The development of the first intermolecular Rh2 (II)-catalyzed aziridination of olefins using
anilines as nonactivated N atom precursors and an iodine (III) reagent as the stoichiometric …

Abstract The [Rh2 (OAc) 4]‐catalyzed decomposition of NsN (DOUBLE BOND) IPh {[N‐(p‐
nitrobenzenesulfonyl) imino] phenyliodinane} in the presence of olefins affords aziridines in …

The [Rh2 (OAc) 4] catalyzed decomposition of (N-(p-nitrobenzenesulfonyl) imino)
phenyliodinane (PhI NNs) in the presence of olefins affords aziridines in yields of 18–85 …

A RhII‐catalyzed direct and stereospecific N‐H‐and N‐alkyl aziridination of olefins is
reported that uses hydroxylamine‐O‐sulfonic acids as inexpensive, readily available, and …

Rh( ii )-catalysed room temperature aziridination of homoallyl-carbamates - Chemical
Communications (RSC Publishing) DOI:10.1039/B611662K Royal Society of Chemistry View …

Due to their highly regio-and stereoselective ring-opening reactions, aziridines are valued
as building blocks for the synthesis of a wide range of nitrogen-containing compounds. 1 …

Intramolecular aziridination of alkenyl sulfonyliminoiodanes occurs thermally in the absence
of conventional metal catalysts such as Rh (II) and Cu (II). In rigid molecular systems …

N-functionalized aziridines, which are both useful intermediates and important synthetic
targets, can be envisioned as arising from the addition of nitrenes (ie., NR fragments) to …

Aziridination of alkenes is an important chemical transformation and is a convenient method
for accessing various nitrogen-containing products and synthetic intermediates.[1] …

Unactivated aziridines are the core substructures in a plethora of bioactive natural products
and serve as building blocks in organic synthesis. Despite this, very limited methods are …