Aziridines are the saturated three-membered cyclic amines that constitute an important
group of synthetic intermediates. These could act as a precursor for diverse organic …

The transition-metal-aided stereoselective construction of sp3-carbon-rich heterocyclic
scaffolds using strained-ring systems has received considerable attention in recent years …

Metal-free heterogeneous catalysis provides a promising strategy for the multicomponent
synthesis of valuable imidazolidines, which are ubiquitous structural moieties found in a …

A visible light-induced palladium-catalyzed oxidative C–H alkylation of oximes has been
developed. This mild protocol allows for an efficient atom economical C–C bond …

Chiral imidazolidine shows its potential in multiple fields. However, direct catalytic
asymmetric construction of chiral imidazolidines is still limited. Herein, we report an effective …

The first organocatalytic asymmetric [3+ 2]-annulation of γ-sulfonamido-α, β-unsaturated
ketones with cyclic N-sulfimines has been developed, and enantioenriched functionalized …

Chiral heterocyclic compounds are an important class of chiral substances, which are
widespread in many chiral drugs, pesticides and catalysts. Therefore, the efficient …

Piperidine scaffolds are present in a wide range of bioactive natural products and are
therefore considered as highly valuable, privileged synthetic targets. In this manuscript, we …

Activated aziridines react with propargyl alcohols in the presence of Zn (OTf) 2 as the Lewis
acid catalyst following an SN2-type ring-opening mechanism to furnish the corresponding …

Five membered N‐heterocycles are significant targets in organic synthesis because of their
ubiquitous existence in bioactive natural products and pharmaceuticals. Over the past …