VO(acac)(2)-CeCl(3) combo catalyst has been developed for chemoselective cyclocondensation cum oxidation under mild reaction conditions toward synthesis of a new class of optically pure compounds, 2-(2'-C-3',4',6'-tri-O-benzyl/methyl-glycal)-1H-benzimidazoles. It involves an operationally simple synthetic protocol efficient for the syntheses of a wide range of chiral benzimidazoles in high yields without formation of undesired 1,2-disubstituted and pseudoglycal byproducts. Vanadium(V) is found as active oxidant for the chemical processes which is investigated by UV absorption spectroscopy. Highly ordered one-dimensional low molecular mass organic nanostructured materials are fabricated by nanocrystallization of the chiral nanoscale building blocks. Theoretical calculation by the B3LYP/6-31G** level of theory of the glycal-based chiral benzimidazoles shows out of planar geometry of the 1H-anthra[1,2-d]imidazole-6,11-dione moiety, which is responsible for the strong self-aggregation to generate ultralong nanostructured materials. We have also found nice agreement between the theoretical results with the experimental observation in 2D-NOESY experiments. The photophysical property of the solid nanostructured materials is also reported.

A highly efficient strategy for chemoselective oxidation of aldoximes to nitrile oxides by iodosobenzene in neutral aqueous media is reported. Their in situ intermolecular 1,3-dipolar cycloaddition (1,3-DC) with olefins in nanometer aqueous micelles occurs with improved stereoselectivity and acceleration of reaction rate toward synthesis of new chiral synthons, 3-(2'-C-3',4',6'-tri-O-benzylglycal)-Delta(2)-isoxazolines and others. Construction of optically pure 2,8-dioxabicyclo[4.4.0]decene skeleta is performed by this green approach, and the stereochemistry of the new chiral center is predicted by B3LYP density functional theory.

Lawesson's reagent is a classic example of a compound having a remarkable construction and also a distinctive chemical behaviour that can challenge stereotype conceptual explanations. At the very beginning, it was mainly known for its use in the thionation of various types of carbonyl groups. However, over the last few years chemists reported some appealing examples which can nurture the chemistry community to perceive innovative ideas. These include the construction of valuable heterocycles, important coupling reactions, and the decoration of metal‐based attractive cores. Several important reports provided comprehensive theoretical studies regarding mechanistic classification. This article gives an overview of the recent insights and synthetic applications of this famous reagent from 2013 to 2019.

Activation of π-bond with organic Lewis acid and cationic surfactant mediated direct transfer of halides to alkyne and alkene are demonstrated to afford α,α-dihaloketones and other valuable synthons with outstanding selectivities.

The powerful cyclization and tandem oxidation property of environmentally benign PhIO is developed for the first time, which leads to regiospecific [3+2]-tandem oxidative cyclization of imine at room temperature in rapid access to a new class of compounds, 1,2-functionalized 4,5-diarylimidazoles, in excellent yield with synthetic efficiency. Size, shape, and activity of the involved nanoreactors for the green approach built up from various surfactants are investigated. Spontaneous generation of low molecular mass self-aggregated organic materials, their cofacial one-dimensional packing, and interesting photophysical properties are reported.

Generation of azomethine imine and its scope in regioselective 1,3-dipolar cycloaddition (DC) of imine with PhIO toward highly substituted Delta(2)-1,2,4-triazoline, 1,2,4-triazole, and their fused, chiral, and sugar-based analogues are demonstrated.

Intramolecular formal 1,3-dipolar cycloaddition of ketoimine is developed with PhIO for the first synthesis of fused-Δ(1)-pyrrolines. The scope of the reaction, complete diastereoselectivity and its rationalization by a computational study are reported.

Molecules bearing three primary amine groups are ubiquitous substances in various fields of synthetic chemistry. Some of them are commercially available and the rests are emerged from the designed protocols of synthetic chemists. It has been observed that such aliphatic as well as aromatic triamines are excellent precursors for the design and synthesis of various cage molecules of which organic imine cages (OICs) and related amine macrocycles belong to the category of special interest. These compounds possess unique architectures and already made their marks in the field of supramolecular chemistry, synthetic methodology, and material science. In this review we aimed to consider recent reports that highlighted the syntheses, special features, and applications of primary triamine based OICs and related amine macrocycles.