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Alkane C–H Oxygenation Catalyzed by Transition Metal Complexes

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Alkane C-H Activation by Single-Site Metal Catalysis

Part of the book series: Catalysis by Metal Complexes ((CMCO,volume 38))

Abstract

Alkane oxidation reactions are of fundamental importance in bulk and fine chemistry, but the inert character of alkyl C–H bonds poses formidable challenges to the design of reagents that could enable their selective oxidation. Highly reactive-oxidizing reagents are needed, and this factor poses major problems in terms of chemo and regioselectivity. Despite all these conditionings, because of its technological and biological significance and implications, and because of the fundamental scientific challenge that selective oxidation of sp3 C–H bonds represents, research in the field is rich, and major breakthroughs have appeared over the last years. Collected and discussed in the following pages are metal-based systems that mediate the catalytic oxidation of alkane C–H bonds leading to C–O bond formation under homogeneous conditions, and where organometallic interactions do not participate in the C–H bond breakage. The chapter has been focused in systems that have specific synthetic and or biological relevance, and/or cases where well-defined transition metal catalysts have been studied.

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Acknowledgments

Anna Company and Julio Lloret thank MICINN for Ramon Y Cajal Contracts. Financial support via ICREA-Academia Award to MC, Catalan SGR 2009-SGR637, MICINN-Spain (CTQ2009-08464/BQU), the European Research Foundation for Project ERC-2009-StG-239910 and Consolider Ingenio/CSD2010-00065.

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Company, A., Lloret, J., Gómez, L., Costas, M. (2012). Alkane C–H Oxygenation Catalyzed by Transition Metal Complexes. In: Pérez, P. (eds) Alkane C-H Activation by Single-Site Metal Catalysis. Catalysis by Metal Complexes, vol 38. Springer, Dordrecht. https://doi.org/10.1007/978-90-481-3698-8_5

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