4.8 Editorial Material

Atroposelective remote meta-C-H arylation of 2-arylanilines

Journal

CHEM
Volume 9, Issue 6, Pages 1347-1349

Publisher

CELL PRESS
DOI: 10.1016/j.chempr.2023.05.022

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Enantioselective remote C-H activation is a challenging task in organic chemistry, and atroposelective synthesis of remotely substituted axially chiral molecules via direct C-H activation remains elusive. In this issue of Chem, Yu, Wang, and co-workers report an atroposelective meta-C-H arylation of 2-arylanilines via an enantioselective palladation relay strategy.
Enantioselective remote C-H activation is a challenging task in organic chemistry, and atroposelective synthesis of remotely substituted axially chiral molecules via direct C-H activation remains elusive. In this issue of Chem, Yu, Wang, and co-workers report an atroposelective meta-C-H arylation of 2-arylanilines via an enantioselective palladation relay strategy.

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