Nitrones are important compounds and are highly useful in many aspects. The first part
describes the methods for synthesis of nitrones, which are useful and environmentally …

Bioorthogonal chemical reactions have emerged as convenient and rapid methods for
incorporating unnatural functionality into living systems. Different prototype reactions have …

Abstract The regio‐and enantioselective (3+ 3) cycloaddition of nitrones with 2‐
indolylmethanols was accomplished by the cooperative catalysis of hexafluoroisopropanol …

A green and sustainable synthetic strategy for amide bond formation utilizing a visible light-
promoted nitrone formation/rearrangement cascade was developed. This method utilized …

By resorting to the principle of remote activation, we herein demonstrate the first photoredox
catalyzed (3+ 3) dipolar cycloaddition of nitrones with aryl cyclopropanes. Key to the fidelity …

Functionalizable directing groups (DGs) are highly desirable in C− H activation chemistry.
The nitrone DGs are explored in rhodium (III)‐catalyzed C− H activation of arenes and …

Azetidines are four-membered nitrogen-containing heterocycles that hold great promise in
current medicinal chemistry due to their desirable pharmacokinetic effects. However, a lack …

Chiral amino acids (AAs), being the main “building” blocks of the living organisms, are also
an important class of organic compounds which broadly applied in synthetic chemistry …

The enantio‐and chemoselective iridium‐catalyzed N‐allylation of oximes is described for
the first time. Intramolecular kinetic resolution provides access to cyclic nitrones and …

We report realization of the first enantioselective Cope-type hydroamination of oximes for
asymmetric nitrone synthesis. The ligand promoted asymmetric cyclopropene …