573693-15-9

Upstream product

• 573693-09-1 C₂₀H₄₂Sn 
• 573693-14-8 8-bromo-1,6-bis-(tert-butyl-diphenyl-silanyloxy)-7-methyl-9H-carbazole-4-carboxylic acid methyl ester 
• 573693-13-7 8-bromo-1,6-dimethoxy-7-methyl-9H-carbazole-4-carboxylic acid methyl ester 
• 573693-17-1 8-bromo-1,6-dihydroxy-7-methyl-9H-carbazole-4-carboxylic acid methyl ester 
• 573693-12-6 3-(2-bromo-4-methoxy-3-methyl-phenylamino)-4-methoxy-benzoic acid methyl ester 
• 6702-50-7 3-hydroxy-4-methoxybenzoate 
• 2203-80-7 5-methylhex-1-yne 
• 573693-10-4 1-iodo-2,5-dimethylhex-1-ene 
• 573693-07-9 4-methoxycarbonyl-2-trifluoromethylsulfonyloxyanisole 
• 573693-11-5 2-bromo-4-methoxy-3-methyl-1-nitro-benzene 
• 573693-08-0 2-bromo-4-methoxy-3-methyl-phenylamine 
• 55289-35-5 2-bromo-6-nitrotoluene 
• 7766-23-6 3-bromo-2-methylphenol 
• 31804-36-1 1-bromo-3-methoxy-2-methylbenzene 

Relevant academic research and scientific papers

Transition metals in organic synthesis - Part 83#: Synthesis and pharmacological potential of carbazoles

A series of carbazole derivatives with promising pharmacological properties has been prepared using either an iron-mediated or a palladium-catalyzed synthetic approach. The carbazole alkaloids carbazoquinocin C, carbazomadurin A and B, epocarbazolin A and

First total synthesis of the neuronal cell protecting carbazole alkaloid carbazomadurin A by sequential transition metal-catalyzed reactions

The highly oxygenated neuronal cell protecting carbazole alkaloid carbazomadurin A was synthesized in nine steps and 11% overall yield from isovanillic acid.