886036-91-5

Upstream product

• 886036-90-4 1,6-bis-(tert-butyl-diphenyl-silanyloxy)-8-(2,5-dimethyl-hept-1-enyl)-7-methyl-9H-carbazole-4-carboxylic acid methyl ester 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 573693-08-0 2-bromo-4-methoxy-3-methyl-phenylamine 
• 573693-07-9 4-methoxycarbonyl-2-trifluoromethylsulfonyloxyanisole 
• 573693-12-6 3-(2-bromo-4-methoxy-3-methyl-phenylamino)-4-methoxy-benzoic acid methyl ester 
• 573693-17-1 8-bromo-1,6-dihydroxy-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 
• 573693-14-8 8-bromo-1,6-bis-(tert-butyl-diphenyl-silanyloxy)-7-methyl-9H-carbazole-4-carboxylic acid methyl ester 

Downstream Products

• 909708-78-7 3,8-bis-(tert-butyl-diphenyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-1-(2,5-dimethyl-hept-1-enyl)-2-methyl-9H-carbazole 
• 909708-80-1 3,8-bis-(tert-butyl-diphenyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-1-[3-methyl-3-(3-methyl-pentyl)-oxiranyl]-9H-carbazole 

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 and assignment of the absolute configuration of the neuronal cell protecting alkaloid carbazomadurin B

Using a palladium-catalyzed approach, the first enantio-selective synthesis of the neuronal cell protecting agent carbazomadurin B is described and its absolute configuration is assigned. Georg Thieme Verlag Stuttgart.