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- W2951796212 abstract "Stoichiometric cycloruthenation reactions of substrates containing Lewis-basic functionalities set the stage for efficient ruthenium-catalyzed C–H bond 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 economically and environmentally benign alternatives to traditional cross-coupling chemistry." @default.
- W2951796212 created "2019-06-27" @default.
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- W2951796212 date "2011-06-03" @default.
- W2951796212 modified "2023-09-26" @default.
- W2951796212 title "ChemInform Abstract: Ruthenium-Catalyzed Direct Arylations Through C-H Bond Cleavages" @default.
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- W2951796212 doi "https://doi.org/10.1002/chin.201126245" @default.
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