Abstract α-Amino nitrile compounds have a profound impact on bio-chemical sciences, as
they have been prepared from inexpensive starting materials and have become valuable …

This review focuses on the utilization of indium (III) as π-acid for the activation of C–C
unsaturated bonds in organic synthesis. In addition to its well-known σ-coordination with …

With the aim of developing new highly porous, heterogeneous Lewis acid catalysts for
multicomponent reactions, a new mesoporous metal–organic framework, InPF-110 ([In3O …

This review describes the efforts in the synthesis of pyrrole derivatives using the reaction of
alkynes with nitrogen‐compounds under transition metal‐catalyzed and metal‐free …

A novel protocol for the synthesis of α-aryl nitriles has been successfully achieved via a
copper-catalyzed cyanation of N-tosylhydrazones employing thiocyanate as the source of …

The rational design and successful synthesis of novel functional metal–organic frameworks
relies on careful selection of metals and versatile organic ligands. A newly designed …

We disclose herein the first synthetic method that is capable of offering heteroaryl [b]
quinolines (HA [b] Qs) with structural diversity, which include tricyclic and tetracyclic …

Abstract An oxidative [3+ 3] annulation of atropaldehyde acetals with various 1, 3‐
bisnucleophiles was developed using either N‐bromosuccinimide or copper (II) bromide as …

Treatment of N-substituted pyrroles with carbonyl compounds and nucleophiles under
indium catalysis was found to be a promising method for preparing β-alkylpyrroles without …

The direct amination of cyanohydrins with amines via a catalytic cyano-borrowing reaction
was developed. The transformation features broad substrate scope, excellent functional …