74861-95-3Relevant academic research and scientific papers
PYRROLOINDOLES. 2. SOME ELECTROPHILIC SUBSTITUTION REACTIONS IN THE 1H,6H-PYRROLOINDOLE SERIES
Samsoniya, Sh. A.,Targamadze, N. L.,Kurkovskaya, L. N.,Kereselidze, Dzh. A.,Suvorov, N. N.
, p. 495 - 500 (2007/10/02)
As expected, the 3 and 8 positions are the reaction centers of 1H,6H-pyrroloindole in the Vilsmeier-Haack and Mannich reactions.Diazo coupling takes place primarily in the 3 position and leads primarily to monosubstitution products. 6,8-Diacetyl-1H,6H-pyrroloindole and 1,8-diacetyl-1H,6H-pyrroloindole were isoleted from the acetylation products.
