1263383-14-7

Upstream product

• 124293-81-8 1-(benzenesulfonyl)-2-methyl-1H-indole-3-carbaldehyde 
• 493-09-4 benzo-1,4-dioxane 
• 1332607-78-9 [2-methyl-1-(phenylsulfonyl)-1H-indol-3-yl]methanediyl diacetate 
• 1273320-49-2 C₂₀H₁₈BrNO₆S 

Relevant academic research and scientific papers

Studies on Lewis-acid mediated domino reaction of N-protected bromomethylindoles with arenes/heteroarenes

A systematic study on Lewis-acid mediated domino reaction of N-protected 2/3-bromomethylindoles with various types of arenes and heteroarenes is reported.

Lewis acid mediated one-pot synthesis of aryl/heteroaryl-fused carbazoles involving a cascade Friedel-Crafts alkylation/electrocyclization/aromatization reaction sequence

A Lewis-acid-mediated domino reaction of 2/3-(bromomethyl)indoles with arenes/heteroarenes led to the formation of the corresponding annulated carbazoles. This three-step one-pot transformation proceeds by sequential Lewis acid catalysed Friedel-Crafts alkylation, electrocyclization and aromatization reactions. The strategy is highly efficient for the assembly of complex aryl/heteroaryl-fused carbazoles.