Titlebook: C-H Activation; Jin-Quan Yu,Zhangjie Shi Book 2010 Springer-Verlag Berlin Heidelberg 2010 Azine.Azole.C-H Activation.C-H Functionalization

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The Kiel Bight as Research Area,d functionalization reactions. Thereby, selective addition reactions of C–H bonds across alkenes or alkynes enabled atom-economical synthesis of substituted arenes. More recently, ruthenium-catalyzed direct arylation reactions were examined, which display an unparalleled scope and, hence, represent

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https://doi.org/10.1007/978-3-030-36192-1ion and the potential to streamline synthesis by the elimination of pre-activation of coupling reagents. In this chapter, recent developments in oxidative cross-coupling reactions will be presented with the focus on the functionalization of sp3 C–H bonds with other C–H bonds

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,Cross-Dehydrogenative Coupling Reactions of sp3-Hybridized C–H Bonds,ion and the potential to streamline synthesis by the elimination of pre-activation of coupling reagents. In this chapter, recent developments in oxidative cross-coupling reactions will be presented with the focus on the functionalization of sp3 C–H bonds with other C–H bonds

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0340-1022 mistry, each written by the world renowned experts.Still valTable of Contents- Synthesis in the Key of Catellani: Norbornene-Mediated ortho C–H Functionalization - Mechanistic Considerations in the Development and Use of Azine, Diazine and Azole N-Oxides in Palladium-Catalyzed Direct Arylation- Pall

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