5472-84-4Relevant articles and documents
Convenient synthesis of 7H-Naphtho-[1,8-gh]quinolin-7-one
Sawada, Tadanobu,Ishii, Hiroyuki,Aoyama, Yoshitomo,Ueda, Toyotoshi,Aoki, Junji,Takekawa, Minoru
, p. 784 - 793 (2012)
7H-Naphtho[1,8-gh]quinolin-7-one was prepared by the glycerol condensation of 3-aminophenalenone in good yields. This method provides a new and convenient synthesis of the compound. NMR spectra of its related compounds were measured, and the rapid interchange between two equivalent a-enone structures was found, which is well known as the phenomenon for the formation of carboxylic acid dimer or hydrogen difluoride ion. Taylor & Francis Group, LLC.
Synthesis of Positional Isomeric Phenylphenalenones
Ospina, Felipe,Ramirez, Adrian,Cano, Marisol,Hidalgo, William,Schneider, Bernd,Otálvaro, Felipe
, p. 3873 - 3879 (2017/04/11)
A series of isomeric phenylphenalenones in which the phenyl ring is located at all possible peripheral positions of the phenalenone nuclei was synthesized. The structural characteristics of the series, in which topological variation is permitted with minimal electronic disturbance, could, in principle, allow for easy pharmacophore recognition when the compounds are aligned in steroidomimetic conformations.