150810-82-5Relevant academic research and scientific papers
Condensation des Indoles sur la 5-Hydroxy-1,4-naphthoquinone (Juglone). Synthese d'une Nuvelle Serie de 3,8-Diindolyl-5-hydroxy-1,4-naphthoquinones et de la Premiere 3,6,8-Triindolyl-5-hydroxy-1,4-naphthoquinone
Henrion, Jean-Christophe,Jacquet, Bernard,Hocquaux, Michel,Barre, Gille,Hedayatullah, Mir,Lion, Claude
, p. 409 - 414 (2007/10/03)
Indoles unsubstituted in the 3 position react with 5-hydroxy-1,4-naphthoquinone (juglone) to yield 3-(3-indolyl)-5-hydroxy-1,4-naphthoquinone (3,8-diindolyl)-5-hydroxy-1,4-naphthoquinone.This two-step mechanism makes it possible to obtain the disubstituted juglones with differently substituted indolyl residues.It was also possible to prepare a new 3,6,8-triindolyljuglone.
