91668-35-8Relevant academic research and scientific papers
An efficient, general synthesis of 2-substituted 3,6-dihydropyrrolo[3,2-e] indoles involving one-pot Sonogashira coupling and cyclisation
Rakshit, Moumita,Kundu, Taraknath,Kar, Gandhi K.,Chakrabarty, Manas
, p. 717 - 724 (2013/07/26)
A number of 2-substituted 3,6-dihydropyrrolo[3,2-e]indoles were synthesised efficiently by the reaction of 4-iodo-1-(phenylsulfonyl)-5-(trifluoroacetamido) indole with terminal acetylenes in the presence of a palladium(0) catalyst and a copper(I) co-catal
PYRROLOINDOLES. 10. SYNTHESIS OF SOME SUBSTITUTED PYRROLOINDOLES
Samsoniya, Sh. A.,Kadzhrishvili, D. O.,Gordeev, E. N.,Suvorov, N. N.
, p. 376 - 379 (2007/10/02)
The formation of linear four-ring pyrrolocarbazole systems is observed in the indolization of cyclohexanone 1-acetyl-5-indolinyl- and 1-acetyl-6-indolinylhydrazones, whereas the formation of mixtures of linear and angular pyrroloindoles is observed in the
