14561-75-2

Upstream product

• 98-10-2 benzenesulfonamide 
• 124-63-0 methanesulfonyl chloride 

Relevant academic research and scientific papers

Production of aromatic sulfonimide compounds

[A] a variety of substrate, adsorbing agent using a new, safely and conveniently, sulfonimide aromatic compound to a method. [Solution] R a-H [formula, R is a substituted or unsubstituted aryl groups, or substituted or unsubstituted heteroaryl group. ] Is represented by the aromatic compound,[In the formula, Ar1 And Ar2 The same or different, substituted or unsubstituted alkyl groups, substituted or unsubstituted aryl groups, or substituted or unsubstituted heteroaryl group. ]In the radiosensitive compound represented by the composition, in the presence of an oxidizing agent is irradiated with light. [Drawing] no

Sulfonimidation via ring-opening of 2-oxazolines with acidic sulfonimide nucleophiles

Acidic sulfonimide nucleophiles including dibenzenesulfonimide, o-benzenesulfonimide, dimethanesulfonimide, and N-(methylsulfonyl)-benzenesulfonamide are discovered to open a variety of alkyl-, aryl- and heteroaryl-2-oxazoline rings to provide the sulfonimidation products in refluxing 1,4-dioxane. The electron-rich 2-oxazoline substrates worked well for the nucleophilic ring-opening reactions while no reaction took place for the electron-poor 2-oxazoline substrates.

Polysulfonylamines, LXIII. Methanol as a Link in 18-Crown-6-Complexes with Uncharged Acidic Molecules: Syntheses and Crystal Structures of Two Monomeric Complexes (CH2CH2O)6*2MeOH*2HN(SO2-Aryl)2 and of the Chain-Polymeric Complex <(CH2CH2O)6*3MeOH*HN(SO2M

The thermally labile ternary complexes 18C6*2MeOH*2HN(SO2Ph)2 (2a), 18C6*2MeOH*2HN(SO2-C6H4-4-Cl)2 (2b) and 18C6*3MeOH*HN(SO2Me)(SO2Ph) (3) were obtained by co-crystallization of 18-crown-6 (18C6) and the appropriate di(organosulfonyl)amine from methanoli