1000683-03-3

Upstream product

• 1000682-81-4 1-benzyl-3-(1-phenyl-2-phenylselenoethyl)-1H-indole 
• 1616477-47-4 1-(1-benzyl-1H-indol-3-yl)-1-phenylethanol 
• 1589-82-8 phenylmagnesium bromide 
• 93315-38-9 3-acetyl-1-benzyl-1H-indole 

Relevant academic research and scientific papers

A highly efficient route to C-3 alkyl-substituted indoles via a metal-free transfer hydrogenation

A highly efficient route to C-3 alkyl-substituted indoles via completely metal-free catalytic transfer hydrogenation of 3-indolemethanols was developed. This process proceeds via vinylogous iminium intermediates formed in situ in the presence of Br?nsted

Novel Bronsted acid catalyzed three-component alkylations of indoles with N-phenylselenophthalimide and styrenes

(Chemical Equation Presented) Novel and efficient Bronsted acid (p-TsOH) catalyzed inter- and intramolecular Friedel-Crafts alkylations have been developed to synthesize selenated three-component coupling and selenation-cyclization indole derivatives. Chemical removal of the phenylseleno moiety was investigated, and the reaction mechanisms were discussed.