Ruthenium-Catalyzed Regioselective C–H Alkenylation Directed by a Free Amino Group
2013
Suzuki, Chiharu | Hirano, Koji | Satoh, Tetsuya | Miura, Masahiro
The ruthenium-catalyzed alkenylation reactions of 2-aminobiphenyls and cumylamine proceed smoothly to produce the corresponding regioselectively alkenylated products. These reactions involve a C–H bond cleavage directed by their free amino groups.
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Bibliographic information
Publisher
American Chemical Society
Other Subjects
Chemical bonding; Cleavage (chemistry); Regioselectivity
Language
English
Type
Journal Article; Text
2024-02-28
MODS
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