1312680-91-3

Upstream product

• 1152979-96-8 4-(trifluoromethyl)benzenesulfonyl azide 
• 536-74-3 phenylacetylene 
• 2991-42-6 4-trifluorophenylsulfonyl chloride 

Downstream Products

• 1312681-07-4 (S)-(-)-N-(2-cyclohexyl-2-phenylethyl)-4-(trifluoromethyl)benzenesulfonamide 
• 7695-69-4 bis(phenylthio)methylbenzene 
• 77815-78-2 1,1-bis(phenylthio)-1,2-diphenylethane 
• 451-40-1 phenyl benzyl ketone 
• 1613045-88-7 (Z)-N-(1-(dimethylamino)-3-oxo-1,3-diphenylprop-1-en-2-yl)-4-(trifluoromethyl)benzenesulfonamide 
• 1613045-89-8 C₂₄H₂₁F₃N₂O₃S 

Relevant academic research and scientific papers

Synthesis of 2-Bromoimidazoles from Alkynes, N-Sulfonylazides, and Bromocyanides

(Chemical Equation Presented) A synthetic method for 2-bromoimidazoles is developed from Rh-catalyzed cyclization of N-sulfonyl-1,2,3-triazoles with bromocyanides. Cu-catalyzed [3 + 2] cycloaddition followed by Rh-catalyzed cyclization starting from alkyn

Synthesis of benzothiazonine by rhodium-catalyzed denitrogenative transannulation of 1-sulfonyl-1,2,3-triazole and thiochromone

A facile synthesis of multi-functionalized benzothiazonine was achieved by the rhodium-catalyzed denitrogenative annulation of 1-sulfonyl-1,2,3-triazole and thiochromone. In view of the excellent atom economy, broad substrate scope and easy availability of starting materials, the protocol provided an efficient strategy for the construction of mediumN,S-heterocycles.

METHOD OF PRODUCING SULFONYL OR SULFAMOYL TRIAZOLE-BASED COMPOUNDS USING CONTINUOUS FLOW PROCESS

The present invention relates to a method for manufacturing a sulfonyl or sulfamoyl triazole-based compound using a continuous flow process. According to embodiments of the present specification, the sulfonyl or sulfamoyl triazole-based compound frequentl

Catalytic asymmetric C-H insertions of rhodium(II) azavinyl carbenes

A highly efficient enantioselective C-H insertion of azavinyl carbenes into unactivated alkanes has been developed. These transition metal carbenes are directly generated from readily available and stable 1-sulfonyl-1,2,3-triazoles in the presence of chiral Rh(II) carboxylates and are used for C-H functionalization of alkanes to access a variety of β-chiral sulfonamides.