Transition metal catalyzed manipulation of non-polar carbon-hydrogen bonds for synthetic purpose

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Abstract

The direct addition of ortho C-H bonds in various aromatic compounds such as ketones, esters, imines, imidates, nitriles, and aldehydes to olefins and acetylenes can be achieved with the aid of transition metal catalysts. The ruthenium catalyzed reaction is usually highly efficient and useful as a general synthetic method. The coordination to the metal center by a heteroatom in a directing group such as carbonyl and imino groups in aromatic compounds is the key step in this process. Mechanistically, the reductive elimination to form a C-C bond is the ratedetermining step, while the C-H bond cleavage step is not. © 2011 The Japan Academy.

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APA

Murai, S. (2011). Transition metal catalyzed manipulation of non-polar carbon-hydrogen bonds for synthetic purpose. Proceedings of the Japan Academy Series B: Physical and Biological Sciences. https://doi.org/10.2183/pjab.87.230

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