The chiral oxazoline motif is present in many ligands that have been extensively applied in a
series of important metal-catalyzed enantioselective reactions. This Review aims to provide …

Asymmetric A3 coupling has emerged as an important class of reactions to synthesise chiral
propargylamines. In this tutorial review, an up to date progress of this reaction, with …

Three-component dehydrogenative coupling reactions represent important and practical
methodologies for forging new C–N bonds and C–C bonds. Achieving highly all-in-one …

A mild visible‐light‐induced Pd‐catalyzed intramolecular C− H arylation of amides is
reported. The method operates by cleavage of a C (sp2)− O bond, leading to hybrid aryl Pd …

In recent years, the transition‐metal catalyzed three‐component coupling of an aldehyde, an
alkyne and an amine, commonly called A3 coupling has become a powerful tool in organic …

N, O-aminals, molecules bearing a geminally N, O-substituted (stereogenic) carbon center,
have been recently recognized as an important class of building blocks in organic synthesis …

Chiral propargyl amides are particularly useful structural units in organic synthesis. The
enantioselective synthesis of propargyl amide is highly desirable. Conventional approach …

The multicomponent reaction of aldehydes, amines, and alkynes, known as A3 coupling,
yields propargylamines, a valuable organic scaffold, and has received significant interest …

Isoindolinone structure is an important privileged scaffold found in a large variety of naturally
occurring as well as synthetic, biologically and pharmaceutically active compounds. Owing …

Electrosynthesis is recognized as one of the most powerful and sustainable methods in
organic chemistry. Recently, electrochemically enabled annulations of carbon‐carbon triple …