338777-79-0

Upstream product

• 583-55-1 1-Bromo-2-iodobenzene 
• 1433218-62-2 C₁₆H₁₈INO₅S₂ 
• 1433218-61-1 C₂₂H₂₂INO₅S₂ 
• 1433218-60-0 C₁₅H₁₅ClINO₂S 
• 1433218-59-7 N-(2-iodoethyl)-N-(2-iodophenyl)-4-methylbenzenesulfonamide 
• 1427218-61-8 C₁₅H₁₅BrINO₂S 
• 61613-20-5 N-tosyl-2-iodoaniline 
• 615-43-0 2-iodophenylamine 
• 1420043-07-7 C₁₅H₁₆INO₂S₂ 
• 1420043-16-8 C₁₇H₁₈INO₃S₂ 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 3080-99-7 3,4-dihydro-2H-benzo[1,4]thiazine 
• 1433218-57-5 C₁₅H₁₅NO₃S₂ 
• 1433218-58-6 C₁₅H₁₅NO₄S₂ 

Relevant academic research and scientific papers

N-Tosyl-1,5,2,6-dithiadiazocane: A waste-free electrophilic sulfur reagent for the efficient synthesis of medium-ring S,N-heterocycles

We report on the application of an eight-membered C2-symmetric sulfenamide derivative as a new convenient and highly reactive electrophilic sulfur-nucleophilic nitrogen synthon for the concise synthesis of medium-ring S,N-heterocyclic systems.

Efficient access to 1,4-benzothiazine: Palladium-catalyzed double C-S bond formation using Na2S2O3 as sulfurating reagent

A novel Pd-catalyzed double C-S bond formation coupling reaction has been developed. This protocol, in which Na2S2O3 was used as sulfurating reagent in metal-catalyzed reactions, provides an efficient method for the synthe

Nickel-mediated inter- and intramolecular C-S coupling of thiols and thioacetates with aryl iodides at room temperature

A Ni(0)-catalyzed intermolecular cross-coupling of various functionalized thiols and aryl iodides has been developed and successfully extended to less explored intramolecular versions, where thioacetates could also be utilized as the strategic surrogate. Air-stable precatalysts, very mild conditions, and an easy protocol allow rapid access to medicinally useful aryl thioethers, as demonstrated in the facile synthesis of (±)-chuangxinmycin as a key step.