The demand for practical methods for the synthesis of novel fluoroalkyl molecules is
increasing owing to their diverse applications. Our group has achieved efficient …

Due to the significance of organofluorine compounds in disciplines ranging from medicine to
agriculture to materials science, the invention of new methods for the creation of carbon …

The mild generation of nitrogen-centred radicals from N–F reagents has become a
convenient synthetic tool. This methodology provides access to the aminative …

N-Heterocycles constitute an important structural moiety of small molecules in
pharmaceuticals and agrochemicals. Fluorination of heterobenzylic C–H bonds in these …

Selective functionalization of a single sp3 C–F bond of the CF3 group represents an
appealing way to generate the pharmaceutically privileged difluoromethylene moiety …

A copper‐catalyzed cascade difunctionalization of unactivated olefins with readily available
Rf‐I reagents to construct Csp3− CF2/C− C bonds has been reported. This strategy provides …

Fluorine incorporation into organic molecules is expected to lower the pKa of neighboring
functionality via its strong electron‐withdrawing effect, and this strategy has been widely …

Trifluoromethyl ketones are important enzyme inhibitors and versatile synthons for the
preparation of trifluoromethylated heterocycles and complex molecules. An efficient …

Given the widespread applications of fluorinated substances in pharmaceuticals, biology,
and materials, the development of fluorine-containing building blocks remains an important …

The current Account gives an insight into the synthesis of some N-heterocyclic β-amino acid
derivatives and various functionalized saturated azaheterocycles accessed from substituted …