Related Experiment Video
Updated: Feb 6, 2026

Quantification of the Respiratory Burst Response as an Indicator of Innate Immune Health in Zebrafish
Published on: September 12, 2013
Beyond Friedel and Crafts: Innate Alkylation of C-H Bonds in Arenes
Gwilherm Evano1, Cédric Theunissen1
1Laboratoire de Chimie Organique, Service de Chimie et Physico-Chimie Organiques, Université libre de Bruxelles (ULB), Avenue F.D. Roosevelt 50, CP160/06, 1050, Brussels, Belgium.
Abstract:
Alkylated arenes are ubiquitous molecules and building blocks commonly utilized in most areas of science. Despite its apparent simplicity, the regioselective alkylation of arenes is still a challenging transformation in a lot of cases. Classical methods for the introduction of alkyl groups to arenes, such as the venerable Friedel-Crafts reaction, radical additions, metalation or prefunctionalization of the arene followed by further alkylation, as well as alternatives such as the directed alkylation of C-H bonds, still suffer from severe limitations in terms of scope, efficiency, and selectivity. This can be addressed by exploiting the innate reactivity of some (hetero)arenes, in which electronic and steric properties, governed (or not) by the presence of one (or multiple) heteroatom(s), ensure high levels of regioselectivity. These innate alkylations of C-H bonds in (hetero)arenes will be overviewed comprehensively in this Review.
Related Concept Videos
Electrophilic Aromatic Substitution: Friedel–Crafts Alkylation of Benzene
Limitations of Friedel–Crafts Reactions
Electrophilic Aromatic Substitution: Friedel–Crafts Acylation of Benzene
Bond Energies and Bond Lengths
Peptide Bonds
Bonding in Metals

