1350896-34-2Relevant 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
Dey, Santu,Pathak, Tanmaya
, p. 9275 - 9278 (2014/03/21)
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
A metal-free, aqueous and general route to 1,5-disubstituted-1,2,3- triazoles: "Reversed regioisomeric" 1,3-dipolar cycloaddition of azides and vinyl sulfones
Dey, Santu,Datta, Dhrubajyoti,Pathak, Tanmaya
, p. 2521 - 2524 (2011/12/01)
A metal-free, vinyl sulfone-based synthesis of 1,5-disubstituted-1,2,3- triazoles is reported for the first time. These triazoles are easily formed in a regioselective fashion by heating under reflux a mixture of a substituted vinyl sulfone and an organic
