Due to their inherent ring strain, three-membered carbocyclic-and heterocyclic ring
structures are versatile synthetic building blocks. Traditional ring-opening methods of these …

Carbon− heteroatom bond formations are very important reactions in organic synthesis and
have attracted the interest of many synthetic organic chemists, leading them to develop new …

Aziridines—three-membered nitrogen-containing cyclic molecules—are important synthetic
targets. Their substantial ring strain and resultant proclivity towards ring-opening reactions …

An unprecedented Pd‐catalyzed fluorinative bifunctionalization of aziridines and azetidines
was successfully developed via regioselective C− C and C− F bond cleavage of gem …

In general, the P-centered ring-opening of quaternary phosphirenium salts (QPrS)
predominantly leads to hydrophosphorylated products, while the C-centered ring-opening is …

The utilization of easily recyclable biosorbent material with ultrahigh adsorption capacity for
the removal of heavy metal ions from aqueous environments is an important step towards …

A Ni-catalyzed reductive cross-coupling of styrenyl aziridines with aryl iodides is reported.
This reaction proceeds by a stereoconvergent mechanism and is thus amenable to …

An efficient method for the reductive cross-electrophile coupling of aziridines with aryl
halides using nickel electrocatalysis is reported. This reaction provides valuable …

The past decade has witnessed the golden age of homogeneous gold-catalyzed reactions,
especially those that involve the transformation of highly strained molecules into complex …

Among the variously functionalized aziridines, 1 vinylaziridines and ethynylaziridines are
increasingly being exploited as versatile building blocks in organic synthesis. Compounds of …