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47. , and Plastina, P. (2008) J. Org. , 73, 756–759. J. (1996) Chem. , 2115–2116. C. , 41, 3891–3893. C. (1998) Synth. , 28, 849–857. Y. (2010) J. Organomet. , 695, 1744–1748. (a) Dhawan, R. A. (2004) J. Am. Chem. , 126, 468–469. (b) Lu, Y. A. (2008) Angew. Chem. Int. , 47, 5430–5433. R. A. (2006) J. Am. Chem. , 128, 6050–6051. A. (2011) J. Org. , 76, 170–180. A. (2011) Angew. Chem. Int. , 50, 8948–8951. A. (2003) J. Am. Chem. , 125, 1474–1475. , and Alper, H. (2008) Org. , 10, 4899–4901. C. (2009) Org.

Transition-metal catalysts play an ever-increasing and important role in modern chemistry [3]. Numerous transition-metal-catalyzed coupling reactions have been developed and applied in the total synthesis of natural products, such as the Suzuki reaction, the Negishi reaction, the Heck reaction, and many others [4]. Interestingly, the power of transition-metal catalysts is even more visible in the area of domino reactions, where terms such as palladium walking show the value of transition metals in bond formations.

97–121. 5. (a) Pellissier, H. (2013) Chem. , and Garcia-Tellado, F. (2013) Chem. Soc. , and Langer, P. , and Poli, G. (2012) in Innovative Catalysis in Organic Synthesis (ed. G. Andersson), Wiley-VCH Verlag GmbH, Weinheim, pp. 47–76; (e) Galestokova, Z. and Sebesta, R. (2012) Eur. J. Org. -M. (2012) Angew. Chem. Int. K. J. C. R. , 14, 1821–1849; (j) Grossmann, A. and Enders, D. (2012) Angew. Chem. Int. , 51, 314–325; (k) Perumal, S. C. (2011) in Targets in Heterocyclic Systems, Vol. A. Attanasi and D.

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An introduction to surface chemistry by Eric Keightley Rideal.


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