682753-67-9

Upstream product

• 682753-62-4 (S)-2-{[1-(tert-butyl-dimethylsilyl)-1H-indol-4-yl]-methylamino}-3-methyl-butyric acid benzyl ester 
• 5192-23-4 4-amino-1H-indole 
• 606-20-2 2,6-dinitrotoluene 
• 78283-21-3 3-nitro-trans-2-[β-(dimethylamino)vinyl]-nitrobenzene 
• 682753-54-4 (S)-2-(1H-indol-4-ylamino)-3-methyl-butyric acid benzyl ester 
• 682753-58-8 (S)-2-[1-(tert-butyl-dimethylsilyl)-1H-indol-4-ylamino]-3-methyl-butyric acid benzyl ester 

Relevant academic research and scientific papers

A Regioselective Acylation of N-Substituted-4-Aminoindole. Its Application to the Synthesis of Indolactam V

Optically active (-) Indolactam V (1) was formally synthesized with the defined stereochemistry, through an efficient procedure via bromationlithiation in the 3-position of the indole ring using 2,6-dinitrotoluene and the aminoacids: D-serine and D-valine