824390-92-3

Upstream product

• 863401-20-1 (E)-N-(3-bromobenzylidene)-4-methylbenzenesulfonamide 
• 908131-20-4 3-(3-bromo-phenyl)-3-(toluene-4-sulfonylamino)-propionic acid tert-butyl ester 
• 908131-25-9 N-[1-(3-bromo-phenyl)-3-hydroxy-propyl]-4-methyl-benzenesulfonamide 
• 824390-89-8 4-methyl-N-(1-(3-bromophenyl)-allyl)-benzenesulfonamide 

Downstream Products

• 1000979-71-4 (E)-3-(3-bromophenyl)-N-tosylprop-2-en-1-amine 
• 1000979-73-6 1-(3-bromophenyl)-3-(tosylamino)propan-1-one 
• 824391-04-0 C₂₃H₂₁BrN₂O₂S 
• 1133016-31-5 C₁₈H₁₉BrN₂O₂S 
• 1202798-86-4 N-(3-(3-bromophenyl)-3-chloropropyl)-4-methylbenzenesulfonamide 

Relevant academic research and scientific papers

A convenient synthetic route to 2-aryl-N-tosylazetidines and their ZnX2 (X = I, OTf) mediated regioselective nucleophilic ring opening reactions: synthesis of γ-iodoamines and tetrahydropyrimidines

A general and convenient synthetic route to various 2-aryl-N-tosylazetidines has been described. Their ZnX2 (X = I, OTf) mediated nucleophilic ring opening with halides and [4+2] cycloaddition reactions with various nitriles have been achieved

2-Aryl-N-tosylazetidines as formal 1,4-dipoles for [4 + 2] cycloaddition reactions with nitriles: An easy access to the tetrahydropyrimidine derivatives

(Chemical Equation Presented) A new synthetic route to 2-aryl-N-tosyl azetidines has been developed starting from N-tosylarylaldimines in two steps in an overall yield of 63-70%. A formal [4 + 2] cycloaddition of these 2-aryl-N-tosylazetidines with nitril