10
8. Li CJ (2009) Cross-dehydrogenative coupling (CDC): exploring C-C bond formations beyond
functional group transformations. Acc Chem Res 42:335–344. https://doi.org/10.1021/
ar800164n
9. Liu C, Jin L, Lei A (2010) Transition-metal-catalyzed oxidative cross-coupling reactions.
Synlett 2010:2527–2536. https://doi.org/10.1055/s-0030-1258802
10. Liu C, Zhang H, Shi W, Lei A (2011) Bond formations between two nucleophiles: transition
metal catalyzed oxidative cross-coupling reactions. Chem Rev 111:1780–1824. https://doi.
org/10.1021/cr100379j
11. Liu C, Liu D, Lei A (2014) Recent advances of transition-metal catalyzed radical oxidative
cross-couplings. Acc Chem Res 47:3459–3470. https://doi.org/10.1021/ar5002044
12. Liu C, Yuan J, Gao M, Tang S, Li W, Shi R, Lei A (2015) Oxidative coupling between two
hydrocarbons: an update of recent C-H Functionalizations. Chem Rev 115:12138–12204.
https://doi.org/10.1021/cr500431s
13. Meijere AD, Diederich F (2004) Metal-catalyzed cross-coupling reactions. 2nd, completely
rev. and enl. Edn. Wiley-VCH, Weinheim
14. Milstein D, Stille JK (1979) Palladium-catalyzed coupling of tetraorganotin compounds with
aryl and benzyl halides. Synthetic utility and mechanism. J Am Chem Soc 101:4992–4998.
https://doi.org/10.1021/ja00511a032
15. Miyaura N, Suzuki A (1979) Stereoselective synthesis of arylated (E)-alkenes by the reaction
of alk-1-enylboranes with aryl halides in the presence of palladium catalyst. J Chem Soc Chem
Commun:866. https://doi.org/10.1039/c39790000866
16. Reniers GLL, Brebbia CA (2011) Sustainable chemistry. WIT transactions on ecology and the
environment, vol 154. WIT Press, Southampton/Boston
17. Shi W, Liu C, Lei A (2011) Transition-metal catalyzed oxidative cross-coupling reactions to
form C-C bonds involving organometallic reagents as nucleophiles. Chem Soc Rev 40:2761–
2776. https://doi.org/10.1039/C0CS00125B
18. Stuart DR, Fagnou K (2007) The catalytic cross-coupling of unactivated arenes. Science
316:1172–1175. https://doi.org/10.1126/science.1141956
19. Wan X, Ma Z, Li B, Zhang K, Cao S, Zhang S, Shi Z (2006) Highly selective C-H functionalization/halogenation of acetanilide. J Am Chem Soc 128:7416–7417. https://doi.org/10.1021/
ja060232j
20. Wang P, Zhao G, Wang Y, Lu Y (2017) MnTiO3-driven low-temperature oxidative coupling of
methane over TiO2-doped Mn2O3-Na2WO4/SiO2 catalyst. Sci Adv 3:e1603180. https://doi.
org/10.1126/sciadv.1603180
21. Zhao Y, Wang H, Hou X, Hu Y, Lei A, Zhang H, Zhu L (2006) Oxidative cross-coupling
through double transmetallation: surprisingly high selectivity for palladium-catalyzed crosscoupling of alkylzinc and alkynylstannanes. J Am Chem Soc 128:15048–15049. https://doi.
org/10.1021/ja0647351
C. Liu
8. Li CJ (2009) Cross-dehydrogenative coupling (CDC): exploring C-C bond formations beyond
functional group transformations. Acc Chem Res 42:335–344. https://doi.org/10.1021/
ar800164n
9. Liu C, Jin L, Lei A (2010) Transition-metal-catalyzed oxidative cross-coupling reactions.
Synlett 2010:2527–2536. https://doi.org/10.1055/s-0030-1258802
10. Liu C, Zhang H, Shi W, Lei A (2011) Bond formations between two nucleophiles: transition
metal catalyzed oxidative cross-coupling reactions. Chem Rev 111:1780–1824. https://doi.
org/10.1021/cr100379j
11. Liu C, Liu D, Lei A (2014) Recent advances of transition-metal catalyzed radical oxidative
cross-couplings. Acc Chem Res 47:3459–3470. https://doi.org/10.1021/ar5002044
12. Liu C, Yuan J, Gao M, Tang S, Li W, Shi R, Lei A (2015) Oxidative coupling between two
hydrocarbons: an update of recent C-H Functionalizations. Chem Rev 115:12138–12204.
https://doi.org/10.1021/cr500431s
13. Meijere AD, Diederich F (2004) Metal-catalyzed cross-coupling reactions. 2nd, completely
rev. and enl. Edn. Wiley-VCH, Weinheim
14. Milstein D, Stille JK (1979) Palladium-catalyzed coupling of tetraorganotin compounds with
aryl and benzyl halides. Synthetic utility and mechanism. J Am Chem Soc 101:4992–4998.
https://doi.org/10.1021/ja00511a032
15. Miyaura N, Suzuki A (1979) Stereoselective synthesis of arylated (E)-alkenes by the reaction
of alk-1-enylboranes with aryl halides in the presence of palladium catalyst. J Chem Soc Chem
Commun:866. https://doi.org/10.1039/c39790000866
16. Reniers GLL, Brebbia CA (2011) Sustainable chemistry. WIT transactions on ecology and the
environment, vol 154. WIT Press, Southampton/Boston
17. Shi W, Liu C, Lei A (2011) Transition-metal catalyzed oxidative cross-coupling reactions to
form C-C bonds involving organometallic reagents as nucleophiles. Chem Soc Rev 40:2761–
2776. https://doi.org/10.1039/C0CS00125B
18. Stuart DR, Fagnou K (2007) The catalytic cross-coupling of unactivated arenes. Science
316:1172–1175. https://doi.org/10.1126/science.1141956
19. Wan X, Ma Z, Li B, Zhang K, Cao S, Zhang S, Shi Z (2006) Highly selective C-H functionalization/halogenation of acetanilide. J Am Chem Soc 128:7416–7417. https://doi.org/10.1021/
ja060232j
20. Wang P, Zhao G, Wang Y, Lu Y (2017) MnTiO3-driven low-temperature oxidative coupling of
methane over TiO2-doped Mn2O3-Na2WO4/SiO2 catalyst. Sci Adv 3:e1603180. https://doi.
org/10.1126/sciadv.1603180
21. Zhao Y, Wang H, Hou X, Hu Y, Lei A, Zhang H, Zhu L (2006) Oxidative cross-coupling
through double transmetallation: surprisingly high selectivity for palladium-catalyzed crosscoupling of alkylzinc and alkynylstannanes. J Am Chem Soc 128:15048–15049. https://doi.
org/10.1021/ja0647351
C. Liu