1373350-91-4Relevant academic research and scientific papers
Intramolecular fischer indole synthesis and its combination with an aromatic [3,3]-sigmatropic rearrangement for the preparation of tricyclic benzo[cd]indoles
Park, In-Keol,Park, Jun,Cho, Cheon-Gyu
supporting information; experimental part, p. 2496 - 2499 (2012/04/18)
At the end of the tether: Aryl hydrazides that have carbonyl groups tethered at the para position of the aromatic ring undergo an intramolecular Fischer indolization reaction to give the corresponding indolophanes. Strategic insertion of a double bond in the tether enables a tandem aromatic [3,3] sigmatropic rearrangement reaction to occur to give tricyclic benzo[cd]indoles. Copyright
