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[Rh III Cp*]‐Catalyzed Dehydrogenative ArylAryl Bond Formation
Author(s) -
WencelDelord Joanna,
Nimphius Corinna,
Patureau Frederic W.,
Glorius Frank
Publication year - 2012
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201107842
Subject(s) - aryl , catalysis , chemistry , medicinal chemistry , organic chemistry , alkyl
Directed, undirected! Rhodium(III)‐catalyzed double CH bond activation (one directed, one undirected) provides an efficient route to biaryls (see scheme; DG=directing group). Significant kinetic isotope effects for both reaction partners and H/D scrambling between them are interesting experimental findings. While the mechanism is still unclear, a rhodium(V) species is invoked in the catalytic cycle.
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