The construction of carbon‐fluorine bonds is an important yet challenging task in organic
synthesis. Transition metal‐catalyzed/‐mediated C− F bond forming processes have …

A general method for synthesizing optically active, primary, secondary, and tertiary
organofluorides was developed. This chiral pool synthesis utilized the skeleton of arabinose …

Indolin-3-ones are essential heterocycles with wide-ranging biological activities and
medicinal values, and therefore, efficient approaches to their synthesis remain in demand …

The diverse structures of DNA serve as potent chiral scaffolds for DNA-based asymmetric
catalysis, yet in most cases tens to hundreds of nucleotides in DNA hybrid catalysts hinder …

The field of enantioselective CX bond formation (X= halogen, S, Se) has grown steadily over
the past decade. It is particularly true of electrophilic enantioselective fluorination owing to …

Enantioselective CN, CC, CF and CS functionalization of 2-substituted-indolin-3-ones has
been developed for the synthesis of chiral 3-oxoindoline-2-carboxylate scaffolds using chiral …