331973-76-3

Upstream product

• 114049-59-1 (9H-carbazol-9-yl)(2-chlorophenyl)methanone 
• 86-74-8 9H-carbazole 
• 88-65-3 2-bromobenzoic-acid 
• 866594-44-7 9-(4-chloro-3-pyridinecarbonyl)carbazole 
• 866594-50-5 9-(4-bromo-3-pyridinecarbonyl)carbazole 
• 866594-45-8 9-(3-bromo-2-pyridinecarbonyl)carbazole 
• 866594-40-3 9-(3-bromo-4-pyridinecarbonyl)carbazole 
• 866594-42-5 9-(2-chloro-3-pyridinecarbonyl)carbazole 

Relevant academic research and scientific papers

TFAA/H3PO4 mediated unprecedented N-acylation of carbazoles leading to small molecules possessing anti-proliferative activities against cancer cells

For the first time TFAA/H3PO4 has facilitated the direct and metal-free N-acylation of carbazoles leading to a number of N-acylated derivatives. Several of these compounds were found to be promising when tested for their anti-proliferative properties against oral cancer cell lines. This journal is the Partner Organisations 2014.

A versatile route to benzocanthinones

Benzocanthinone (1) and five analogs (10, 12-15) were prepared by radical-induced cyclizations of halo N-aroyl derivatives of β-carboline and carbazole.