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Beyond Directing Groups: Transition‐Metal‐Catalyzed CH Activation of Simple Arenes
Author(s) -
Kuhl Nadine,
Hopkinson Matthew N.,
WencelDelord Joanna,
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.201203269
Subject(s) - reactivity (psychology) , regioselectivity , surface modification , selectivity , catalysis , chemistry , benzene , combinatorial chemistry , transition metal , chelation , organic chemistry , medicine , alternative medicine , pathology
The use of coordinating moieties as directing groups for the functionalization of aromatic CH bonds has become an established tool to enhance reactivity and induce regioselectivity. Nevertheless, with regard to the synthetic applicability of CH activation, there is a growing interest in transformations in which the directing group can be fully abandoned, thus allowing the direct functionalization of simple benzene derivatives. However, this approach requires the disclosure of new strategies to achieve reactivity and to control selectivity. In this review, recent advances in the emerging field of non‐chelate‐assisted CH activation are discussed, highlighting some of the most intriguing and inspiring examples of induction of reactivity and selectivity.
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