41411-59-0

Upstream product

• 135908-05-3 2-hydroxy-3-chloropropyl p-toluenesulfonate 
• 96-13-9 2,3-Dibromopropan-1-ol 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 64-17-5 ethanol 
• 106-89-8 epichlorohydrin 

Downstream Products

• 95924-42-8 acetoxy-1 p-toluenesulfonyl-3 propene-2 
• 78473-63-9 (3-chloro-propenyl)-p-tolyl sulfone 
• 103038-44-4 3-bromo-1-(p-tolylsulfonyl)propene 
• 7497-34-9 2,5-bis-(toluene-4-sulfonylmethyl)-[1,4]dioxane 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 3112-87-6 1-methyl-4-(prop-2-ene-1-sulfonyl)benzene 
• 28151-59-9 (Z)-1-chloro-3-(p-tolylsulfonyl)propene 
• 28005-38-1 2-ethoxy-1-chloro-3-(toluene-4-sulfonyl)-propane 
• 95526-68-4 (3-iodo-propenyl)-p-tolyl sulfone 
• 103755-51-7 (1-phenyl-1H-1,2,3-triazol-5-yl)methanol 
• 90323-90-3 [3-(4-nitro-phenyl)-3H-[1,2,3]triazol-4-yl]-methanol 
• 77177-16-3 1-(benzyl)-5-hydroxymethyl-1H-1,2,3-triazole 

Relevant academic research and scientific papers

A general route to 1,5-disubstituted 1,2,3-triazoles with alkyl/alkyl, alkyl/aryl, aryl/aryl combinations: A metal-free, regioselective, one-pot three component approach

An experimentally simple one-pot reaction, affording 1,5-disubstituted 1H-1,2,3-triazoles in good to excellent yields by combining vinyl sulfones, sodium azide and alkyl bromides, -tosylates, -mesylates or aryl amines, -iodides is reported. The organic az