The development of NH transfer reactions using hypervalent iodine and simple sources of
ammonia has facilitated the synthesis of sulfoximines and sulfonimidamides for applications …

In recent years, there has been a notable surge in the prominence of enantioenriched sulfur
(VI) compounds within the chemical science, particularly in the realm of bioactive molecules …

The sulfinamidines as aza analogues of sulfinamides received limited attention from both
organic chemists and pharmaceutical chemists. Herein, we present a tandem …

In this study, we present a novel, efficient method for the oxidative amination of sulfenamides
using diacetoxyiodobenzene (PhI (OAc) 2) and amines under basic conditions. This …

Abstract Sulfur (VI)‐fluoride exchange (SuFEx) chemistry, an all‐encompassing term for
substitution events that replace fluoride at an electrophilic sulfur (VI), enables the rapid and …

A mechanochemical copper-catalyzed oxidative amination of primary sulfinamides has been
developed, leading to N H-sulfonimidamides in moderate to good yields under solvent-free …

A CuBr2-catalyzed cascade reaction of amidines with exocyclic α, β-unsaturated
cycloketones was developed, affording a large variety of spiroimidazolines in moderate to …

Sulfur monoxide (SO) is a highly reactive species that cannot be isolated in bulk. However,
SO can play a pivotal role as a fundamental building block in organic synthesis. Reported …

Sulfur-containing compounds are found in myriad applications. Sulfones and sulfonamides
are the most common functional groups used in medicinal and agrochemical endeavours …

Herein, we disclose a visible‐light‐induced rhodium‐catalyzed oxidative C− H/N− H bond
activation of sulfonimidamides (SIAs) and subsequent [4+ 2] annulation with an alkyne in …