Ruthenium( ii )-catalyzed C–H functionalizations on benzoic acids with aryl, alkenyl and alkynyl halides by weak-O-coordination
2016 | journal article. A publication with affiliation to the University of Göttingen.
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Ruthenium( ii )-catalyzed C–H functionalizations on benzoic acids with aryl, alkenyl and alkynyl halides by weak-O-coordination
Mei, R.; Zhu, C. & Ackermann, L. (2016)
Chemical Communications, 52(89) pp. 13171-13174. DOI: https://doi.org/10.1039/C6CC07773K
Documents & Media
Details
- Authors
- Mei, Ruhuai; Zhu, Cuiju; Ackermann, Lutz
- Abstract
- C–H arylations of weakly coordinating benzoic acids were achieved by versatile ruthenium( ii ) catalysis with ample substrate scope.
C–H arylations of weakly coordinating benzoic acids were achieved by versatile ruthenium( ii ) catalysis with ample substrate scope. Thus, user-friendly ruthenium( ii ) biscarboxylate complexes modified with tricyclohexylphosphine enabled C–H functionalizations with aryl electrophiles. The unique versatility of the ruthenium( ii ) catalysis manifold was reflected by facilitating effective C–H activations with aryl, alkenyl and alkynyl halides. - Issue Date
- 2016
- Journal
- Chemical Communications
- ISSN
- 1359-7345
- eISSN
- 1364-548X
- ISSN
- 1359-7345
- eISSN
- 1364-548X
- Language
- English
