108320-76-9

Upstream product

• 100-11-8 1-bromomethyl-4-nitro-benzene 
• 21422-40-2 methyl 1H-indole-2-acetate 
• 91653-14-4 1-<2-(carbomethoxymethyl)-3-indolyl>-1-(3-pyridyl)ethene 
• 108320-73-6 3-[1-(2-Methoxycarbonylmethyl-1H-indol-3-yl)-vinyl]-1-(4-nitro-benzyl)-pyridinium; bromide 

Downstream Products

• 77251-57-1 11-methyl-6H-pyrido<4,3-b>carbazole-5-carbaldehyde 
• 108320-78-1 5-(hydroxymethyl)-11-methyl-6H-pyrido<4,3-b>carbazole 
• 108320-77-0 5-carbomethoxy-11-methyl-6H-pyrido<4,3-b>carbazole 
• 110527-58-7 2-(4-Dimethylamino-phenylamino)-11-methyl-2H-pyrido[4,3-b]carbazole-5-carboxylic acid methyl ester 
• 110547-49-4 2-(4-Amino-benzyl)-11-methyl-2,3,4,6-tetrahydro-1H-pyrido[4,3-b]carbazole-5-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Synthesis and Biological Properties of Some 6H-Pyridocarbazoles

The effect of methyl substitution on the biological properties of the ellipticines was reexamined. 9-Hydroxy-6H-pyridocarbazole was synthesized and shown to be devoid of antitumor activity in murine P388 lymphocytic leukemia in mice. 5-(Hydroxymeth

SYNTHESIS OF 5-HYDROXYMETHYL-11-METHYL-6H-PYRIDOCARBAZOLE AND 5-FORMYL-11-METHYL-6H-PYRIDOcarbazole (17-OXOELLIPTICINE)

A synthesis of 5-hydroxymethyl-11-methyl-6H-pyridocarbazole and the corresponding 5-formyl derivative, 17-oxoellipticine, is described, the key feature of which is the use of the Krohnke aldehyde synthesis to effect the debenzylation of a p-nitrobe