Enantioselective C–H activation is one of the promising methods to obtain enantiopure
molecules in high enantiomeric excess with excellent control of regio and chemo-selectivity …

Transition-metal-catalyzed directed C–H alkenylation with maleimides has attracted much
attention in recent years, as maleimide core moieties are present in various natural products …

Herein, atroposelective synthesis of axially chiral biaryls with unactivated olefins by a
palladium-catalyzed C–H olefination using a chiral transient directing group strategy has …

The atroposelective direct C–H alkylation of heterobiaryls with simple alkenes represents a
challenging and underexplored frontier. Herein we report an iridium (I)-catalyzed …

In order to directly functionalize C− H bonds of complex molecules and, in particular, to
control the regioselectivity of the reaction, a wide range of directing groups has been used …

A comparative study of C8-alkylation of isoquinolone with maleimides is reported under
different catalytical systems. Among different catalytical systems, Ru and Rh catalysts were …

An efficient Rh (III)‐catalyzed C− H alkenylation of N‐protected isoquinolone with
maleimides is reported. The carbonyl group of isoquinolone acts as an inherent directing …

Metal-catalyzed allenylic substitution reactions where allenes serve as electrophilic
precursors have been recognized as a rapid way for novel allene construction. On the …

Herein, a concise protocol for the construction of axially chiral biaryls via Pd-catalysed direct
C–H arylation of 1-arylisoquinoline N-oxides through kinetic resolution using a commercially …

A strategy for Co (III)-catalyzed C (sp2)–H alkenylation of N-protected isoquinolones with 1,
4-naphthoquinones has been disclosed. The developed protocol was efficiently applied for …