The asymmetric conjugate addition of carbon and heteroatom nucleophiles to nitroalkenes
is a very interesting tool for the construction of highly functionalized synthetic building …

An organocatalyzed asymmetric Michael addition reaction has been established as the most
relevant and dynamic research area for the construction of chiral carbon‐carbon and carbon …

Spiro-epoxy/aziridine oxindole frameworks are considered as an efficient structural toolbox
to obtain C3-functionalised oxindole derivatives. These 3, 3′-spiro-cyclic precursors are …

The unprecedented efficiency, reliability and adaptability in drug discovery, with the growing
number of applications and impact, have made Click Chemistry fascinating to the scientific …

The formation of CC and CX bonds is a fundamental process in synthesis. In recent years
organocatalysis has become a powerful tool to achieve these steps in a highly …

The properties of high stability, inherent porosity, and tunable nature of porous organic
polymers (POPs) make these materials ideal catalytic nanoreactors, which can be …

An improved diaminomethylenemalononitrile organocatalyst, bearing a N, N‐disubstituted
structure, promoted enantioselective conjugate addition reaction of α‐branched aldehydes …

The catalytic enantioselective Michael reaction is the conjugate addition of a resonance‐
stabilized carbanion to an electron‐poor olefin (an αβ‐unsaturated carbonyl compound or a …

The application of six novel α, β-dipeptides as chiral organocatalysts in the asymmetric
Michael addition reaction between enolizable aldehydes and N-arylmaleimides or …

The application of amino acids and small peptides as asymmetric organocatalysts in the
aldol and conjugate addition reactions is a significant breakthrough in the past decade. The …