210489-77-3Relevant academic research and scientific papers
Preparation of a key tricyclic intermediate for the synthesis of pyrroloiminoquinone natural products
Kraus, George A.,Selvakumar, Natesan
, p. 845 - 846 (1998)
Indole 12 was prepared in seven steps from para-anisidine. The key step was an intramolecular nucleophilic aromatic substitution reaction.
Synthetic routes to pyrroloiminoquinone alkaloids. A direct synthesis of makaluvamine C
Kraus, George A.,Selvakumar, Natesan
, p. 9846 - 9849 (1998)
Makaluvamine C is a pyrroloiminoquinone which has been isolated from marine sponges. This molecule has been synthesized in 13 steps from p- anisidine. The key steps in this synthesis include an intramolecular nucleophilic aromatic substitution mediated by
