1310690-01-7Relevant academic research and scientific papers
Synthesis of substituted indolizino[8,7-b]indoles from harmine and their biological activity
Nurmaganbetov, Zh. S.,Shultz,Chernov,Turmukhambetov, A. Zh.,Seydakhmetova,Shakirov,Tolstikov,Adekenov
, p. 1494 - 1499 (2012/01/06)
The reaction of harmine with phenacyl bromides or ethyl bromoacetate gives quaternized harmine derivatives. The cyclization of the phenacylharminium salts yields the corresponding 2-aryl-11H-indolizino[8,7-b]indoles. Vilsmaier-Haack formylation of 11H-ind
