42153-74-2

Upstream product

• 205581-06-2 S-methyl-S-phenyl-N-(p-tolylsulfonyl)sulfimide 
• 82754-04-9 C₁₄H₁₄BrNO₃S₂ 
• 4381-25-3 S-methyl-S-phenylsulfoximine 
• 98-59-9 p-toluenesulfonyl chloride 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 1193-82-4 racemic methyl phenyl sulfoxide 
• 70-55-3 toluene-4-sulfonamide 
• 100-68-5 methyl-phenyl-thioether 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 4381-25-3 (S)-S-methyl-S-phenylsulfoximine 
• 1338062-05-7 4-methyl-N-[(2-propoxyphenyl)-λ³-iodanylidene]benzenesulfonamide 
• 82753-99-9 C₁₄H₁₂Br₃NO₃S₂ 
• 36744-90-8 S,S-Diphenylsulfilimine 
• 89538-92-1 N-(4-methylbenzenesulfonyl) phenyl sulfonimidoyl chloride 

Downstream Products

• 82753-99-9 C₁₄H₁₂Br₃NO₃S₂ 
• 82753-94-4 C₁₄H₁₂Cl₃NO₃S₂ 
• 104449-90-3 C₁₄H₁₄INO₃S₂ 
• 147383-20-8 S-((E)-prop-1-enyl)-S-phenyl-N-(p-tolylsulfonyl)sulfoximide 
• 147297-64-1 S-<(E)-Pent-1-enyl>-S-phenyl-N-(p-tolylsulfonyl)sulfoximine 
• 110814-66-9 S-(2-Methoxy-2-oxoethyl)-S-phenyl-N-(p-tolylsulfonyl)sulfoximine 
• 89279-68-5 S-phenyl-N-(p-tolylsulfonyl)-S-vinylsulfoximide 
• 67087-38-1 S-Chlormethyl-S-phenyl-N-(p-tolylsulfonyl)-sulfoximin 
• 82754-02-7 C₁₄H₁₃Cl₂NO₃S₂ 
• 1200799-53-6 C₁₈H₁₉NO₄S₂ 
• 917792-43-9 C₁₈H₁₉NO₄S₂ 

Relevant academic research and scientific papers

I2-Catalyzed N-Sulfonylation of Sulfoximines with Sulfinates in Water at Room Temperature

An oxidative coupling of NH-sulfoximines and arylsulfinates catalyzed by of I2 and H2O2 affords N-sulfonyl sulfoximines. The reaction proceeds under aerobic conditions in water at room temperature. The merits of this proto

Copper-catalyzed imination of sulfoxides and sulfides

Sulfoximines and sulfilimines have attracted considerable interest among organic chemists. The Cu(II)-catalyzed imination of sulfoxides and sulfides using various N-fluoro benzenesulfonamides was investigated in this study. The scope of the reaction was demonstrated by using several substituted sulfides and sulfoxides. The flow strategy for the preparation of NH-sulfoximines was also examined. By trapping nitrene intermediates through triphenylphosphine, we found that the reaction was conducted through a metal-nitrene intermediate mechanism.

Synthetic method of N-aryl sulfone sulfoximine

Sulfoximines have a wide range of applications in organic chemistry, medicinal chemistry, agricultural chemistry, sulfimides are related to the medicinal activity of various organisms, such as antiarrhythmic, antispasmodic, antiasthmatic and antiviral act

Iron-catalyzed imidative kinetic resolution of racemic sulfoxides

Kinetic resolution of racemic sulfoxides requires either custom substrates or shows moderate enantioselectivity, leading to achiral coproducts (such as sulfones) as an intrinsic part of the process. A new strategy is demonstrated that allows the resolution of racemic sulfoxides through catalytic asymmetric nitrene-transfer reactions. This approach gives rise to both optically active sulfoxides and highly enantioenriched sulfoximines. By using a chiral iron catalyst and a readily available iodinane reagent, high selectivity factors have been achieved under very practical reaction conditions. With respect to the substrate scope, it is noteworthy that this unprecedented imidative kinetic resolution of racemic sulfoxides provides access to both aryl-alkyl and dialkyl sulfoximines in highly enantioenriched forms. Copyright

O-alkoxyphenyliminoiodanes: Highly efficient reagents for the catalytic aziridination of alkenes and the metal-free amination of organic substrates

Efficient nitrene precursors: Highly reactive iminoiodane-based nitrene precursors were prepared from ortho-alkoxyiodobenzenes. Owing to the presence of the ortho-substituent on the phenyl ring, these new iminoiodanes have excellent solubility in organic

A versatile and highly reactive polyfluorinated hypervalent iodine (III) compound

(Figure Presented) Hyper-reactive: A highly reactive, fully fluorinated hypervalent iodine reagent (see formula) mediates new transformations (e.g. the one-pot conversion of sulfides to sulfoximines) and serves as a stoichiometric oxidant in well-established reactions (e.g. C-C bond cleavage and the conversion of alcohols into aldehydes).

Transannular, decarboxylative Claisen rearrangement reactions for the synthesis of sulfur-substituted vinylcyclopropanes

Unsaturated ε-lactones bearing an α-arylsulfonyl or α-arylsulfoximinyl substituent undergo stereoselective transannular, decarboxylative Claisen rearrangement to give substituted vinylcyclopropanes.

Synthesis of phosphanyl sulfoximines through phospha-michael reaction of alkenyl sulfoximines and their evaluation as chiral bidentate 1, 5-N, P ligands for palladium in asymmetric allylic alkylation

The intermolecular phospha-Michael reaction of cyclic and acyclic alkenyl sulfoximines proceeds readily and yields the corresponding phosphanyl sulfoximines in good yield. The asymmetric induction provided, by sulfoximine group in C-P bond formation is ap

Iron(ii) triflate as an efficient catalyst for the imination of sulfoxides

The challenging imination of benzyl-, sterically demanding alkyl-, and heteroaryl-substituted sulfoxides has been studied. Iron(II) triflate was identified as a highly efficient and robust catalyst for sulfur imination reactions. A variety of sulfoxides a

Iron-catalyzed imination of sulfoxides and sulfides

The Fe(III)-catalyzed imination of sulfoxides and sulfides with sulfonylamides in the presence of iodinanes has been investigated. The best results were obtained when Fe(acac)3 was used as a catalyst in combination with iodosylbenzene, providin