295316-03-9Relevant academic research and scientific papers
Regiocontrolled annellation reactions starting from diethoxymethyl protected indole
Kraxner, Johannes,Gmeiner, Peter
, p. 1081 - 1083 (2007/10/03)
Directed metallation of the diethoxymethyl protected indole 4 followed by treatment with β-nitrostyrene leads to the 1,2- disubstituted indole 5. Using 5 as a central intermediate, the tricyclic annellation products of type 2 and 3 were accessed when the regiochemical outcome of the reactions could be controlled.
