504407-76-5

Upstream product

• 1224876-20-3 C₁₅H₁₂IN 
• 615-43-0 2-iodophenylamine 
• 4392-24-9 3-bromo-1-phenyl-1-propenyl bromide 

Downstream Products

• 1164108-90-0 1-methyl-3-(1-phenylprop-2-en-1-yl)-1H-indole 
• 1620878-68-3 1-benzyl-3-(1-phenylprop-2-en-1-yl)-1H-indole 

Relevant academic research and scientific papers

Insertion Reaction of 2-Halo- N -allylanilines with K 2S Involving Trisulfur Radical Anion: Synthesis of Benzothiazole Derivatives under Transition-Metal-Free Conditions

A synthesis of benzothiazole derivatives through the reaction of 2-halo- N -allylanilines with K 2S in DMF is developed. The trisulfur radical anion S 3· -, which is generated in situ from K 2S in DMF, initiates

Rhenium-Catalyzed Intramolecular Carboalkoxylation and Carboamination of Alkynes for the Synthesis of C3-Substituted Benzofurans and Indoles

A rhenium-catalyzed carboalkoxylation and carboamination of alkyne is reported. This reaction provides an efficient route to synthesize de novo C3-substituted benzofurans and indoles under mild conditions in moderate to good yields. Mechanistic studies re

Exclusive chemoselective reduction of imines in the coexistence of aldehydes using AuNPore catalyst

Aldimines (R1HC=NR2) were reduced in the coexistence of aldehydes (R1CHO) with 100% chemoselectivity by the use of AuNPore giving corresponding amines (R1H2C-NHR2) in high chemical yields.