Acknowledgments The authors thank Re ´gion Rho ˆne-Alpes (ARC Sante ´) and Fondation Pierre
Potier pour le De ´veloppement de la Chimie des Substances Naturelles et ses Applications for
financial support.
References
1. Dick AR, Sanford MS (2006) Tetrahedron 62:2439
2. Jazzar R, Hitce J, Renaudat A, Sofack-Kreutzer J, Baudoin O (2010) Chem Eur J 16:2654
3. Baudoin O (2011) Chem Soc Rev 40:4902
4. Li H, Li BJ, Shi ZJ (2011) Catal Sci Technol 1:191
5. Dastbaravardeh N, Christakakou M, Haider M, Schnu ¨rch M (2014) Synthesis 46:1421
6. McMurray L, O’Hara F, Gaunt MJ (2011) Chem Soc Rev 40:1885
7. Gutekunst WR, Baran PS (2011) Chem Soc Rev 40:1976
8. Yamaguchi J, Yamaguchi AD, Itami K (2012) Angew Chem Int Ed 51:8960
9. Johnson JA, Sames D (2000) J Am Chem Soc 122:6321
10. Holtcamp MW, Henling LM, Day MW, Labinger JA, Bercaw JE (1998) Inorg Chim Acta
270:467
11. Johansson L, Ryan OB, Tilset M (1999) J Am Chem Soc 121:1974
12. Wick DD, Goldberg KI (1997) J Am Chem Soc 119:10235
13. Periana RA, Taube DJ, Gamble S, Taube H, Satoh T, Fujii H (1998) Science 280:560
14. Johnson JA, Li N, Sames D (2002) J Am Chem Soc 124:6900
15. Dangel BD, Godula K, Youn SW, Sezen B, Sames D (2002) J Am Chem Soc 124:11856
16. Ryabov AD (1985) Synthesis 233
17. Baldwin JE, Jones RH, Najera C, Yus M (1985) Tetrahedron 41:699
18. Balavoine G, Clinet JC (1990) J Organomet Chem 390:C84
19. Dyker G (1997) Chem Ber/Recl 130:1567
20. Zaitsev VG, Shabashov D, Daugulis O (2005) J Am Chem Soc 127:13154
21. Daugulis O, Roane J, Tran LD (2015) Acc Chem Res 48(4):1053–1064
22. Rouquet G, Chatani N (2013) Angew Chem Int Ed Engl 52:11726
23. Reddy BVS, Reddy LR, Corey EJ (2006) Org Lett 8:3391
24. Feng Y, Chen G (2010) Angew Chem Int Ed 49:958
25. Walsh CT (2004) Science 303:1805
26. Sieber SA, Marahiel MA (2003) J Bacteriol 185:7036
27. Flynn DL, Zelle RE, Grieco PA (1983) J Org Chem 48:2424
28. Evans DA, Britton TC, Ellman JA (1987) Tetrahedron Lett 28:6141
29. Gutekunst WR, Baran PS (2011) J Am Chem Soc 133:19076
30. Filho RB, De Souza MP, Mattos MEO (1981) Phytochemistry 20:345
31. Lewis FD, Quillen SL, Hale PD, Oxman JD (1988) J Am Chem Soc 110:1261
32. Shabashov D, Daugulis O (2010) J Am Chem Soc 132:3965
33. Lafrance M, Gorelsky SI, Fagnou K (2007) J Am Chem Soc 129:14570
34. Gutekunst WR, Gianatassio R, Baran PS (2012) Angew Chem Int Ed 51:7507
35. Gutekunst WR, Baran PS (2014) J Org Chem 79:2430
36. Ting CP, Maimone TJ (2014) Angew Chem Int Ed 53:3115
37. Wasa M, Yu J-Q (2008) J Am Chem Soc 130:14058
38. He G, Zhao Y, Zhang S, Lu C, Chen G (2012) J Am Chem Soc 134:3
39. Nadres ET, Daugulis O (2012) J Am Chem Soc 134:7
40. Ye X, He Z, Ahmed T, Weise K, Akhmedov NG, Petersen JL, Shi X (2013) Chem Sci 4:3712
41. Zhang Q, Chen K, Rao W, Zhang Y, Chen F-J, Shi B-F (2013) Angew Chem Int Ed 52:13588
42. Sun W-W, Cao P, Mei R-Q, Li Y, Ma Y-L, Wu B (2014) Org Lett 16:480
43. Zhang S-Y, He G, Nack WA, Zhao Y, Li Q, Chen G (2013) J Am Chem Soc 135:2124
Applications of Catalytic Organometallic C(sp
3
)–H Bond Functionalization
151
Potier pour le De ´veloppement de la Chimie des Substances Naturelles et ses Applications for
financial support.
References
1. Dick AR, Sanford MS (2006) Tetrahedron 62:2439
2. Jazzar R, Hitce J, Renaudat A, Sofack-Kreutzer J, Baudoin O (2010) Chem Eur J 16:2654
3. Baudoin O (2011) Chem Soc Rev 40:4902
4. Li H, Li BJ, Shi ZJ (2011) Catal Sci Technol 1:191
5. Dastbaravardeh N, Christakakou M, Haider M, Schnu ¨rch M (2014) Synthesis 46:1421
6. McMurray L, O’Hara F, Gaunt MJ (2011) Chem Soc Rev 40:1885
7. Gutekunst WR, Baran PS (2011) Chem Soc Rev 40:1976
8. Yamaguchi J, Yamaguchi AD, Itami K (2012) Angew Chem Int Ed 51:8960
9. Johnson JA, Sames D (2000) J Am Chem Soc 122:6321
10. Holtcamp MW, Henling LM, Day MW, Labinger JA, Bercaw JE (1998) Inorg Chim Acta
270:467
11. Johansson L, Ryan OB, Tilset M (1999) J Am Chem Soc 121:1974
12. Wick DD, Goldberg KI (1997) J Am Chem Soc 119:10235
13. Periana RA, Taube DJ, Gamble S, Taube H, Satoh T, Fujii H (1998) Science 280:560
14. Johnson JA, Li N, Sames D (2002) J Am Chem Soc 124:6900
15. Dangel BD, Godula K, Youn SW, Sezen B, Sames D (2002) J Am Chem Soc 124:11856
16. Ryabov AD (1985) Synthesis 233
17. Baldwin JE, Jones RH, Najera C, Yus M (1985) Tetrahedron 41:699
18. Balavoine G, Clinet JC (1990) J Organomet Chem 390:C84
19. Dyker G (1997) Chem Ber/Recl 130:1567
20. Zaitsev VG, Shabashov D, Daugulis O (2005) J Am Chem Soc 127:13154
21. Daugulis O, Roane J, Tran LD (2015) Acc Chem Res 48(4):1053–1064
22. Rouquet G, Chatani N (2013) Angew Chem Int Ed Engl 52:11726
23. Reddy BVS, Reddy LR, Corey EJ (2006) Org Lett 8:3391
24. Feng Y, Chen G (2010) Angew Chem Int Ed 49:958
25. Walsh CT (2004) Science 303:1805
26. Sieber SA, Marahiel MA (2003) J Bacteriol 185:7036
27. Flynn DL, Zelle RE, Grieco PA (1983) J Org Chem 48:2424
28. Evans DA, Britton TC, Ellman JA (1987) Tetrahedron Lett 28:6141
29. Gutekunst WR, Baran PS (2011) J Am Chem Soc 133:19076
30. Filho RB, De Souza MP, Mattos MEO (1981) Phytochemistry 20:345
31. Lewis FD, Quillen SL, Hale PD, Oxman JD (1988) J Am Chem Soc 110:1261
32. Shabashov D, Daugulis O (2010) J Am Chem Soc 132:3965
33. Lafrance M, Gorelsky SI, Fagnou K (2007) J Am Chem Soc 129:14570
34. Gutekunst WR, Gianatassio R, Baran PS (2012) Angew Chem Int Ed 51:7507
35. Gutekunst WR, Baran PS (2014) J Org Chem 79:2430
36. Ting CP, Maimone TJ (2014) Angew Chem Int Ed 53:3115
37. Wasa M, Yu J-Q (2008) J Am Chem Soc 130:14058
38. He G, Zhao Y, Zhang S, Lu C, Chen G (2012) J Am Chem Soc 134:3
39. Nadres ET, Daugulis O (2012) J Am Chem Soc 134:7
40. Ye X, He Z, Ahmed T, Weise K, Akhmedov NG, Petersen JL, Shi X (2013) Chem Sci 4:3712
41. Zhang Q, Chen K, Rao W, Zhang Y, Chen F-J, Shi B-F (2013) Angew Chem Int Ed 52:13588
42. Sun W-W, Cao P, Mei R-Q, Li Y, Ma Y-L, Wu B (2014) Org Lett 16:480
43. Zhang S-Y, He G, Nack WA, Zhao Y, Li Q, Chen G (2013) J Am Chem Soc 135:2124
Applications of Catalytic Organometallic C(sp
3
)–H Bond Functionalization
151