Org. Lett. 6: 4575–4577.

35 35 Soltani, O., Ariger, M.A., and Carreira, E.M. (2009). Org. Lett. 11: 4196–4198.

36 36 Fryszkowska, A., Fisher, K., Gardiner, J.M., and Stephens, G.M. (2008). J. Org. Chem. 73: 4295–4298.

37 37 Wollenberg, R.H. and Miller, S.J. (1978). Tetrahedron Lett. 19: 3219–3222.

38 38 Markofsky, S.B. (1999). Ullmann’s Encyclopedia of Industrial Organic Chemicals, vol. 6 (eds. B. Elvers and S. Hawkins), 3487–3501. Weinheim: Wiley-VCH.

39 39 Sakagichi, S., Nishiwali, Y., Kitamura, T., and Ishii, Y. (2001). Angew. Chem. Int. Ed. 40: 222–224.

40 40 Walvoord, R.R., Berritt, S., and Kozlowski, M.C. (2012). Org. Lett. 14: 4086–4089.

41 41 Vogl, E.M. and Buchwald, S.L. (2002). J. Org. Chem. 67: 106–111.

42 42 Trost, B.M. and Surivet, J.-P. (2000). Angew. Chem. Int. Ed. 39: 3122–3124.

43 43 Deardoff, D.R., Savin, K.A., Justman, C.J. et al. (1996). J. Org. Chem. 61: 361–362.

44 44 Padilla-Salinas, R., Walvoord, R.R., Tcyrulnikov, S., and Kozlowski, M.C. (2013). Org. Lett. 15: 3966–3969.