The smallest strained, saturated N-heterocycles, such as aziridine, can be a valuable
building block in synthetic organic chemistry. Ring-opening reactions with various …

Tetrahydroquinoxalines are found in many biologically and pharmacologically active small
molecules. In the past two decades, significant progress has been made in the development …

TiO 2-SiO 2 composites with different Ti/Si atomic ratios were synthesized by an optimized
pre-hydrolysis-co-precipitation method while the corresponding NiMo supported …

A simple one-pot, two-step strategy for the synthesis of tetrahydro-1 H-azepino [4, 3, 2-cd]
indoles via Lewis acid-catalyzed SN2-type ring opening of activated azetidines with 4 …

A metal-free, conjugated organic polymer (TPA-PQ)-catalyzed intramolecular C–H
functionalization strategy for the synthesis of imidazolidines in the presence of light and O2 …

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 …

This report illustrates BF3· OEt2 promoted intramolecular cascade cycloaromatization of 1, 7-
ynones toward synthesizing structurally diverse benzofluorene scaffolds. Remarkably, the …

Abstract Imidazo [1, 2-a] pyridines are present in numerous biologically active compounds
as the core structural motif. Herein, we report an asymmetric interrupted Barton-Zard …

Heterocyclic compounds are of main interest in medicinal chemistry. The most complex
branches of chemistry are normally heterocyclic chemistry. Most synthetic heterocyclic …

A metal-free photoinduced triiodide-mediated [3+ 2] cycloaddition of N-Ts aziridines with
alkenes is described herein. This operationally simple protocol utilized bench-stable and …