1284280-22-3

Upstream product

• 645-13-6 4-isopropylacetophenone 
• 42139-37-7 1-isopropyl-4-(2-nitrovinyl)benzene 
• 142521-08-2 1,1-dibromo-2-(4-isopropylphenyl)ethene 

Relevant academic research and scientific papers

Copper(I) iodide-catalyzed synthesis of 4-aryl-1 H -1,2,3-triazoles from anti -3-aryl-2,3-dibromopropanoic acids and sodium azide

4-Aryl-1H-1,2,3-triazoles were synthesized from anti-3-aryl-2,3- dibromopropanoic acids and sodium azide by using inexpensive copper(I) iodide as the catalyst in dimethyl sulfoxide

Direct Synthesis of 4-Aryl-1,2,3-triazoles via I2-Promoted Cyclization under Metal- And Azide-Free Conditions

We herein report an iodine-mediated formal [2 + 2 + 1] cyclization of methyl ketones, p-toluenesulfonyl hydrazines, and 1-aminopyridinium iodide for preparation of 4-aryl-NH-1,2,3-triazoles under metal- and azide-free conditions. Notably, this is achieved

Method of catalytically synthesizing 4-aryl-NH-1,2,3-triazole derivative under microwave radiation

The invention discloses a method of catalytically synthesizing 4-aryl-NH-1,2,3-triazole derivative under microwave radiation. The method includes the steps of: successively adding substituted 2-nitroolefin, sodium azide, TfOH, and pyridine into a reaction

DABCO-mediated aza-Michael addition of 4-aryl-1H-1,2,3-triazoles to cycloalkenones. Regioselective synthesis of disubstituted 1,2,3-triazoles

Aza-Michael addition of 4-aryl-1H-1,2,3-triazoles to 2-cycloalken-1-ones has been studied in the presence of DABCO as organic base. The reactions were carried out in acetonitrile at room temperature to provide 2,4-disubstituted 2H-1,2,3-triazoles as major

Copper-catalyzed synthesis of 4-Aryl-1H-1,2,3-triazoles from 1,1-dibromoalkenes and sodium azide

A new methodology for the Cu-catalyzed synthesis of 1H-1,2,3-triazoles from 1,1-dibromoalkenes and sodium azide is presented. Aryl dibromoolefins were efficiently converted into the corresponding 1,2,3-triazoles. A comprehensive number of functional group